lunedì 23 marzo 2020

POLMONITE E TERAPIE

fonte: LIFEEXTENSION,  Sito: https://www.lifeextension.com/protocols/infections/pneumonia

Summary and Quick Facts
  • Pneumonia is a lung infection. It causes cough, shortness of breath and fever. It can progress to severe breathing problems, especially in older people or people with suppressed immune systems.
  • This protocol will teach you about the causes of pneumonia and how the condition typically progresses. Learn what treatments are available and what steps to take to reduce the risk of getting pneumonia.
  • Since common infections like colds may progress to pneumonia, supplements like probiotics and Reishi mushroom, which help support immune function, may help reduce pneumonia risk. N-acetylcysteine (NAC) has been shown to improve inflammatory markers in people with pneumonia.
Pneumonia is an infection of the lungs that can cause cough, trouble breathing, and fever, with possible severe complications such as respiratory failure. In the United States, pneumonia is the sixth leading cause of death in people 65 and older, and causes about one million hospitalizations each year.
Fortunately, several integrative interventions such as pu-erh tea, cistanche, zinc, vitamin D, and probiotic supplements may help fortify the body’s defenses against infections like pneumonia.

Causes

  • Pneumonia is caused primarily by infectious organisms.
  • If immune defenses are impaired (as occurs with age-related immune senescence), then pathogens are more likely to establish an infection.

Risk Factors

Note: Proton-pump inhibitors are normally used to suppress stomach acidity for relief of gastroesophageal reflux. They may be a particularly problematic risk factor for pneumonia because their use is widespread and those taking them may be unaware that they are associated with significantly increased pneumonia risk.

Signs and Symptoms

  • Fever and chills
  • Chest or abdominal pain
  • Pain with breathing, shortness of breath
  • Cough, dry or with phlegm; cough producing green or yellow sputum
  • Night sweats
  • Rapid heart and breathing rate

Diagnosis

Diagnosis is typically based on medical history, physical exam, chest X-ray, and a complete blood count.

Treatment

  • Antibiotics are the mainstay of bacterial pneumonia treatment.
  • Adjunctive corticosteroids may improve outcomes and reduce complication risk
  • Vaccines targeting pneumococcal and influenza infections are the cornerstone of prevention.

Novel and Emerging Strategies

  • Using antibiotics for a short amount of time and not using them for viral infections may reduce the risk of inducing resistance.
  • A study on pneumonia patients admitted to a hospital showed that those who were chronic aspirin users were about half as likely to die within 30 days of hospital admission as those not taking aspirin.
  • The use of statins has been associated with decreased risk of pneumonia and pneumonia-related death, as well as reduced rates of acute bacterial infections.

Diet and Lifestyle Considerations

One of the most important ways to avoid pneumonia is to keep the immune system functioning normally.
  • Avoid smoking and excessive alcohol consumption.
  • Eat a nutrient-dense diet rich in unprocessed whole plant-based foods.
  • Exercise is thought to activate immune cells, help expel bacteria from the airways, and reduce stress.
  • Regular hand washing is recommended as a strategy for avoiding respiratory infections.
  • Maintain good oral health, because harmful bacteria in the mouth can be drawn into the lungs and cause infection.

Integrative Interventions

  • Probiotics: Probiotics may prevent hospital-acquired pneumonia in critically ill patients and lessen the incidence and duration of upper respiratory tract infections in healthy adults and children.
  • Vitamin D: People with the lowest vitamin D levels were 2.6 times more likely to develop pneumonia compared with those with the highest vitamin D levels in a study that followed older people for nearly 10 years.
  • Zinc: In a one-year study, nursing home residents with lower zinc status had almost twice the risk of pneumonia as those with normal zinc status.
  • Cistanche: Cistanche deserticola has been used historically in traditional Chinese medicine to stimulate immunity in the elderly.
  • Pu-erh tea: Pu-erh tea was found to enhance immune cell number while decreasing the inflammatory cytokine interleukin-6 in mice with immune senescence.

2 Introduction

Pneumonia is a potentially serious infection of the lungs that can cause cough, trouble breathing, and fever, with possible severe complications such as respiratory failure (Mayo Clinic 2015; Musher 2012; UMMC 2012). In the United States, pneumonia is the sixth leading cause of death in people 65 and older, and causes about one million hospitalizations each year (Musher 2012; Torres 2013; American Thoracic Society 2015).
The immune system weakens with age, a phenomenon known as immune senescence (Murray 2015). This leaves older individuals increasingly vulnerable to the bacteria and viruses that cause most cases of pneumonia (Krone 2014; Mayo Clinic 2015; Musher 2012). People with underlying medical conditions, such as chronic lung disease or heart disease, are also at increased risk (Torres, Peetermans 2013; Mayo Clinic 2015). 
Antibiotics are the primary treatment for pneumonia and should be initiated when bacterial pneumonia is deemed probable (Musher 2012; Torres 2013). However, general overuse of antibiotics has driven the growing problem of antibiotic resistance, which can complicate pneumonia treatment (UMMC 2012). Pneumonia caused by drug-resistant bacteria is harder to treat and may lead to longer illness and greater risk of death (Bosso 2011).
Novel antibiotics and strategies to promote judicious antibiotic use, as well as campaigns to encourage broad uptake of pneumococcal vaccines among those 65 and older, are helping keep antibiotic resistance at bay to some degree. Nevertheless, innovative ways to prevent and manage infectious diseases like pneumonia are sorely needed (CDC 2015; Bosso 2011; Pinzone 2014). 
Intriguing recent studies suggest an association between cholesterol-lowering statin drugs and reduced risk of pneumonia and pneumonia-related death, and adjunctive corticosteroids have been shown to reduce pneumonia severity (Nassaji 2015; Cheng 2014; Marti 2015; Horita 2015; Siemieniuk 2015). Also, history of aspirin use has been associated with reduced risk of death within 30 days of hospital admission with pneumonia (Falcone 2015).
In addition, several integrative interventions such as reishi mushroom (Lin 2005), pu-erh tea (Zhang 2012), cistanche (Wu 2005; Yamada 2010; Zhang 1988; Zhang 2014), zinc (Barnett 2010), vitamin D (Youssef 2012), and probiotic supplements (Hao 2015) may help fortify the body’s defenses against infections like pneumonia. 
In this protocol you will learn about the causes of pneumonia and how this potentially fatal respiratory disease is typically managed. You will read about risk factors that could increase your vulnerability to pneumonia, and what lifestyle and dietary habits can help reduce your risk. Several novel and emerging pneumonia prevention and treatment strategies will be reviewed, and a number of natural interventions that may help mitigate pneumonia risk will be described. Given the significant contribution of immune senescence to pneumonia risk in the elderly, aging individuals should also review the Immune Senescence protocol.

3 Causes And Risk Factors


Pneumonia is caused primarily by infectious organisms. Pathogens can reach the lungs through inhalation of atmospheric air or can originate in secretions of the upper airways, which travel to the lungs. Rarely, microbes from other parts of the body move to the lungs via the bloodstream (Musher 2012). Although the lungs are constantly exposed to microbes, immune defenses usually prevent infection. However, if immune defenses are impaired (as occurs with age-related immune senescence), then pathogens are more likely to establish an infection (Brandenberger 2016; Simonetti 2014; Krone 2014).
Many infectious organisms can cause pneumonia, but the majority of community-acquired outpatient cases are attributable to the bacteria Streptococcus pneumoniae, Haemophilus influenzae, Legionella pneumophila, Staphylococcus aureus, and Mycoplasma pneumoniae and the influenza, parainfluenza, and respiratory syncytial viruses (Restrepo 2008; Marrie 2005; Cilloniz 2011; Torres 2013).
Pneumonia is categorized based on where it is contracted:
  • Community-acquired pneumonia is contracted outside of a hospital or other healthcare facility (ie, in the “community”), and often follows a viral respiratory infection such as a cold or the flu (Musher 2012; UMMC 2012). 
  • Hospital-acquired pneumonia is contracted during hospitalization. It tends to be more dangerous than community-acquired pneumonia because hospitalized patients generally have weakened immune systems and infectious bacteria found in hospitals have a greater tendency to be antibiotic resistant (UMMC 2012). Mechanical ventilation is a major risk factor for a type of hospital-acquired pneumonia called ventilator-associated pneumonia.
  • Healthcare-associated pneumonia affects patients in long-term healthcare facilities or those being treated in healthcare clinics such as kidney dialysis centers. As with hospital-acquired pneumonia, healthcare-associated pneumonia tends to be more serious and involve more dangerous pathogens than community-acquired pneumonia (Mayo Clinic 2015). Some doctors may use the term hospital-acquired pneumonia to encompass all pneumonia contracted via contact with any healthcare facility.

Risk Factors

A weakened immune response, such as caused by age-related immune senescence, immunosuppressive medications, or HIV infection, increases pneumonia risk (UMMC 2012; Murray 2015; Krone 2014). People over age 65 are at increased risk of pneumonia (Musher 2012; Mayo Clinic 2015; Loeb 2003). Other pneumonia risk factors include (Musher 2012; Torres 2013; Mayo Clinic 2015; UMMC 2012; Paju 2007; Sura 2012; Lambert 2015):
  • Smoking
  • Acute infections, such as colds or the flu (For more information on the treatment and prevention of colds and the flu, see the Common Cold and Influenza protocols.) 
  • Chronic diseases such as:
    • Chronic obstructive pulmonary disease (includes chronic bronchitis and emphysema) 
    • Asthma
    • Diabetes
    • Cardiovascular disease
    • Liver disease
    • Chronic kidney disease
    • Cancer
    • Periodontal disease 
    • Immune deficiency diseases
  • Drug or alcohol abuse
  • Neurological conditions that interrupt the gag reflex or impair swallowing, such as dementia and stroke 
  • Use of certain medications, including corticosteroids, immunosuppressants, and proton-pump inhibitors, and overuse of antibiotics resulting in antimicrobial resistance. Proton-pump inhibitors, which are normally used to suppress stomach acidity for relief of gastroesophageal reflux, may be a particularly problematic risk factor for pneumonia because their use is widespread and those who take them may be unaware that they are associated with significantly increased pneumonia risk.

4 Signs And Symptoms


Symptoms

The usual symptoms of pneumonia are (UMMC 2012; Torres 2013; Sethi 2014):
  • Fever and chills (though fever is often not present in older individuals) 
  • Chest or abdominal pain 
  • Pain with breathing (pleurisy)
  • Cough, dry or with phlegm; cough producing green or yellow sputum
  • Night sweats
  • Flu-like symptoms such as nausea, vomiting, muscle aches, fatigue, headache, and loss of appetite
  • Shortness of breath
  • Rapid heart and breathing rate
  • Weight loss
  • Nausea, vomiting, diarrhea
  • Confusion may occur among older individuals
Symptoms often come on rapidly and may be severe. However, older patients with a weakened immune response may not have the usual array of pneumonia symptoms, instead presenting with fatigue, disorientation, or confusion (Musher 2012).

Complications

In severe pneumonia, bacterial infection can spread to the surrounding lung tissue, causing an abscess. Pneumonia can also cause fluid accumulation between the pleura (membranes that surround the lungs), a condition known as pleural effusion. In empyema, the fluid between the pleura becomes infected, which can lead to permanent scarring (UMMC 2012).
Pneumonia-causing bacteria can enter the bloodstream (bacteremia) and spread infection to other parts of the body including joints, bones, muscle groups, heart valves, the abdominal cavity, and the meninges that surround the brain and spinal cord (Musher 2012).
Respiratory failure, including acute respiratory distress syndrome, is a dangerous complication in which the lungs are unable to function properly, resulting in life-threateningly-low blood oxygen concentrations (UMMC 2012).
Pneumonia is associated with kidney complications including end stage renal failure (Huang 2014), and studies have linked pneumonia to increased risk of arrhythmias, heart attack, and worsening of heart failure (Musher 2012; Aliberti 2014). Prolonged bed rest resulting from pneumonia can lead to blood clots (Torres 2013).

5 Diagnosis


Diagnosis of mild-to-moderate community-acquired pneumonia is typically based on medical history, physical exam, chest X-ray, and a complete blood count (Aoun 2016). Pulse oximetry, a noninvasive test that measures the oxygen level in the blood, can help assess pneumonia severity and whether hospitalization is needed (Torres 2013; Ortega 2011; Kaysin 2016). White blood cell numbers are generally elevated in people with pneumonia, but can also be low in some cases of overwhelming bacterial infection. CT scan may also be helpful in certain ambiguous cases (UMMC 2012; Musher 2012; Sethi 2014; Aoun 2016). Sputum gram stain and culture can help identify the presence and species of bacteria (UMMC 2012; Musher 2012). 
While identifying the infectious organism causing pneumonia can be helpful in choosing effective antibiotic treatment, physicians generally employ “empiric therapy” beginning immediately upon diagnosis of community-acquired pneumonia not requiring hospitalization (Cilloniz 2016). In empiric therapy, clinical judgment and knowledge of the patient and his or her condition guide treatment. This method is considered to have a high rate of success, and some authorities have recommended that attempts to identify the causative organism be reserved for more severe or problematic cases (Sethi 2014). 
In hospitalized patients, blood cultures can reveal widespread bacterial infection, usually from Streptococcus pneumoniae (Sethi 2014). Specific blood tests for atypical organisms are available (Cilloniz 2016). Urine antigen tests can detect the presence of proteins from Streptococcus pneumoniae and Legionella pneumophila more rapidly than cultures (Sinclair 2013; Molinos 2015; Aoun 2016). 
Invasive diagnostic procedures such as bronchoscopy or biopsy may be necessary in cases that do not respond to treatment as expected or in which unusual infectious organisms are suspected (Torres 2013).

6 Treatment


Antibiotics are the mainstay of bacterial pneumonia treatment. Guidelines for the management of community-acquired pneumonia published by the Infectious Diseases Society of America and the American Thoracic Society recommend initiating antibiotic therapy based on disease severity and the individual’s medical history rather than on microbial identification tests (Tedja 2013).
In previously healthy patients, usual first-line therapy includes antibiotics such as amoxicillin-clavulanic acid (Augmentin) or a macrolide antibiotic such as azithromycin, clarithromycin, or erythromycin. In patients with chronic health problems, recent antibiotic use, or other risk factors for drug-resistant bacterial infection, more aggressive treatment is preferred. These regimens are usually effective even when pneumonia is caused by infection with atypical bacteria such as Mycoplasma or Chlamydophila species (Simonetti 2014; Mandell 2007; Musher 2012).
All antibiotics, especially those with broad-spectrum activity, are associated with a range of possible side effects, from mild digestive upset to potentially life-threatening secondary intestinal infections such as Clostridium difficile colitis (Riddle 2009; Dallal 2002; Johanesen 2015).
Several analyses of trial data have found that adjunctive corticosteroids improve outcomes and reduce complication risk in community-acquired pneumonia. These benefits include a shorter length of hospital stay, reduced time to become clinically stable, reduced need for mechanical ventilation, and reduced risk of death in severe cases. These findings have led to recommendations that adjunctive corticosteroids be considered in hospitalized patients with severe community-acquired pneumonia if such treatment is not contraindicated (Siemieniuk 2015; Marti 2015; Horita 2015; Cilloniz 2016; Aoun 2016).
Viral pneumonia is often caused by influenza virus infection, though secondary bacterial pneumonia is a possible complication of viral pneumonia. Antiviral medications, including oseltamivir (Tamiflu) and zanamivir (Relenza), are sometimes used in these cases, though it is not certain that they can effectively treat established influenza virus pneumonia (Musher 2012; Chan 2016). Oseltamivir is associated with side effects including nausea and vomiting (Jefferson 2014).
In cases of severe pneumonia or in patients at high risk of complications, the physician may choose to recommend hospitalization so oxygen, ventilation assistance, and intravenous antibiotics and fluids can be provided (Black 1991; Fine 1990; Mandell 2007; Musher 2012).

Vaccination for Pneumonia Prevention

Vaccines targeting pneumococcal and influenza infections are the cornerstone of medical prevention of community-acquired pneumonia (Mandell 2007). Annual influenza vaccines reduce rates of influenza infections and influenza-associated pneumonia, as well as pneumonia complications and pneumonia hospitalizations (Grijalva 2015; Ridenhour 2013; Simpson 2013; Song 2015). The influenza vaccine is considered especially important for the elderly and other high-risk individuals (Song 2015).
Two pneumococcal vaccines, a 23-valent pneumococcal polysaccharide vaccine (Pneumovax®23) and a 13-valent pneumococcal conjugate vaccine (Prevnar13®) are available and generally recommended for people aged 65 and older and for all high-risk adults (NFID 2014; CDC 2016). The pneumococcal conjugate vaccine, in particular, is effective in eliciting an immune response in people with immune senescence (Kwetkat 2015; van Werkhoven 2015; de Roux 2008). A randomized controlled trial published in 2015, which enrolled nearly 85 000 volunteers aged 65 or older, found that PCV13 was effective in preventing community-acquired pneumonia and invasive pneumococcal disease caused by organisms against which the vaccine is designed to protect (Bonten 2015).
Pneumococcal vaccines also help combat antibiotic resistance, which can help reduce the prevalence of invasive disease caused by difficult-to-treat pneumococcal infections (Lipsitch 2016). Intriguingly, a meta-analysis found that use of the pneumococcal polysaccharide vaccine was associated with a significantly reduced risk of acute coronary syndrome in adults 65 and older (Ren 2015).

7 Novel And Emerging Strategies


Antimicrobial Stewardship

It is widely accepted that inappropriate and excessive antibiotic use has contributed to the emergence of increasing numbers of drug-resistant bacteria (Bosso 2011; Pinzone 2014; Roca 2015). Researchers in one extensive study found that approximately 25% of all Streptococcus pneumoniae samples were multidrug resistant, while another study found that more than 50% of Staphylococcus aureussamples isolated from patients with infections including pneumonia were multidrug resistant (Thornsberry 2008; Aliberti 2013). In regions with high antibiotic prescribing rates, resistant strains of Streptococcus pneumoniae are more common (Hicks 2011). The rising presence of resistant strains poses treatment challenges as well as public health dangers (Bosso 2011; Roca 2015).
The goal of antibiotic stewardship is to maximize beneficial clinical outcomes while minimizing negative and unintentional consequences of antimicrobial use. Adverse effects that judicious antimicrobial use may minimize include Clostridium difficile infections and multidrug-resistance (Dellit 2007; Barlam 2016).
A review of 14 scientific papers examining the application of the principles of antimicrobial stewardship in community-acquired pneumonia found an increase in appropriate antimicrobial use and a reduction in unnecessary antimicrobial prescribing. This was associated with better patient outcomes, including reduced 30-day and in-hospital mortality, shorter hospital stays, and reduced treatment failure rates and healthcare costs. A decrease in antimicrobial resistance was also observed (Bosso 2011).
Another strategy that is gaining attention is the use of shorter courses of some antibiotics in appropriate situations. Minimizing exposure to antibiotics may reduce the risk of inducing resistance (Rubinstein 2013). Short courses ranging from three to seven days have been found to be as effective for treating community-acquired pneumonia as a traditional 10-day course, but with lower risk of antibiotic-related adverse effects. This strategy also holds promise to decrease the risk of emergence of treatment-resistant organisms (Pinzone 2014).

Aspirin

Aspirin interacts with omega-3 fatty acid metabolic pathways to promote the formation of specialized inflammation-resolving molecules called “resolvins.” Resolvins and related molecules appear to be involved in the resolution of inflammatory conditions such as pneumonia (Serhan 2004; Oh 2011; Arita 2005). An animal model suggested that an aspirin-triggered resolvin exerts antibacterial activity in a model of pneumonia and could complement antibiotic therapy (Abdulnour 2016). A study on 1005 pneumonia patients admitted to a hospital in Italy with community-acquired pneumonia showed that those who were chronic aspirin users were about half as likely to die within 30 days of hospital admission as those not taking aspirin (Falcone 2015). 
One serious complication of severe pneumonia is acute coronary syndrome, which occurs when the heart does not get enough blood flow (AHA 2015). One randomized open-label study enrolled 185 pneumonia patients upon hospital admission. Ninety-one of the participants received aspirin, while 94 served as a control group. The rate of acute coronary syndrome in the control group during the 30 days following admission was 10.6%, while the corresponding rate in the aspirin-treated group was only 1.1%. In addition, the aspirin recipients were significantly less likely to die from cardiovascular causes (Oz 2013).

Statins

In keeping with the goal of reducing antibiotic use, non-antibiotic treatments for pneumonia are an area of active investigation. The use of statins, a class of cholesterol-lowering medication, has been associated with decreased risk of pneumonia and pneumonia-related death, as well as reduced rates of acute bacterial infections (Nassaji 2015; Lin, Chang 2016; Cheng 2014; Terblanche 2007). Statins appear to inhibit lung inflammation through modulation of neutrophil activity, inhibition of inflammatory cytokines such as nuclear factor-kappa B, and induction of an enzyme that limits oxidative stress. One study evaluated the association between statin use and efferocytosis, an inflammation-resolving process involved in recovery from pneumonia, in 22 community-acquired pneumonia patients in London. This study found that statin use was associated with higher rates of efferocytosis, an effect that was most prominent in smokers (Wootton 2016). Also, community-acquired pneumonia is associated with an increased risk of cardiovascular events, and individuals taking statins may have some protection from this risk. Further studies will be required to clarify the potential role of statins in preventing and treating pneumonia and its complications (Troeman 2013; Feldman 2015). 

Blood Procalcitonin Testing to Guide Antibiotic Therapy

Elevated blood levels of a protein called procalcitonin are suggestive of a bacterial infection (Musher 2012). Along with consideration of the patient’s clinical status, measuring procalcitonin levels may help guide antibiotic therapy decisions in patients with community-acquired pneumonia (Pinzone 2014; Montassier 2013). One analysis suggested that using procalcitonin testing to determine if antibiotics should be administered reduced total antibiotic exposure and duration of antibiotic treatment (Christ-Crain 2006). Another analysis showed that procalcitonin-guided antibiotic prescribing to patients with respiratory infections, including pneumonia, reduced the median duration of antibiotic exposure by half (Schuetz 2012).

8 Diet And Lifestyle Considerations


Many cases of community-acquired pneumonia begin with a simple cold or a flu (van der Sluijs 2010; Lee 2010; NLM 2016a). Thus, one of the most important ways to avoid pneumonia is to maintain good overall health and keep the immune system functioning normally (Musher 2012; Craig 2009; NLM 2016b; ALA 2016). For more information on ways to avoid the cold and flu, see Life Extension’s Common Cold and Influenza protocols.
  • Avoid smoking and excessive alcohol consumption. Smoking is the most important risk factor for community-acquired pneumonia that is under an individual’s control. Also, excessive alcohol consumption increases the risk of community-acquired pneumonia (Almirall 2015).
  • Healthy diet. Nutrient deficiencies and malnutrition are common in older people and contribute to pneumonia risk (Ahmed 2010; Evans 2005; Gaillat 2003), but may be preventable through a well-rounded nutrient-dense diet and dietary supplementation (Stechmiller 2003; Park 2008; Guyonnet 2015).
  • Exercise. Substantial evidence indicates engaging in regular physical activity diminishes some of the negative effects of aging on immune cell activity (Senchina 2007) and physically active seniors have fewer infections than their sedentary counterparts (Simpson 2010). Exercise is thought to exert these benefits by activating immune cells, helping expel bacteria from the airways, and reducing stress (NLM 2014).
  • Basic hygiene. Regular hand washing is recommended as a strategy for avoiding respiratory infections (UMMC 2012). Regular water or saline nasal irrigation may also help keep respiratory infections at bay (AFP 2009).
Once pneumonia has set in, adequate water intake is especially important for keeping the mucus in the lungs loose. In addition, getting plenty of rest until symptoms are completely resolved may help prevent recurrence (Mayo Clinic 2015).

Poor Oral Health Increases Pneumonia Risk

Because harmful bacteria in the mouth can be aspirated into the lungs and cause infection (Barnes 2014), poor oral hygiene is associated with a higher risk of pneumonia (Torres, Peetermans 2013; Raghavendran 2007; El Attar 2010).
One study that assessed the rate of respiratory illness among a group of older adults demonstrated the importance of thorough oral hygiene. During a six-month period, only 1 of 98 aging adults who utilized dental hygienists for oral health care developed respiratory infections, compared with 9 of 92 people who did not receive the same preventative dental care (Adachi 2007).
In addition, a daily water gargling habit has been found to reduce the incidence of upper respiratory tract infections, perhaps by keeping infectious microbes from sticking to the oral surfaces (Satomura 2005). Gargling with salt water may also prevent respiratory tract infections, which often precede pneumonia (Emamian 2013).
Several strategies for maintaining good oral health are described in Life Extension’s Oral Health protocol.

9 Integrative Interventions


Note: In addition to reviewing the integrative interventions described here, readers are encouraged to review those described in the Immune Senescence protocol. Immune senescence is an important risk factor for pneumonia, and, therefore, natural compounds shown to combat immune senescence may help reduce pneumonia risk. Similarly, because colds and the flu are risk factors for pneumonia, the Common Coldand Influenza protocols should be consulted as well.

Probiotics

When hospitalized patients require assisted ventilation for 48 hours or more, their risk of developing hospital-acquired pneumonia increases (Liu 2012). Meta-analyses of randomized controlled trial data have concluded that probiotics may prevent hospital-acquired pneumonia in critically ill patients (Liu 2012; Barraud 2013; Petrof 2012; Bo 2014) and lessen the incidence and duration of upper respiratory tract infections in healthy adults and children (Hao 2015; King 2014; Saeterdal 2012). A double-blind placebo-controlled clinical trial on more than 200 healthy subjects tested whether probiotic formulas impacted the rate and severity of respiratory illness over three winters. The trial used formulas containing multiple strains of Lactobacilli (including Lactobacillus plantarum LP 02-LMG P-21020), as well as Bifidobacterium lactis BS 01-LMG P-21384. The frequency, severity, and duration of respiratory illnesses during cold and flu season were significantly reduced in the probiotic group compared with the placebo group (Pregliasco 2008). Since many cases of bacterial pneumonia are preceded by upper respiratory tract infections (Musher 2012), preventing these milder infections may reduce pneumonia risk. Probiotics are also useful in minimizing side effects of antibiotic therapy, including diarrhea and Clostridium difficile infection (Urben 2014; Maziade 2015).  

Reishi

Ganoderma lucidum, commonly known as reishi or lingzhi, has a long history of use for treating conditions related to inflammation and low immune function (Suarez-Arroyo 2013; Wachtel-Galor 2011; Patel 2012; Batra 2013). Because of its balancing effect on immune activity, reishi is considered an immune modulator (Bhardwaj 2014). Reishi polysaccharides have been found to stimulate infection-fighting immune cells (Tsai 2012; Zhu 2005). 

Cistanche

Cistanche deserticola has been used historically in traditional Chinese medicine to stimulate immunity in the elderly. Cistanche glycosides, including the compound echinacoside, as well as a cistanche polysaccharide have demonstrated immune-enhancing effects (Xuan 2008; Wu 2005; He 2009). An extract of cistanche was found to increase lifespan and stimulate immune cell activity in mice with immune senescence. Because immune senescence plays a key role in pneumonia susceptibility in older individuals (Krone 2014; McElhaney 2012; Murray 2015; Zhang 2014), cistanche holds promise as a pneumonia preventive in the elderly. 

Pu-erh Tea

Pu-erh tea has been used traditionally in China for centuries for a wide range of health benefits. Pu-erh tea was found to enhance immune cell activity while decreasing the inflammatory cytokine interleukin-6 in mice with immune senescence (Zhang 2012). This immune-modulatory effect gives pu-erh tea potential as a pneumonia preventive in aging individuals. 

Vitamin D

Data from the National Health and Nutrition Examination Survey III showed occurrence of community-acquired pneumonia was higher in people with low vitamin D status (Quraishi 2013). In another study that followed over 1400 people between the ages of 53 and 73 for an average of almost 10 years, those with the lowest vitamin D levels were 2.6 times more likely to develop pneumonia compared with those with the highest vitamin D levels (Aregbesola 2013). Very low (< 15 ng/mL) 25-hydroxyvitamin D levels have been associated with 2.6-fold greater odds of hospitalization for community-acquired pneumonia (Jovanovich 2014). Furthermore, vitamin D deficiency may increase the risk of death in hospitalized patients with community-acquired pneumonia (Kim 2015; Leow 2011). An ongoing randomized, placebo-controlled, double-blind clinical trial, called the Lung VITAL study, is examining whether supplementing with 2000 IU vitamin D plus 1 g omega-3 fatty acids from fish per day can reduce pneumonia risk (Gold 2016). An analysis of randomized controlled trial data found vitamin D supplementation reduced the odds of respiratory infections by over 40% (Charan 2012). 
These benefits may be partly explained by vitamin D’s ability to increase antimicrobial immune activity (Borella 2014; Youssef 2012). Also, vitamin D deficiency is associated with fewer immune cells in the blood, increasing susceptibility to infection (Dogan 2009; Youssef 2012). Vitamin D is also an immune modulator, involved in stimulating innate immune activity and regulating tissue-damaging inflammation (Youssef 2012; Lin 2016; Calton 2015). 

Zinc

Poor zinc status, a common finding in the elderly, is associated with impaired immune function, decreased defenses against microbes, increased duration and incidence of pneumonia, and greater use of antimicrobial treatments. Low zinc levels are also associated with an increased rate of death from all causes in the elderly. Because zinc is needed for normal cell division and development, it is especially important to cells that replicate rapidly, such as immune cells (Barnett 2010).  
In a one-year study, nursing home residents with lower zinc status were found to have almost twice the risk of pneumonia as those with normal zinc status. In addition, pneumonia lasted longer and more antibiotics were used in the low-zinc residents compared with their normal-zinc counterparts. Study subjects with adequate zinc levels were at a significantly lower risk of dying from any cause (Meydani 2007). In an animal model, mice fed a zinc-deficient diet were dramatically more likely to die of infection with Streptococcus pneumoniae, and to have evidence of lung infection with Streptococcus pneumoniae, compared with mice fed zinc-adequate diets (Strand 2001).
Zinc supplements may reduce the duration and severity of upper respiratory tract infections. In one trial, volunteers with recent onset of cold symptoms were treated with 13.3 mg zinc, in the form of an oral zinc acetate lozenge, or placebo every 2–3 hours during the day. Zinc-treated subjects had less severe symptoms and recovered an average of 3.1 days sooner than placebo-treated subjects (Prasad 2008). In a similar trial, taking a lozenge providing 12.8 mg zinc acetate every 2–3 hours, beginning within 24 hours of developing a cold, was associated with decreased severity of symptoms and a 3.6-day reduction in duration of symptoms (Prasad 2000). Zinc may also be useful in prevention. A randomized controlled clinical trial in adults aged 55–87 found daily supplementation with 45 mg zinc gluconate for 12 months was associated with lower incidence of infections compared with placebo (Prasad 2007). Since pneumonia is often a complication of an upper respiratory tract infection (Musher 2012), preventing colds or reducing their severity may help protect against pneumonia. 

Vitamin E

In a one-year controlled clinical trial, over 600 elderly nursing home residents were treated daily with 200 IU vitamin E or placebo. Those receiving vitamin E experienced fewer common colds (Meydani 2004). Another study following elderly patients hospitalized with community-acquired pneumonia found taking vitamin E supplements was associated with 63% lower odds of re-hospitalization after discharge (Neupane 2010). Based on work in animal models of susceptibility to infection in the elderly, vitamin E appears to exert its protective effect against bacterial pneumonia through modulation of immune function (Bou Ghanem 2015). 
Vitamin E is not a single compound, but rather comprises several related compounds called isoforms (Abdala-Valencia 2013). A combination of natural tocopherols may possess greater health-promoting properties compared with isolated alpha-tocopherol. Gamma-tocopherol in particular seems to be an important contributor to some of vitamin E’s health benefits (Peh 2016; Mathur 2015; Devaraj 2008; Lee 2009; Wu 2007). 

Green Tea

Green tea is rich in polyphenolic compounds called catechins (Taylor 2005). A major catechin in green tea, epigallocatechin gallate or EGCG, has demonstrated antiviral action against influenza virus (Ling 2012) and has been shown to activate antibacterial immunity against Legionella pneumophila in vitro (Matsunaga 2002; Yamamoto 2004). Green tea catechins have demonstrated important antimicrobial activity against oral pathogens that cause periodontal disease, which may be a risk factor for development of bacterial pneumonia (Taylor 2005; Raghavendran 2007).
A study that followed older subjects for 12 years found that women who drank one or more cups (averaging about 3.5 fl oz per cup) of green tea per day were 41–47% less likely to die from pneumonia than women who drank less than one cup of green tea per day (Watanabe 2009). Drinking 1–5 cups of green tea daily was found in another study to reduce the risk of influenza, a common prelude to pneumonia, in schoolchildren (Park 2011; Chan 2016).
In a controlled clinical trial in nearly 200 healthcare workers, a green tea extract providing 378 mg per day of green tea catechins and 210 mg per day of the green tea-derived amino acid theanine was compared with placebo. Subjects in the green tea extract group had 75% fewer influenza infections over a five-month period (Matsumoto 2011). Gargling with a catechin-rich green tea extract may also be an effective way to prevent respiratory infections, including influenza. In a 3-month study, 148 nursing home residents were assigned to gargle regularly with either a solution containing green tea catechins or a catechin-free control solution. Only 1.3% of residents in the catechin group contracted influenza, while 10% of those in the control group became ill with the flu (Yamada 2006).

N-acetylcysteine and L-cystine

N-acetylcysteine (NAC) is a precursor to glutathione, one of the body’s essential oxidative stress modulators, and has been studied in bronchitis, cystic fibrosis, and other lung conditions because of its expectorant and mucus-thinning actions (van Zandwijk 1995; Tirouvanziam 2006; Roxas 2007; Chen 2013). NAC supplementation increases the body’s stores of glutathione, and evidence indicates that NAC improves immunity and modulates inflammation (McCarty 2015). In a six-month trial with 262 participants, most of whom were 65 or older, only 25% of those taking 600 mg NAC twice daily developed influenza symptoms compared with 79% of those in the placebo group. NAC treatment significantly decreased the severity and frequency of influenza-like episodes, and reduced time spent recovering in bed (De Flora 1997). Influenza often precedes community-acquired pneumonia (Musher 2012), suggesting that NAC might offer some protection against pneumonia in older adults. 
A combination of L-cystine and another amino acid, L-theanine (found in green tea), may also protect against viral infections that could lead to pneumonia (Jain 2016; Soboleva 2004; Boros 2016). Taken daily for 14 days prior to vaccination, 700 mg L-cystine plus 280 mg L-theanine improved immune response to the influenza vaccine to a greater degree than placebo in nursing home residents (Miyagawa 2008). In another trial, healthy men taking 350 mg L-cystine plus 140 mg L-theanine twice daily had 58% fewer colds in a 35-day period than those taking placebo (Kurihara 2010).

Echinacea

Echinacea is an immunomodulator that can stimulate antimicrobial immune function but inhibit overly inflammatory immune activity (Zhai 2007; Goel 2005). A rigorous analysis of randomized controlled trials of echinacea preparations concluded that echinacea use can prevent repeated respiratory infections and their complications, including pneumonia. The analysis also determined that using higher doses of echinacea during infections improved its efficacy (Schapowal 2015). 
Preliminary research suggests early treatment of cold symptoms with echinacea may speed recovery (Lindenmuth 2000; Goel 2005). Early treatment of influenza with an echinacea preparation was found to be as effective as the antiviral medication oseltamivir (Raus 2015).
Individuals at high risk of pneumonia due to chronic respiratory conditions may benefit from the use of echinacea. In a pilot trial, adults with pre-existing chronic respiratory conditions were treated with either influenza vaccine, a standardized echinacea extract, or both. Those treated with the echinacea extract, with and without the flu shot, experienced fewer flu-like symptoms and had fewer respiratory complications during the study period compared with those who received only the vaccine (Di Pierro 2012). 

Vitamin C

Some trials have found a benefit of vitamin C supplementation in the prevention of pneumonia, and a review of trials of vitamin C for the common cold found a reduction in severity and duration of colds (Hemila, Chalker 2013; Hemila, Louhiala 2013). Serum levels of vitamin C have been found to be lower in patients with pneumonia than in healthy people (Bakaev 2004). Even a modest dose of 200 mg per day has been shown to raise serum levels and improve the symptomatic condition of individuals with acute respiratory infections (Hunt 1994). Vitamin C has been shown to reduce oxidative stress and levels of inflammatory biomarkers in a preclinical model of severe community-acquired pneumonia (Chen 2014).

Garlic

In a controlled clinical trial lasting 12 weeks during winter, volunteers taking a garlic supplement had fewer and shorter colds than volunteers taking a placebo (Josling 2001). In another randomized controlled trial, healthy subjects taking an aged garlic extract reported fewer and less severe cold and flu symptoms, and less school and work days missed, during the 3-month study period compared with placebo. Furthermore, blood tests after 45 days showed superior immune cell proliferation in the garlic extract group compared with placebo (Nantz 2012). In a preclinical study, garlic extract demonstrated antibacterial action against both Streptococcus pneumoniae and a less common cause of pneumonia, Klebsiella pneumoniae (Dikasso 2002). A randomized controlled trial published in 2016 investigated the effect of aged garlic extract supplementation on the incidence and severity of colds and the flu. Participants (n=120) were randomized to receive aged garlic extract (2.56 g daily) or placebo for 90 days during cold and flu season. After 45 days, specialized cytotoxic T cells called gamma-delta T cells and NK cells from the garlic recipients proliferated better and were more activated than those from placebo recipients. After 90 days, those who received aged garlic extract reported reduced cold and flu severity, fewer symptoms, and less absenteeism from work and school (Percival 2016).

rif. Dr. Silvia Furiani:>>

Coenzyme Q10

Coenzyme Q10 (CoQ10) is found in all metabolically active cells of the body. Supplemental CoQ10 may benefit people with pneumonia by inhibiting inflammation, improving cellular energy metabolism, and modulating oxidative stress. In one randomized controlled clinical trial, older adults hospitalized with community-acquired pneumonia were given either 200 mg CoQ10 daily or placebo, in addition to antibiotics, for 14 days. At the end of the trial, it was noted that fevers had resolved more quickly, hospital stays were shorter, recovery rates were higher, and treatment failure rates were lower in the CoQ10 group compared with the placebo group (Farazi 2014). 

rif. Dr. Silvia Furiani:>>

Disclaimer and Safety Information

This information (and any accompanying material) is not intended to replace the attention or advice of a physician or other qualified health care professional. Anyone who wishes to embark on any dietary, drug, exercise, or other lifestyle change intended to prevent or treat a specific disease or condition should first consult with and seek clearance from a physician or other qualified health care professional. Pregnant women in particular should seek the advice of a physician before using any protocol listed on this website. The protocols described on this website are for adults only, unless otherwise specified. Product labels may contain important safety information and the most recent product information provided by the product manufacturers should be carefully reviewed prior to use to verify the dose, administration, and contraindications. National, state, and local laws may vary regarding the use and application of many of the therapies discussed. The reader assumes the risk of any injuries. The authors and publishers, their affiliates and assigns are not liable for any injury and/or damage to persons arising from this protocol and expressly disclaim responsibility for any adverse effects resulting from the use of the information contained herein.
The protocols raise many issues that are subject to change as new data emerge. None of our suggested protocol regimens can guarantee health benefits. Life Extension has not performed independent verification of the data contained in the referenced materials, and expressly disclaims responsibility for any error in the literature.

PUBLIC LAW 109–417—DEC. 19, 2006 - LEGGE US SU VACCINI DEL 2006


SEC. 319A. VACCINE TRACKING AND DISTRIBUTION.
‘‘(a) TRACKING.—The Secretary, together with relevant manu- facturers, wholesalers, and distributors as may agree to cooperate, may track the initial distribution of federally purchased influenza vaccine in an influenza pandemic. Such tracking information shall be used to inform Federal, State, local, and tribal decision makers during an influenza pandemic.
FONTE: web cercare:
" PLAW-109publ417.pdf "

CERCASI RICERCATORI COVID 19

FONTE RESEARCH GATE sito: https://www.researchgate.net/scientific-recruitment/blog/post/covid-19-free-job-posts-and-job-ads-for-teams-tackling-coronavirus

COVID-19: Free job posts for teams tackling coronavirus

As the global number of confirmed cases of COVID-19 continues to rise, ResearchGate is opening up its scientific job board and allowing teams actively working to combat the pandemic to post job advertisements for free.

Any team — whether part of an academic institution, company, research lab, hospital, society, or NGO — that needs to recruit scientists, researchers, or scientific support staff to combat the pandemic may now qualify to post advertisements for these roles on our network free of charge (for a limited time).


A FUTURA MEMORIA

Tratto dall'editoriale del presidente dell'Ordine dei Medici di Milano sito  https://www.omceomi.it/medici del  marzo 2020

SUI MEDICI

A futura memoria “Écoutant, en effet, les cris d’allégresse qui montaient de la ville, Rieux se souvenait que cette allégresse était toujours menacée. Car il savait ce que cette foule en joie ignorait, et qu’on peut lire dans les livres, que le bacille de la peste ne meurt ni ne disparaît jamais, qu’il peut rester pendant des dizaines d’années endormi dans les meubles et le linge, qu’il attend patiemment dans les chambres, les caves, les malles, les mouchoirs et les paperasses, et que, peutêtre, le jour viendrait où, pour le malheur et l’enseignement des hommes, la peste réveillerait ses rats et les enverrait mourir dans une cité heureuse.” “Ascoltando, infatti, le grida d’allegria che salivano dalla città, Rieux ricordava che quell’allegria era sempre minacciata: lui sapeva quello che ignorava la folla, e che si può leggere nei libri, ossia che il bacillo della peste non muore né scompare mai, che può restare per decine di anni addormentato nei mobili e nella biancheria, che aspetta pazientemente nelle camere, nelle cantine, nelle valigie, nei fazzoletti e nelle cartacce e che forse verrebbe giorno in cui, per sventura e insegnamento agli uomini, la peste avrebbe svegliato i suoi topi per mandarli a morire in una città felice.” ALBERT CAMUS, La peste 4 INFORMAMI EDITORIALE ospedali. I medici di medicina generale della zona rossa (cioè dei paesi del lodigiano) ne hanno ricevuti in piccola quantità. Nulla è arrivato ai medici di medicina generale del resto della ATS Milano (e in diverse parti della Lombardia)! Non solo: i ricoverati aumentano e si intravede un problema anche e soprattutto nelle terapie intensive, i cui posti letto possono diventare rapidamente insufficienti, nel giro di pochi giorni o di poche ore. Domenica 23 ho contattato un funzionario regionale: alle mie rimostranze, mi spiegava che avevano pensato a contenere l’emergenza nel lodigiano e poi, da lunedì, avrebbero anche pensato ai medici del territorio!… A questo punto, direi che è già il caso di fare un primo parziale bilancio di ciò che è accaduto, soprattutto nella prospettiva di interventi futuri. Abbiamo visto e avuto conferma che le istituzioni politiche e amministrative sono abituate a non tenere in gran conto i medici e gli operatori sanitari. Nell’ordinaria amministrazione, un medico che va a casa di un paziente ammalato è considerato come un artigiano che deve riparare qualcosa che si è rotto in casa. Mica ha bisogno del contrassegno! Nell’emergenza, le decisioni non sembra vengano prese alla luce di ragionamenti di ordine scientifico, ma politico, e i medici e gli odontoiatri, semplicemente, non vengono considerati come coloro che sono in prima linea. Ci si ricorda, stancamente, che bisogna proteggerli solo quando questi si lamentano di essere lasciati da soli. La mancanza di coordinamento tra e nelle istituzioni è evidente e i messaggi che vengono inviati sono contraddittori e spesso contrastanti. Non solo, la mancanza di preparazione lascia sconcertati, poiché il mondo occidentale e il nostro Paese non sono nuovi a emergenze simili. Certo, SARS1 e MERS, per fortuna, non sono “esplose” in Occidente, ma il pericolo era evidente. Ebbene, l’incertezza può essere scusabile nelle prime ore della diffusione del contagio, ma non dopo una settimana! In sintesi: nell’immediato, vanno subito protetti adeguatamente gli operatori sanitari e va subito messo in atto un piano per fronteggiare il probabile aumento dei ricoveri, e da subito bisogna pensare a potenziare i posti letto delle terapie intensive, visto che, nel frattempo, le malattie ordinarie non vanno in vacanza. Le comunicazioni devono essere chiare e univoche e vanno sempre supportate dal fondato e concorde parere degli esperti. I brutti momenti che i medici stanno vivendo passeranno, ci si augura. La SARS-CoV2 diventerà un ricordo. Per il futuro, tuttavia, un Paese come il nostro e una Regione come quella in cui viviamo, non potranno non dotarsi di un piano di emergenza che permetta, in tempi molto rapidi, di porre in essere tutte le misure necessarie al diffondersi di un’altra epidemia. Da ultimo, fatemelo dire per l’ennesima volta: basta precari nei reparti ospedalieri e tra i ricercatori! Dotiamoci di un numero adeguato di medici di ruolo in forza agli ospedali pubblici e privati e di ricercatori che ci possano supportare nell’ordinaria e nella straordinaria amministrazione.

KLEBSIELLA: CRESCE LA POLMONITE OSPEDALIERA

Klebsiella, cresce la polmonite ospedaliera

Di Ermanno Faccio

tratto dal web

Come si contraggono le infezioni da Klebsiella?

In anni recenti l’infezione da Klebsiella si è particolarmente diffusa negli ambienti ospedalieri; le klebsielle sono però presenti un po’ ovunque. Possono colonizzare la pelle, la faringe e il tubo digerente, le ferite e le urine, e possono essere trasmesse mediante contatto della pelle con superfici contaminate, attraverso le feci, per via aerea e, in alcuni casi, per via sessuale o da madre a figlio.

Sintomi e malattie associate alle infezioni da Klebsiella

Le infezioni da Klebsiella sono associate principalmente a:
  • polmoniti contratte in ambiente ospedaliero
  • infezioni delle vie urinarie
  • infezioni nosocomiali
  • rinoscleroma
  • ozena
  • ulcere genitali croniche

A seconda dei casi i sintomi dell’infezione possono includere:
  • febbre
  • brividi
  • manifestazioni simil influenzali
  • tosse con espettorato denso, a volte contenente sangue
  • aumento della minzione
  • urgenza nella minzione
  • fastidio alla parte alta del pube
  • dolori alla parte bassa della schiena
  • presenza di batteri nelle urine
  • papule o noduli a livello dei genitali

Che cosa sono le infezioni da Klebsiella?

Con il termine Klebsiella si indica un genere di batteri appartenenti alla famiglia delle Enterobacteriaceae. Si tratta di bastoncelli Gram-negativi dotati di una notevole capsula polisaccaridica che forniscono loro una altrettanto notevole resistenza alle difese dell’organismo che infettano.
Le specie di Klebsiella associate a malattie che colpiscono l’uomo sono 3: 
  • K. pneumoniae (con le sottospecie K. ozaenae e K. rhinoscleromatis)
  • K. Oxytoca
  • K. granulomatis

Cure e trattamenti

Il trattamento più adatto in caso di infezione da Klebsiella dipende dagli organi coinvolti. In genere all’inizio si procede empiricamente tentando la strada del trattamento con antibiotici, ad esempio con cefalosporine di terza generazione, carbapenemi, aminoglicosidi o chinoloni, a volte consigliati in combinazioni. A volte anche ceftazidima, cefepime, levofloxacina, norfloxacina, moxifloxacina, meropenem, ertapenem e le combinazioni ampicillina/sulbactam, piperacillina/tazobactam e ticarcillina/acido clavulanico risultano efficaci.
Purtroppo, però, le klebsielle sono spesso resistenti a più antibiotici: gli enzimi carbapenemasi prodotti da K. pneumoniae sono associati a una mortalità superiore al 50%. 
A volte possono essere necessari trattamenti chirurgici, ad esempio per drenare ascessi polmonari.



Con il termine Klebsiella si indica un genere di batteri appartenenti alla famiglia delle Enterobacteriaceae. Si tratta di bastoncelli Gram-negativi dotati di una notevole capsula polisaccaridica che forniscono loro una altrettanto notevole resistenza alle difese dell’organismo che infettano.
Le specie di Klebsiella associate a malattie che colpiscono l’uomo sono 3: 
  • K. pneumoniae (con le sottospecie K. ozaenae e K. rhinoscleromatis)
  • K. Oxytoca
  • K. granulomatis

Cure e trattamenti

Il trattamento più adatto in caso di infezione da Klebsiella dipende dagli organi coinvolti. In genere all’inizio si procede empiricamente tentando la strada del trattamento con antibiotici, ad esempio con cefalosporine di terza generazione, carbapenemi, aminoglicosidi o chinoloni, a volte consigliati in combinazioni. A volte anche ceftazidima, cefepime, levofloxacina, norfloxacina, moxifloxacina, meropenem, ertapenem e le combinazioni ampicillina/sulbactam, piperacillina/tazobactam e ticarcillina/acido clavulanico risultano efficaci.  



Disclaimer
Le informazioni riportate rappresentano indicazioni generali e non sostituiscono in alcun modo il parere del medico. In caso di malessere è consigliabile rivolgersi al proprio medico o recarsi al pronto soccorso.

MARA VENIER: DOVETE RESTARE A CASA, LO DICONO TUTTI

CODICE MEDICO, SW ASSISTANTRL, (CODICE CALE), COGNOME, NOME, ENTE DI APPARTENENZA, SEDE ATTIVITA', PRESTAZIONE, CA SPECIALITA', CODICE SPECIALITA' (CREDENZIALE ESTESA), CENTRI DI PRESCRIZIONE LRCSRN71E55C342Y ALERCI SERENA AIAS di P. Mantegazza, ICA BRLSBN71T43L682O BARATELLI SABINA AIAS di P. Mantegazza, NEUROPSIATR IA INFANTILE NEUP CSTDNL72T56F205C COSTANZO DANIELA MARIA AIAS di P. Mantegazza, NEUROPSIATR IA INFANTILE NEUP NGLRRT57L04F205A ANGELINI ROBERTO ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio ICA PDA D'ARTO INFERIORE RSAMRG55T11I690P AROSIO AMBROGIO ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio ICA BGNRRT56R18F205K BAGNOLI ROBERTO ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio GERIATRIA GER BRBLSN52L27G912U BARBARELLI ALESSANDRO ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio BRFSNO63S52L392Y BARUFFI SONIA ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 1 di 117
2 CLCFNC57P51F205C CALASSO FRANCESCA ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio GERIATRIA GER CRDLLD69P44Z504E CARDOSO OLGA LIDIA ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio ICA PDA D'ARTO INFERIORE CRTRNN57D17F205Y CAROTENUTO ERMANNO ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio MALATTIE DELL'APPARATO RESVMD CTRSHN71E55F205S CATARAME SARAH ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio CLMSNN56T44D969A CLEMENTI SUSANNA ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio ICA CLLGDU59A20F205Y COLLODO GUIDO ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio e cura DLCPLA52E18F029L DE LUCA PAOLO ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio GERIATRIA GER DSTDLV62M52C351W DI STEFANO DANIELA VERA ANTONIETTA ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio ICA NGDLRI73D56F205A ENGADDI ILARIA ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio GERIATRIA GER GLLGRG56M11F205H GALLIMBENI GIORGIO ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio MALATTIE DELL'APPARATO RESVMD ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 2 di 117
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4 RSSPLG55P23F205M ROSSI PIERLUIGI ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio ICA PDA D'ARTO INFERIORE SCPFNC57E21F205U SCAPELLATO FRANCO ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio GERIATRIA GER TRTMRC51B20F205D TURATI MARCO ASP Istituti Milanesi Martinitt e Stelline e PAT A.T. Trivulzio ICA BRTLRN65L54F205U BERTONI LORENA ASP Istituto Golgi Redaelli Bartolomeo D'Alviano, GERIATRIA GER CSTRCR60T06F205N CASTOLDI RICCARDO ASP Istituto Golgi Redaelli Bartolomeo D'Alviano, GERIATRIA GER DNGRRT50E06F205J D'ANGELO ROBERTO ASP Istituto Golgi Redaelli Bartolomeo D'Alviano, GERIATRIA GER FBBSFN62T19A390Y FABBRINI STEFANO ASP Istituto Golgi Redaelli Bartolomeo D'Alviano, ICA FGTLNE64R62F205Z FOGATO ELENA ASP Istituto Golgi Redaelli Bartolomeo D'Alviano, GERIATRIA GER GNDMCR65S67F205R GANDOLFI MARIA CARLA ASP Istituto Golgi Redaelli Bartolomeo D'Alviano, GERIATRIA GER GRLNNS56M27F205K GRILLO ANTONIO ASP Istituto Golgi Redaelli Bartolomeo D'Alviano, GERIATRIA GER ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 4 di 117
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7 FCCRTM46D23C728E FRCGNN63R64I976K GMBNNA79H58I628P FACNI RENATO FORACA GIOVANNA GAMBARARA ANNA GRMMRN56M56F205H GERMANI MARINA NCRCST51B06L331J LZJMLE50M63C933R MNTGLG50M15F205Z MGLRFL58T81F205D MTVKRS57M24Z224R PRNLRT57T29F205C INCORVAIA CRISTOFORO LOZEJ EMILIA MANTOVANI GIANLUIGI MEGALI RAFFAELLA MOTAVALLI KOUROS PARONZINI ALBERTO CTO) CTO) CTO) CTO) CTO) CTO) CTO) CTO) CTO) CTO) Bignami, Bignami, Bignami, Bignami, Bignami, Bignami, Bignami, Bignami, Bignami, Bignami, ICA ICA MALATTIE DELL'APPARATO RESVMD ICA ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 7 di 117
8 PCCDNC69C05F704E PRVCHR74P69F205K RRSGGL57P28G702L SCLGRG62D25F205W SNTFNC59P10F704U SCZNNL58M53F205Z SCHSDR54L09Z336J TGLLDM54A69B300E VGNCDR63D10F205I ZCCNLN56E69F205I PICCININI DOMENICO PRAVETTONI ARA RIARIO SFORZA GIAN GALEAZZO SACILOTTO GIORGIO SANTAMARIA FRANCESCO SCAZZOSO ANTONELLA SLTON ISIDORO TAGLIORETTI JOLANDA VIGNATI CLAUDIO ZECNELLI ANNA LENA CTO) CTO) CTO) CTO) CTO) CTO) CTO) CTO) CTO) CTO) Bignami, Bignami, Bignami, Bignami, Bignami, Bignami, Bignami, Bignami, Bignami, Bignami, MALATTIE DELL'APPARATO MALATTIE DELL'APPARATO RESVMD RESVMD ICA ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 8 di 117
9 ZNNRNG61A57F704N ZENNATO ROSANGELA BRTMSM54M24F205G BARATELLI MASSIMO BRNGPP52C2F205F BERNABE' GIUSEPPE BRRMSM59R29L219W BERRUTO MASSIMO BNFDNL53L03F704O BRSCLD57H30F205Y BTTPFL57A03F205T BRMSRG53E29F205I BCCMLS57C09Z614H CSRNNL61B08H224D BONFANTI DANIELE BORSOTTI CLAUDIO BOTTIGLI AMICI PIERFILIPPO BRAMBILLA SERGIO BUCCI MIGUEL CASERTA ANTONELLO CTO) Bignami, ICA Isocrate PDA D'ARTO INFERIORE ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 9 di 117
10 CFLVTR60A10F132T CRRCTN66R20F205K CSTRSL79A51H357P CSTVLR81H55F839A CRTFBA55L19C669Z DLAPRM54R09B910U DBLMRT67P25M052K DLLNDR84P29C573H DLCGRL61M07E691X DCUDRA55H15E704L CEFALO VITTORIO CORRADINI COSTANTINO COSTANTINO ROSSELLA COSTANTINO VALERIA CURTI FABIO DAOLIO PRIMO ANDREA DE BELLIS UMBERTO DELLA VALLE ANDREA DI LUCA GABRIELE DUCI DARIO ICA e Isocrate e Isocrate ICA PDA PDA VASCOLARE V D'ARTO INFERIORE D'ARTO INFERIORE e cura ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 10 di 117
11 FDGPRI72E09F205E FDAGLL51D05F205J FRRMCL73E27E573P FRNMSM72E11F205I GTNGRG55B28F205G GLLRRT72S50H501B GTTVLR75E54F205C GRLLRT52S05F205H GRNRTR55P04L245H NGRCRN64A49F205V FADIGATI PIERO FAVA GUGLIELMO FERRARO MARCELLO FRANCESNI MASSIMO GAETANI GIORGIO GALLETTI ROBERTA GATTORONERI VALERIA GIRALDI ALBERTO GUARINO ARTURO INGRAFFIA CATERINA ICA e Isocrate Isocrate ICA PDA PDA D'ARTO INFERIORE D'ARTO INFERIORE ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 11 di 117
12 LMDGNN70A12F205F LDASNS64H17I452P LNZDRD72M26C744K LZZFBA64H20H501M LPRMRZ65C05G288S MRCNTN55H03A271E MRLBNM49T02F205C MZZMLG73B10F205D MNELRA77T57F205M LA MAIDA GIOVANNI ANDREA LADO STANISLAO LANZANI EDOARDO LAZZARO FABIO LOPRESTI MAURIZIO MARCHESONI ANTONIO MARELLI BRUNO MAZZA EMILIO LUIGI MEANI LAURA MMENTN58M11F704U MEMEO ANTONIO ICA e Isocrate ICA E RIABILITATIVA (Reumatologia) PDA ICA e (Reumatologia) Isocrate PDA D'ARTO INFERIORE D'ARTO INFERIORE ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 12 di 117
13 MSSJCH66M54Z110T MSGBNR54P28E956T MNDGTN59A25F205C LDNSLV74P46D1980 MESSINA JANE MISAGGI BERNANRDO MONDINI TRISSINO AGOSTINO OLDANI SILVIA PNNLLNZ57S23A859G PANELLA LORENZO PRRLCU76M03C933O PRRMTM60T09F205J PDRDGL53D06B049W PLLNNV62T03F205D PRTLRA65R59F205A PARRAVICINI LUCA PARRINI MATTEO MARIA PEDRINI VIRGILIO PELLEGRINI ANTONIO PERETTO LAURA ICA e Isocrate Isocrate Isocrate ICA ICA PDA PDA PDA D'ARTO INFERIORE D'ARTO INFERIORE D'ARTO INFERIORE ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 13 di 117
14 PRNDTR57L59E819N PVTMRC58C07H657R RCLDNL56P56F205J RGNMLB52L14E591C SRTMRG56L05F205Y SCHLLL55T10F205K SNGLGU50C29A429D TSSLRT54D28F205U TNTGZN54L02F205C TMBLSN75L21E063E PERONI DONATA PIVETTA MARCO RECALCATI DANIELA REGONDI EMILIO ALBERTO SARTORIO AMATORE GIANLUIGI PAOLO SESARI LIONELLO SINIGAGLIA LUIGI TASSI ALBERTO TINTI GRAZIANO TOMBA ALESSANDRO ICA E RIABILITATIVA (Reumatologia) ICA e Isocrate PDA D'ARTO INFERIORE ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 14 di 117
15 TMMMSM54A20F205U TOMMASINI MASSIMO TRZPLA75E01I274D TRZMCL65P06A122X DRZGCR72D21F205W VLVGRG57E03F205G DNTLRT58C15F205I VRDFBA57L10L388G VGNNNE57C28F205M VLNLRA72H58F205N VLPRCR65D03F205Q TREZZA PAOLO TRUZZI MARCELLO CLAUDIO UDERZO EUGENIO CORRADO VALVASON GIORGIO VENTURA ALBERTO VERDONI FABIO VIGNALI ENNIO VOLONTE' LAURA VOLPONI RICCARDO ICA e Isocrate PDA D'ARTO INFERIORE ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 15 di 117
16 WLFNRG56H21F205E ZCCPTR63E23C535R WOLF ANDREA ZACCONI PIETRO NDRRRT62T29A660Z ANDRIANI ROBERTO (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, OTOCP ACUSTICHE BAIKSC77R45F205L BAI KATIUSCIA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta ICA Nuova, BNDMNC63A57F205O BANDINI MONICA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta NEUROPSIATR Nuova, NEUP IA INFANTILE BGTGFR57H23F205V BIGATTI GUIDO FRANCESCO (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta MALATTIE Nuova, DELL'APPARATO MARES NO VMD CRTNDA68B68L746V CERUTTI NADIA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta ENDOCRINOLOGI Nuova, A ENDOCD MICROINFUSORI per insulina CBLSFN61B03F205W COBELLI STEFANO (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, ONCOLOGIA ONC CMONNL69M07D969A COMI ANTONIO LORENZO (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta MALATTIE Nuova, DELL'APPARATO RESVMD CPPFNC52T53F205K COPPADORO FRANCA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta ICA Nuova, ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 16 di 117
17 DMTMST57R63C351B DIMAIUTA MARIASTELLA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, ONCOLOGIA ONC FRNGRL59S51L682X FARINA GABRIELLA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, ONCOLOGIA ONC FTNVCN59P68F499D FETONI VINCENZA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, GRTLNE82S68F205G GARATTINI ELENA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta MALATTIE Nuova, DELL'APPARATO RESVMD GFFNDR54R27F704P GUFFANTI ANDREA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, EMATOLOGIA EMA GLTMRP56H45L331I GULOTTA MARIA PIA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta NEUROPSIATR Nuova, NEUP IA INFANTILE LVRNLM67T71B429I LA VERDE NICLA MARIA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, ONCOLOGIA ONC LNGLSI71H66F205M LONGO LISA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta MALATTIE Nuova, DELL'APPARATO RESVMD MNTMCR58R70F205J MANTICA MARIA CRISTINA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, ONCOLOGIA ONC MRPPSL71H67F205B MORPURGO PAOLA SILVIA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta ENDOCRINOLOGI Nuova, A ENDCDPDA MICROINFUSORI per insulina e cura PIEDE DIABETICO ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 17 di 117
18 TTLLRT52L16G224C OTTOLINI ALBERTO (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta NEUROPSIATR Nuova, NEUP IA INFANTILE PNDMRC54M07A390K PANDOLFI MARCO (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, PEDIATRIA PED NO VMD PRSLNE57S64F205H PARISIO ELENA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, EMATOLOGIA EMA PDRGNN65C47D251I PEDERSOLI GIOVANNA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta ICA Nuova, PDRDNT52P55C933V PEDRETTI DONATA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, ONCOLOGIA ONC PRRSLV59S64L682D PERRONE SILVIA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, ONCOLOGIA ONC RMPPRM51S26C839Q RAMPINI PIETRO AMATORE (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta ENDOCRINOLOGI Nuova, A ENDCDPDA MICROINFUSORI per insulina e cura PIEDE DIABETICO RNDLSN77E57F839L RANDAZZO ALESSANDRA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta ICA Nuova, RVJRSL53T63F205A ROVEJ ROSSELLA ANGELA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, ONCOLOGIA ONC SGRLLN64S50F205K SGARBI LILIANA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta ICA Nuova, ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 18 di 117
19 SNISMN65H52I205H SIANI SIMONA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta NEUROPSIATR Nuova, NEUP IA INFANTILE TRMGNN56B29T533F TERMINE GIOVANNI (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta Nuova, OTOCP ACUSTICHE TRNMLN55C56F205Q TRONCI MARILENA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta MALATTIE Nuova, DELL'APPARATO MARES NO VMD VLNVRE57C47F257W VALENTI VERA (Ospedale Fatebenefratelli e Oftalmico) C.so di Porta NEUROPSIATR Nuova, NEUP IA INFANTILE MGRNGL48M07I535O MAGRO ANGELO GINO (Ospedale Macedonio Melloni) Macedonio GINECOLOGIA ED Melloni, OSTETRICIA GIN NDRRLD61B27F205J ANDREOLI ARNALDO (Ospedale Sacco) G.B. Grassi MALATTIE DELL'APPARATO RESVMD BSSFRC57P02F205S BASSI FERRUCCIO (Ospedale Sacco) G.B. Grassi BNDTMS81H25C933E BINDA TOMMASO (Ospedale Sacco) G.B. Grassi BLSGPP66H01E507P BOLIS GIUSEPPE (Ospedale Sacco) G.B. Grassi BRTCST56M46F205N BORTOLAMI CRISTINA (Ospedale Sacco) G.B. Grassi ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 19 di 117
20 BTTLSN58A25F205Z BOTTERO ALESSANDRO (Ospedale Sacco) G.B. Grassi OTOCP ACUSTICHE BTTFDN56A17F205P BOTTONI FERDINANDO (Ospedale Sacco) G.B. Grassi OFTALMOLOGIA OCU NO CRV BRSDVD72T25F704U BRIOS DAVIDE (Ospedale Sacco) G.B. Grassi CSTLCU62R70E801Z CASTELLI LUCIA (Ospedale Sacco) G.B. Grassi ICA CHBNCN59T59F205Y CHEBAT ENRICA (Ospedale Sacco) G.B. Grassi ENDOCRINOLOGI A ENDOCD MICROINFUSORI per insulina CHRPMR56L47F205H ARI PAOLA (Ospedale Sacco) G.B. Grassi OFTALMOLOGIA OCU NO CRV CSLMGL58R50E801T CISLAGHI M. GIULIANA (Ospedale Sacco) G.B. Grassi DMNMGN53P46G224J DAMIANI EUGENIA (Ospedale Sacco) G.B. Grassi ONCOLOGIA ONC DVDLSN74R26F205K DAVID ALESSANDRO (Ospedale Sacco) C.so di Porta Nuova, OFTALMOLOGIA OCU NO CRV DNGSFN62B16A783O DE ANGELIS STEFANO (Ospedale Sacco) G.B. Grassi OFTALMOLOGIA OCU NO CRV ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 20 di 117
21 DCEMSO70H09G751J DE IACO MOSÈ (Ospedale Sacco) G.B. Grassi ANESTESIA E RIANIMAZIONE ANR NO VMD DNEMHL80L08L219T DE NOIA MICHELE (Ospedale Sacco) G.B. Grassi DRGMLN54E45M109O DRAGHI ELENA (Ospedale Sacco) G.B. Grassi OFTALMOLOGIA OCU NO CRV FRRSRN68M45F205C FERRARIO SABRINA (Ospedale Sacco) G.B. Grassi ONCOLOGIA ONC FNOFRZ65M18H264E FOIENI FABRIZIO (Ospedale Sacco) G.B. Grassi GMBNRT69L64B300P GAMBARO ANNA (Ospedale Sacco) G.B. Grassi ONCOLOGIA ONC MRNMRC56B65I441G MERONI MARIA RACHELE (Ospedale Sacco) G.B. Grassi MSSDGN59H22F205S MESSENIO DARIO EUGENIO (Ospedale Sacco) G.B. Grassi OFTALMOLOGIA OCU NO CRV MLDFNC77L64A794P MOIOLI FRANCESCA (Ospedale Sacco) G.B. Grassi MRTMLN60S67L682L MURATORI MILENA (Ospedale Sacco) G.B. Grassi ENDOCRINOLOGI A ENDOCD MICROINFUSORI per insulina ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 21 di 117
22 NGRGGS56A29F205J NEGRETTO GIANGIUSEPPE (Ospedale Sacco) G.B. Grassi MALATTIE DELL'APPARATO RESVMD RFNPLA62C71F839Z OROFINO PAOLA (Ospedale Sacco) G.B. Grassi NEUROPSIATR IA INFANTILE NEUP SOIMRZ59A17F205Y OSIO MAURIZIO (Ospedale Sacco) G.B. Grassi PRVMRN58R68F205K PARAVICINI MARINA (Ospedale Sacco) G.B. Grassi MALATTIE DELL'APPARATO MARES NO VMD PSCNLT66M65A662Q PASCARELLI NICOLETTA (Ospedale Sacco) G.B. Grassi PCSMRC61A43F205M PECIS MARICA (Ospedale Sacco) G.B. Grassi MALATTIE DELL'APPARATO RESVMD PRRNNL67H63F205R PERRI ANTONELLA (Ospedale Sacco) G.B. Grassi NEUROPSIATR IA INFANTILE NEUP PZZSMN63M47F205Y PIAZZA SIMONA (Ospedale Sacco) G.B. Grassi PRNPCR55R31F205Z PRINA PAOLO CARLO (Ospedale Sacco) G.B. Grassi QRCSDR59D57F205O QUERCIOLI SANDRA (Ospedale Sacco) G.B. Grassi NEUROPSIATR IA INFANTILE NEUP ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 22 di 117
23 RCHRRT63S24H717Y RECH ROBERTO (Ospedale Sacco) G.B. Grassi ANESTESIA E RIANIMAZIONE ANR NO VMD RZZMRZ54P22F205V RIZZI MAURIZIO (Ospedale Sacco) G.B. Grassi MALATTIE DELL'APPARATO RESVMD RNCMCT51B44F205I RONCORONI CATERINA (Ospedale Sacco) G.B. Grassi NEUROPSIATR IA INFANTILE NEUP RSSSNN63A54F100Y RUSSO SUSANNA (Ospedale Sacco) G.B. Grassi NEUROPSIATR IA INFANTILE NEUP SLVGMC68D09F205Y SALVADORI DEL PRATO GIULIANO CESARE (Ospedale Sacco) G.B. Grassi SNDGCR56H46D969K SANDRONE GIULIA (Ospedale Sacco) G.B. Grassi (Cardiologia) SRTLSN76M46A944R SARTANI ALESSANDRA (Ospedale Sacco) G.B. Grassi e cura SCRNRN64S12A010S SCARAMUZZA ANDREA (Ospedale Sacco) G.B. Grassi PEDIATRIA PEDCD MICROINFUSORI per insulina STRGNN60T14F952X STAURENGHI GIOVANNI (Ospedale Sacco) G.B. Grassi OFTALMOLOGIA OCU NO CRV TGLBCM52C57F205D TAGLIABUE BIANCAMARIA (Ospedale Sacco) G.B. Grassi NEUROPSIATR IA INFANTILE NEUP ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 23 di 117
24 GLNCTT64S67L038N UGOLINI COSETTA (Ospedale Sacco) G.B. Grassi ICA VLLBBR73T51F205B VALLI BARBARA (Ospedale Sacco) G.B. Grassi NEUROPSIATR IA INFANTILE NEUP ZMBGTN58L18G388X ZAMBELLI AGOSTINO (Ospedale Sacco) G.B. Grassi (Malattie Infettive) RSALNE71P66D150J ARISI ELENA (Ospedale V. Buzzi) Castelvetro OTOIC ACUSTICHE e ESOPROCESSO RI IMPIANTO BNLFNT52A09E219Z BONALUMI FABIO (Ospedale V. Buzzi) Castelvetro VASCOLARE V e cura BNGVCN54C03F924D BUONAGURO VINCENZO (Ospedale V. Buzzi) Castelvetro CPRGLC70C17L872S CAPRA GIANLUCA (Ospedale V. Buzzi) Castelvetro OTOIC ACUSTICHE e ESOPROCESSO RI IMPIANTO CRLTZN61D52F205H CARLETTI TIZIANA (Ospedale V. Buzzi) Castelvetro CZZLSN52R04F205O CAZZAVILLAN ALESSANDRO (Ospedale V. Buzzi) Castelvetro OTOIC ACUSTICHE e ESOPROCESSO RI IMPIANTO CSRLCC73R70F205E CESARIS LUISA CECILIA (Ospedale V. Buzzi) Castelvetro ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 24 di 117
25 CLMLFB63R10F205G COLOMBO LUCA FABIO (Ospedale V. Buzzi) Castelvetro CLMRNT48R05F205V COLOMBO RENATO (Ospedale V. Buzzi) Castelvetro OFTALMOLOGIA OCU NO CRV FRLNDR56S02D458N FRRSFN69L41B300T LSTGLC58P06H501D MNDNNA64C50F205U FAROLFI ANDREA FERRARIO STEFANIA LISTA GIANLUCA MANDELLI ANNA (Ospedale V. Buzzi) (Ospedale V. Buzzi) (Ospedale V. Buzzi) (Ospedale V. Buzzi) Castelvetro Castelvetro Castelvetro Castelvetro PEDIATRIA ANESTESIA E RIANIMAZIONE PEDIATRIA ANESTESIA E RIANIMAZIONE PEDVMD ANRVMD PEDVMD ANRVMD MNFSRG66D07G273Q MONFORTE SERGIO (Ospedale V. Buzzi) Castelvetro MTTFNC55H08D030K MOTTA FRANCESCO (Ospedale V. Buzzi) Castelvetro PZZMSM66C24E463U PIZZUTO MASSIMO (Ospedale V. Buzzi) Castelvetro (Malattie Infettive) RZZFNC55T07H026B RIZZI FRANCO (Ospedale V. Buzzi) Castelvetro ICA ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 25 di 117
26 SOIDNL66E43I166T SOI DANIELA (Ospedale V. Buzzi) Castelvetro AUDIOLOGIA OTOIC ACUSTICHE WLFNRM69C24F205M ZOILNE59E67A818C WOLFLER ANDREA MICHELE ZOIA ELENA (Ospedale V. Buzzi) (Ospedale V. Buzzi) Castelvetro Castelvetro ANESTESIA E RIANIMAZIONE ANESTESIA E RIANIMAZIONE ANRVMD ANRVMD DNARRT53P11F205E ADONE ROBERTO ICA PDA D'ARTO INFERIORE GRTNNM59P13F205R AGRATI ANTONIO MARIA MBRGCR49T08F205Z AMBROGI GIANCARLO e cura RCNLSU56H50F205I ARCANGELI LUISA MALATTIE DELL'APPARATO RESVMD RTLSVT66A10C351M ARTALE SALVATORE ONCOLOGIA ONC SNAPNG50E30G291J ASENI PAOLO ANGELO e cura STRMGR61M47A182V ASTORI MARIA GRAZIANA NEUROPSIATR IA INFANTILE NEUP ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 26 di 117
27 BRBPRM54M16A479K BARBANO PIER REMIGIO VASCOLARE V e cura BRTNRL68P06F205J BERETTA ANDREA LUIGI BRTGNN56T46L682F BERETTA GIOVANNA ICA PDA D'ARTO INFERIORE BRTGBT74L09AP40Y BERTANI GIAMBATTISTA EMATOLOGIA EMA BRTFRC65R17I608E BERTUZZI FEDERICO DIABETOLOGIA DIACD MICROINFUSORI per insulina BGHKNN52D45F205Y BIGHELLINI KATIA BNRMRC56D26F205Z BONIARDI MARCO e cura BNOBNC59D18L781C BONO BRUNO CARLO BNMSFN77C29F205V BONOMI STEFANO PLASTICA PL e cura BNMMTN52C23F205S BONOMO MATTEO ANDREA DIABETOLOGIA DIACD MICROINFUSORI per insulina ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 27 di 117
28 BRZNNA75P57F205N BRIZIO ANNA EMATOLOGIA EMA BLGPVL48T06F205B BULGHERONI PAOLO MALATTIE DELL'APPARATO MARES NO VMD CDLRRT53T02F205K CADLOLO ROBERTO CLAPRZ63H41F205X CALIA PATRIZIA RITA CRMMNN77B48F205Z CARAMELLA MARIANNA EMATOLOGIA EMA CSSDRN60M42G224T CASSINIS ADRIANA ICA CTNLSN56C08F205Q CATENACCI ALESSANDRO GINO CSRGZR55M10H501F CAUSARANO IGNAZIO RENZO CHRMHL64H02H926Q ERICOZZI MICHELE CHSVSN59L30I690D USA IVAN SANTE MALATTIE DELL'APPARATO ANESTESIA E RIANIMAZIONE RESVMD ANR NO VMD ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 28 di 117
29 CCCLNS64E07Z133L CICCONE ALFONSO CMNGNN60A27I625T CIMINO GIOVANNI MALATTIE DELL'APPARATO MARES NO VMD CRLSVT57H03G751P CIRIOLO SALVATORE ICA PDA D'ARTO INFERIORE CTTNNL59M42F704G CITTERIO ANTONELLA MARISA PLASTICA PL e cura CLRPCT46D46F205X CLERICI PAOLA CATERINA NEUROPSIATR IA INFANTILE NEUP CDCLRF60E14F205Q CODECASA LUIGI RUFFO MALATTIE DELL'APPARATO MARES NO VMD CNODNL53E10Z602F COEN DANIELE CLLGNN58L07L500W COLELLA GIOVANNI e cura CRSSFN58B17F205K CRESPI STEFANO MALATTIE DELL'APPARATO MARES NO VMD DLLDVD75P03A859L DALLA COSTA DAVIDE ICA PDA D'ARTO INFERIORE ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 29 di 117
30 DNGRND61D15D653M DE ANGELIS ARMANDO PLASTICA PL e cura DGCCTN56P07G273H DEGIACOMO COSTANTINO PEDIATRIA PED NO VMD DSTLGN65A53F205E DISOTEO OLGA EUGENIA DIABETOLOGIA DIACD MICROINFUSORI per insulina FCCDNT59T30H560Z FACCHETTI DANTE FRRGNN57R03F205F FERRARO GIOVANNI FRINTN54R22L245Y FIORE ANTONIO FRNMDP58A02L049S FORNARO EMIDDIO POMPEO NEUROPSIATR IA INFANTILE NEUP FRNLNM54C21F205K FRANZETTI LUIGINO MAURIZIO e cura GCMMTT67L26F205Q GIACOMINI MATTEO ANESTESIA E RIANIMAZIONE ANR NO VMD GRDFRC83T14F952G GIARDA FEDERICO ICA PDA D'ARTO INFERIORE ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 30 di 117
31 GRGPRD73C28B149P GIORGI PIETRO GRRVLR78C02C933U GIRARDI VALERIO Protesi mammaria GCCNGL57C22B521F GUCCIONE ANGELO LRDLRA72E47G273R ILARDI LAURA PEDIATRIA PED NO VMD MBSFNC70D47F205W IMBESI FRANCESCA NNLLSN69A23D612C INNOCENTI ALESSANDRO PLASTICA PL e cura JKBBBR52B54Z127S JAKUBOWICZ BARBARA HANN PLASTICA PL e cura LSGGRD59T60F205S LASAGNA GAIA PLASTICA PL e cura LNGCLM53L05I849F LONGO CARLO MARIA MNCLCU78H15M102P MANCINI LUCA PEDIATRIA PED NO VMD ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 31 di 117
32 MNRCLD54S06F205L MANERA CLAUDIO ICA MNTGRL67H48A182P MANTINI GABRIELLA MAURI OTOIC ACUSTICHE e ESOPROCESSO RI IMPIANTO MRNNZE56L12F205R MARINONI ENZO MRZMHL71S65E951V MARZORATI MICHELA NATALINA Cherasco NEUROPSIATR IA INFANTILE NEUP MSPFBA61A18I625P MASPERO FABIO MRNLRT66C30F205Q MERONI ALBERTO MARCO MNGGPP62A29F205E MINGOIA GIUSEPPE OTOIC ACUSTICHE e ESOPROCESSO RI IMPIANTO MNILNE67H53F205D MION ELENA ENDOCRINOLOGI A ENDOCD MICROINFUSORI per insulina MTTGNP54S28F205J MIOTTI GIULIANO PIETRO e cura MRNMHL66B15F205X MIRANDA MICHELE ROBERTO ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 32 di 117
33 MNTGDU55C27F205N MONTANARI GUIDO MALATTIE DELL'APPARATO MARES NO VMD MNTLDI61M45F205P MONTEMURRO LIDIA MRNMRA61L18I138P MORONI MAURO ONCOLOGIA ONC MSCMRC60R11H501D MOSCATI MARCO NGRSPH46E14Z129F NEGREANU JOSEPH PLASTICA PL e cura NGRMTM56E49F205S NEGRI MARTA NBLLNI65B14C933X NOBILI LINO NEUROIOPATO LOGIA NEUVMD OSAS - per la Sindrome delle Apnee Ostruttive del Sonno e altre LROSFN55P17L020A OLEARI STEFANO PNALNI68M52Z129Z PAUNA IULIANA e cura PRTMRC60B10B354R PERETTI MARCO PEDIATRIA PED NO VMD ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 33 di 117
34 PCCMCL53T48F839J PICCOLO IMMACOLATA ICA PNTBSL81M27F158K PINTAUDI BASILIO PZZLNE50C58G478N PIOZZI ELENA PZZGLG57L25F205Z PIZZI GIANLUIGI PLCNGL64L14I158T PLACENTINO ANGELO PRTLSN55S66F205O PROTTI ALESSANDRA ENDOCRINOLOGI A OFTALMOLOGIA ENDOCD OCUCI ENDOCRINOLOGIA ENDOCD OTOIC MICROINFUSORI per insulina CRV - RIABILITAZIONE FUNZIONE VISIVA MICROINFUSORI p ACUSTICHE e ESOPROCESSO RI IMPIANTO RPSVCN47A02G371M RAPISARDA VINCENZO MARIA PLASTICA PL e cura RDLTZN48L58F205I REDAELLI TIZIANA ICA RGNPRZ56H52F205V REGONDI PATRIZIA OFTALMOLOGIA OCUCI CRV - RIABILITAZIONE FUNZIONE VISIVA RNGMNC69P52G453E RENGA MONICA ONCOLOGIA ONC ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 34 di 117
35 RBRSNO64L49F205K RIBERA SONIA EMATOLOGIA EMA RGMMNG59P48C566Y RIGAMONTI MARIA ANGELA OFTALMOLOGIA OCUCI CRV - RIABILITAZIONE FUNZIONE VISIVA RNLGPL57H10F205D RINALDI GIANPAOLO RNLMCL54M19F205D RINALDI MARCELLO MALATTIE DELL'APPARATO MARES NO VMD RLIFNC56M11F205W RIOLO FRANCO VASCOLARE V e cura RLOJCN52T62Z133C ROLO JOYCE ANGELA AL MALATTIE DELL'APPARATO RESVMD RNZMFR52M21F205O RONZONI MAURO FRANCO RSOGNN64S06F205P ROSA GIOVANNI OTOIC ACUSTICHE e ESOPROCESSO RI IMPIANTO RSSRLL55E52F205A ROSSETTI ORNELLA MARINA e cura RSSHCV59H25F205X ROSSI ARDIZZONE MARCO e cura ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 35 di 117
36 SNTSVN51H70F205M SANTAMBROGIO SILVIA ANNA OFTALMOLOGIA OCUCI CRV - RIABILITAZIONE FUNZIONE VISIVA SNTNTN71E11C523B SANTORO ANTONIO NEUROPSIATR IA INFANTILE NEUP STTFNN75L63G224Q SETTEMBRINI FERNANDA PLASTICA PL e cura SRNVNI55E21F205U SIRONI IVANO e cura TRNMLN67B68F205U TARENZI EMILIANA ONCOLOGIA ONC TSORFL62S62D198Z TOSI RAFFAELLA ICA TRZSNL59T51H501I TREZZA SERENELLA NEUROPSIATR IA INFANTILE NEUP VCCRRT51E19F205Z VACCARI ROBERTO NEUROPSIATR IA INFANTILE NEUP VLNMRT63P22F205B VALENTINOTTI UMBERTO ALESSAN VGNLCU74R66E507A VIGANO' LUCIA NEUROPSIATR IA INFANTILE NEUP ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 36 di 117
37 ZCCMLR54B52D969L ZUCCARINO MARIA LAURA NEUROPSIATR IA INFANTILE NEUP MRSLCU68E18F205C AMORESANO LUCIO le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ENDOCRINOLOGI A ENDOCD MICROINFUSORI per insulina BCCLCU61D23G920B BAIOC LUCA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ICA BXAMCL49T55F205V BAX MARCELLA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") (Cardiologia) BTTSNM64C4F205N BETTAZZA SIMONA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") e cura BSLNNT60R49Z326P BISOL ANTONIETTA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") BRRRND55L44D150F BORRELLI ARMANDA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD BZZMRN57A59F205V BOZZONI MARINA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") CMAMRN67T57F205C CAIMI MARINA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") CVGGPL58A26F205T CAVIGIOLI GIAMPAOLO le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") MALATTIE DELL'APPARATO RESVMD ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 37 di 117
38 CHRMNG62M65X224F RICO MARIANGELA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") (Cardiologia) CFTMRN62C71F205F CIOFETTI MORENA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") CLMSFN61T31F205E CLEMENTE STEFANO le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD CNCLCL53P56Z103R CONCOREGGI ELSA CLEMENTINA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD CRSLSN59P64D969F CORSI ALESSANDRA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") NEUROPSIATR IA INFANTILE NEUP DNVMNN78E71D286R DENOVA MARIANNA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") e cura FRRFLV52D67I690Q FERRARINI FULVIA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") FRSNTN53D05E783Y FORESI ANTONIO le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") MALATTIE DELL'APPARATO RESVMD FRUMLL53E41F888X FURIA MIRELLA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD GBRMRN56C67F205X GABRIONE MARINA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 38 di 117
39 GVGMGL67P63F205U GIOVAGNONI MARIA GLORIA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") GRODNL51E59I690D GORI DANIELA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") LVYDLL51M47Z352G LEVY DANIELLA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") LVRCRM66R60F205K LIVERANI ARA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD LNGMHL57H61F205I LONGHINI MICHELA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD MRCGNN57C24F704Q MARCHETTI GIOVANNI le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD MRLSLV57T44F704E MARELLI SILVIA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD MRNNRL69T53Z115U MSTBRD56M15I158P MARINOU ANDROULA MASTROPASQUA BERARDINO le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") MALATTIE DELL'APPARATO MALATTIE DELL'APPARATO RESVMD RESVMD MZZPLA57S51F205P MAZZA PAOLA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 39 di 117
40 MZZTNB54A48F205O MAZZOLA TIZIANA BIANCA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD MSOGRL49P66F205H MOISE GABRIELLA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD MSONLT68B48Z129V MOISE NICOLETTA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") GINECOLOGIA ED OSTETRICIA MNTBBR75A68I625T MONTI BARBARA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") GINECOLOGIA ED OSTETRICIA MNZBBR63E70F205A MONZIO COMPAGNONI BARBARA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") NSSCST57L50F205G NASSIVERA CRISTINA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") OFTALMOLOGIA OCU NO CRV GGNFNC54R05F205Z OGGIONI FRANCESCO le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD PLCNDR56B02F205Z PELUC ANDREA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") MALATTIE DELL'APPARATO MARES NO VMD PGGCRM78E61F704N POGGI ARA MARIA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") GINECOLOGIA ED OSTETRICIA PLOVNC63B01D332W POLO VINCENZO le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ENDOCRINOLOGI A ENDOCD MICROINFUSORI per insulina ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 40 di 117
41 RSSRST70T44M052X ROSSI RITA STELLA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") GINECOLOGIA ED OSTETRICIA SPRFTT58R13F205D SAPORITI FABIO ETTORE le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") e cura SGRCRL57R49I690D SGORBATI CARLA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") SGNGDN53P23D286T SIGNORELLI GIORDANO le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") (Cardiologia) TGLNNA57E66B156Y TAGLIAVINI ANNA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") NEUROPSIATR IA INFANTILE NEUP TZZSLS68D46F205S TAZZARI SARA ELISABETTA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") TRVMLD58T65F205H TRIVELLA MATILDE le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ANESTESIA E RIANIMAZIONE ANR NO VMD TRRGPP51T15L175G TURRA GIUSEPPE le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") e cura TZNGRG51E10Z115N TZANNIS GIORGIO le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") GINECOLOGIA ED OSTETRICIA VLNGST50C67G019S VALENTINI AUGUSTA le Matteotti 83 - ASST Nord (Presidio Ospedaliero "Città di Sesto SG") ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 41 di 117
42 LJALSN70C27F205K ALOJA ALESSANDRO ASST Nord (Presidio RLAMGH81P56F205Q ARIOLI MARGHERITA ASST Nord (Presidio GERIATRIA GER RSALNE71P66D150J ARISI ELENA ASST Nord (Presidio OTOIC ACUSTICHE e ESOPROCESSO RI IMPIANTO BLBNBT59B59Z315H BELAI BEYENE NEBIAT ASST Nord (Presidio BNDNLL71M41F205H BENEDETTI NICOLE ELISA ASST Nord (Presidio GERIATRIA GER BTTLGL57H52F205K BETTAZZI LAURA GIULIA ASST Nord (Presidio BNCFBA56R22F205C BIAN FABIO ASST Nord (Presidio e cura BNMNRC56D13G388Y BONOMI ENRICO ASST Nord (Presidio e cura BRTDRA70S24E205B BOROTTO DARIO ASST Nord (Presidio UROLOGIA URO BRRPQL77P25F839R BORRIELLO PASQUALE ASST Nord (Presidio ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 42 di 117
43 BRSLCL55B07D193G BRESSAN LIVIO CLAUDIO ASST Nord (Presidio BRVFNN55B21F704M BRIVIO FERNANDO ASST Nord (Presidio e cura CCPLIA56R68F205L CACOPARDO LIA ASST Nord (Presidio CGNNLS61L48F205C CAGNANA ANNALISA ASST Nord (Presidio ICA CLLLEI54T06F205N CALLONI ELIO ASST Nord (Presidio CNDLMR56P11F205N CANDELA LUIGI MARIA ASST Nord (Presidio OFTALMOLOGIA OCU NO CRV CNVPLA73C52F205B CANOVARO PAOLA ASST Nord (Presidio CPRSLV70M55A539F CAPOROTUNDO SILVIA ASST Nord (Presidio GERIATRIA GER CRSLRA79S47E463I CARASSALE LAURA ASST Nord (Presidio GERIATRIA GER CRLGNN52R16B180K CARLUCCIO GIOVANNI ASST Nord (Presidio OTOCP ACUSTICHE ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 43 di 117
44 CSGNRD66C30F205L CASAGRANDE ANDREA ASST Nord (Presidio e cura CSTLCU73S01F205Y CASATI LUCA ASST Nord (Presidio OTOCP ACUSTICHE CREPTR55P11E317Y CEREA PIETRO ASST Nord (Presidio CRLGRL69M03B354S CIRILLO GABRIELE ASST Nord (Presidio ICA CLZMRC64E15F704E COLZANI MARCO ASST Nord (Presidio e cura CRCFNC74H27F205E CROCE FRANCESCO ASST Nord (Presidio DPSGNN72L24C351R DE PASQUALE GIOVANNI ASST Nord (Presidio GERIATRIA GER DDNNCL60R15F205P DI DINO NICOLA ASST Nord (Presidio OFTALMOLOGIA OCU NO CRV RGLCRL77S44F205H ERGOLI CLARA LORA ASST Nord (Presidio ANESTESIA E RIANIMAZIONE ANR NO VMD FNTVTR65T15F205H FONTANA VITTORIO ASST Nord (Presidio GERIATRIA GER ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 44 di 117
45 FRNSLV72E61E094U FURIANI SILVIA ASST Nord (Presidio (Nefrologia) FSRNRF71M22E951I FUSARO ANDREA F. ASST Nord (Presidio GLLPLA74D59I625L GALLI PAOLA ASST Nord (Presidio ENDOCRINOLOGI A ENDCDPDA MICROINFUSORI per insulina e cura PIEDE DIABETICO GRZRSL62H43F004Z GAROZZO ROSALIA ASST Nord (Presidio ICA GVGDNC54P06F205A GAVEGLIO DOMENICA ASST Nord (Presidio NEUROPSIATR IA INFANTILE NEUP GBRFWN59L61Z368X GEBRU KAHSAY FREWOINI ASST Nord (Presidio OFTALMOLOGIA OCU NO CRV GBRLCR61L18F704Y GIUBERTI ALFIO CARLO ASST Nord (Presidio UROLOGIA URO LZZFVN65B21F704D LEZZIERO FLAVIO ASST Nord (Presidio e cura LCHGCR62L23B718D LOCHE GIANCARLO ASST Nord (Presidio LNGMTD72P10F205E LONGO MATTEO ADRIANO ASST Nord (Presidio ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 45 di 117
46 LCHCLL73L69I449D LUCHESINI CAMILLA ASST Nord (Presidio ONCOLOGIA ONC MNCLGB74E43F205X MANCA THIESI DI VILLAHERMOSA ELENA GABRIELLA ASST Nord (Presidio MNCSDR56R28D869T MANCARELLA SANDRO ASST Nord (Presidio MNGPVT59T08C933W MANGHISI PIERVITTORIO ASST Nord (Presidio OTOCP ACUSTICHE MCRNDR65T18F205Y MARCHESINI ANDREA ASST Nord (Presidio MRLLCU66P04F205B MAROLDA LUCA ASST Nord (Presidio ICA MRSMTR66C53Z133H MARSILI MARIA TERESA ASST Nord (Presidio e cura MLTGLC78L13H224L MELITO GIANLUCA ASST Nord (Presidio MNGLNE74S41F205L MENEGHINI ELENA ASST Nord (Presidio ENDOCRINOLOGI A ENDCDPDA MICROINFUSORI per insulina e cura PIEDE DIABETICO MLIFNC78L55L219E MIOLA FRANCESCA ASST Nord (Presidio ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 46 di 117
47 MLTBBR67P68F205E MOLTENI BARBARA ASST Nord (Presidio e cura MNTLSV69D02F205S MONTI LUCA OSVALDO ASST Nord (Presidio OTO NO ACUSTICHE MNZNMB55A46D019U MONZANI NORMA BAMBINA ASST Nord (Presidio ANESTESIA E RIANIMAZIONE ANR NO VMD PRLLNE57M58I819O PAROLO ELENA ASST Nord (Presidio ICA PSTLSN72B60F205Q PASTA ALESSANDRA ASST Nord (Presidio UROLOGIA URO PNGSFN83D06F205M PENGO STEFANO ASST Nord (Presidio PZZPLA67E44F205H PIZZAGALLI PAOLA ASST Nord (Presidio ICA RGGSFN60R31F704A REGGIANI STEFANO ASST Nord (Presidio RCCMCM64E68B34H RICCARDI MONICA MARIA ASST Nord (Presidio OFTALMOLOGIA OCU NO CRV RCCLRT58M30F704X ROCCA ALBERTO ASST Nord (Presidio DIABETOLOGIA DIACDPDA MICROINFUSORI per insulina e cura PIEDE DIABETICO ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 47 di 117
48 SDNFLN61S20I690R SADINO FABIO ASST Nord (Presidio OFTALMOLOGIA OCU NO CRV SLASFN80S05F205F SALA STEFANO ASST Nord (Presidio SLVLSN73H45F704Y SALVIONI ALESSANDRA ASST Nord (Presidio SNTGAI70P68I625H SANTAGOSTINO BARBONE GAIA ASST Nord (Presidio (Nefrologia) SBCMNC54S68F205V SBAC MARIA CONCETTA ASST Nord (Presidio SCRRRT75R14F205Z SCARANI ROBERTO ASST Nord (Presidio ANESTESIA E RIANIMAZIONE ANR NO VMD SCCMBT52B55F205C SEC MARIA BEATRICE ASST Nord (Presidio SLSMRT73S65Z131X SOLA' SANTA OLALLA MARTA ASST Nord (Presidio SMZLCN56C67F205Q SOMAZZI LUCIANA ASST Nord (Presidio OFTALMOLOGIA OCU NO CRV SPRGFR69R31F205Z SPORTELLI GIANFRANCO ASST Nord (Presidio ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 48 di 117
49 STFPLA63D30F205L STEFANINI PAOLO ASST Nord (Presidio e cura TRVGZG58D57F205T TRAVERSO GRAZIA ASST Nord (Presidio RSUGPP53S10F943D URSO GIUSEPPE ASST Nord (Presidio e cura VLLMRC57D61F205Z VILLA MARICA ASST Nord (Presidio NEUROPSIATR IA INFANTILE NEUP WUXSNG52L20Z217Z WU SHENG N ASST Nord (Presidio ZGAMRC56R06F205N ZAGO MARCO ASST Nord (Presidio OFTALMOLOGIA OCU NO CRV ZGLLNR81L50F205E ZIGLIOLI ELEONORA ASST Nord (Presidio GERIATRIA GER BSHLAI50R13Z220N ABU SHWAIMA ALI ASST Nord (Presidio Don Orione DBMBBS56C31Z224J ADIBI MOUSAVI ABBAS ASST Nord (Presidio Doria OTOCP ACUSTICHE RLDCST53H55F704L AIROLDI CRISTINA ASST Nord (Presidio Rugabella Ripamonti OFTALMOLOGIA OCU NO CRV ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 49 di 117
50 LBNGRL59A58F205Q ALBONICO GABRIELLA ASST Nord (Presidio Puecher Quarenghi Rugabella NGLSLV60R71F205W ANGELINI SILVIA ASST Nord (Presidio Doria Stromboli e cura NSLMLS51D55E648B ANSELMI M. LUISA ASST Nord (Presidio Farini Livigno RCDLSE55H62E506S ARCADI ELISA ASST Nord (Presidio Doria Don Orione OFTALMOLOGIA OCU NO CRV SNGLRA56H52F205Y ASNAGHI LAURA ASST Nord (Presidio Livigno Masaniello OFTALMOLOGIA OCU NO CRV ZZLSVT57D11B428C AZZOLINA SALVATORE ASST Nord (Presidio Don Orione Farini Quarenghi e cura BRBSST54D29H269W BARBERA SEBASTIANO ASST Nord (Presidio Don Orione OTO NO ACUSTICHE BLAFMN64T46Z133F BAULEO FILOMENA ASST Nord (Presidio Doria Rugabella Mangiagalli BRTMNL57C52F205C BERTAZZOLI MANUELA ASST Nord (Presidio Stromboli OTOCP ACUSTICHE BNCNTN54M12D671U BIANCO ANTONIO ASST Nord (Presidio Stromboli MALATTIE DELL'APPARATO MARES NO VMD ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 50 di 117
51 BLTCLD76B01F839B BILOTTA CLAUDIO ASST Nord (Presidio Doria GERIATRIA GER BRCLCU61D13F205I BOERCI LUCA ASST Nord (Presidio Stromboli OFTALMOLOGIA OCU NO CRV BNLDNL60E46F205N BONELLI DANIELA ASST Nord (Presidio Accursio Mangiagalli OFTALMOLOGIA OCU NO CRV BSORRA52E42F205G BOSIA AURORA ASST Nord (Presidio Rugabella Molise Fantoli OTO NO ACUSTICHE BRMMNG48L58D492O BRAMANTE MARIA ANGELA ASST Nord (Presidio Mangiagalli Farini OFTALMOLOGIA OCU NO CRV BRSSGN58L08F205M BRESSI SERGIO ASST Nord (Presidio Accursio BRVFNN55B21F704M BRIVIO FERNANDO ASST Nord (Presidio Cologno Monzese e cura CFRFNC58D28H926J CAFARO FRANCESCO ASST Nord (Presidio Inganni OFTALMOLOGIA OCU NO CRV CLCRTT58A61F205S CALCINONI ORIETTA ASST Nord (Presidio Doria OTOCP ACUSTIC CNDLMR56P11F205N CANDELA LUIGI MARIA ASST Nord (Presidio Cusano Milanino OFTALMOLOGIA OCU NO CRV ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 51 di 117
52 CRDPJT53C24Z115Z CARDARAS PANAJIOTIS ASST Nord (Presidio Cologno Monzese Cusano Milanino CRNLRA76A50E801K CARNAGHI LAURA ASST Nord (Presidio Cologno Monzese GERIATRIA GER CNDMGD57A66F205Q CENDALI MADGA ASST Nord (Presidio Fantoli OFTALMOLOGIA OCU NO CRV CRNMRA67H61G388R CERNIGLIA MARIA ASST Nord (Presidio Baroni OTO NO ACUSTICHE CCRDDR74E62C351T CICERO ADELAIDE RITA ASST Nord (Presidio Gola OFTALMOLOGIA OCU NO CRV CLLLRI67D52F839E CIULLO ILARIA ASST Nord (Presidio Cusano Milanino DIABETOLOGIA DIACD MICROINFUSORI per insulina CNTRMR57D53F205Q CONTI REANA MARIA ASST Nord (Presidio Fiamma OTO NO ACUSTICHE CRBRFL58P66F205B CRABBI RAFFAELLA ASST Nord (Presidio Doria OFTALMOLOGIA OCU NO CRV DFFNNA54E63F205Q DAFFONO ANNA ASST Nord (Presidio Rugabella Accursio Molise DLZSRN49P58L378N DALZOCO SERENA ASST Nord (Presidio Doria Rugabella GERIATRIA GER ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 52 di 117
53 DMBMRC59D23B492Z D'AMBROSIO MARCO ASST Nord (Presidio Stromboli OFTALMOLOGIA OCU NO CRV DBRGNN59B50D946W DE BERTI GIOVANNA ASST Nord (Presidio Stromboli OTOCP ACUSTICHE DFLGNN57H03F205S DE FELICE GIOVANNI PAOLO ASST Nord (Presidio Inganni OFTALMOLOGIA OCU NO CRV DGRPLA61L26F205W DE GIORGIS PAOLO ASST Nord (Presidio Farini DGVNLL56B60B104J DI GIOVANNI ANGELA LUCIA ASST Nord (Presidio Doria Don Orione Mangiagalli Stromboli Fantoli Puecher DCUMSM58M31F205W DUCA MASSIMO ASST Nord (Presidio Masaniello Quarenghi OTO NO ACUSTICHE FLLSLV52R49I138T FAILLA SILVIA ASST Nord (Presidio Mangiagalli Fiamma OFTALMOLOGIA OCU NO CRV FJNJZY54D21Z127M FAJNHAKEN JERZI ASST Nord (Presidio Fantoli ICA FLLCRL58C19H501H FALLENI CARLO ASST Nord (Presidio Cusano Milanino OFTALMOLOGIA OCU NO CRV FSLDTL56P49B342X FASOLATO DONATELLA ASST Nord (Presidio Puecher Doria Molise OFTALMOLOGIA OCU NO CRV ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 53 di 117
54 FMNNNN59A01G277T FIUMANO' ANTONINO ASST Nord (Presidio Ripamonti FGLLSN68F839H FOGLIA ALESSANDRA ASST Nord (Presidio Baroni Farini Gola ICA GLLLNM63L66F205J GALLOTTI LILIANA MARIA ASST Nord (Presidio Masaniello OFTALMOLOGIA OCU NO CRV GRGLSN52A31F205V GAREGNANI ALESSANDRO ASST Nord (Presidio Accursio Quarenghi OFTALMOLOGIA OCU NO CRV GTTRSL66E57G388Y GATTI ROSSELLA ASST Nord (Presidio Doria Don Orione Rugabella Puecher GNTSLV63A65F205Q GENITRINI SILVIA ASST Nord (Presidio Baroni Fiamma GNIMLL56D52G431Y GIANA MIRELLA ASST Nord (Presidio Farini ICA GNCNLS71A66D810C GIANCATERINI ANNALISA ASST Nord (Presidio Cusano Milanino DIABETOLOGIA DIACD MICROINFUSORI per insulina GRNCRM54E64F205I GRANATIERI CLARA MARIA ASST Nord (Presidio Don Orione Cusano Milanino GRGLRD55B22G388E GRUGNI ALFREDO ASST Nord (Presidio Masaniello Quarenghi ICA ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 54 di 117
55 JCLNTA56T56F205A JACOEL ANITA ASST Nord (Presidio Accursio OTOCP ACUSTICHE KBRSTL63S60Z154A KOBRINA SVETLANA ASST Nord (Presidio Stromboli OTOCP ACUSTICHE KRSRTH52M60Z226A KRASEVSKY RUTH ASST Nord (Presidio Farini Gola OFTALMOLOGIA OCU NO CRV LNTRRT58C26H223J LEONETTI ROBERTO ASST Nord (Presidio Mangiagalli OFTALMOLOGIA OCU NO CRV LGDPLA69E31C352N LO GIUDICE PAOLO ASST Nord (Presidio Doria ICA in LNTCST64R62B157V LONATI CRISTINA ASST Nord (Presidio Baroni OFTALMOLOGIA OCU NO CRV LVGCLG58P04F205E LOVAGNINI SCHER CARLO AUGUSTO ASST Nord (Presidio Cusano Milanino DIABETOLOGIA DIACD MICROINFUSORI per insulina MCTMML53B13F205S MACIOTTA ROLANDIN MARIO EMILIO BRUNO ASST Nord (Presidio Sassi OFTALMOLOGIA OCU NO CRV MGGLRI73M65B832V MAGGI ILARIA ASST Nord (Presidio Accursio Stromboli OFTALMOLOGIA OCU NO CRV MGNSLV54L58F205Z MAGNANI SILVIA ASST Nord (Presidio Farini OTO NO ACUSTICHE ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 55 di 117
56 MGNRNT59L49F205S MAGNONI RENATA ASST Nord (Presidio Livigno MGRNTL66P67F205K MAGRI NATALIA ASST Nord (Presidio Don Orione Rugabella Mangiagalli MLSGUO54A27E625S MALASOMA UGO ASST Nord (Presidio Farini OFTALMOLOGIA OCU NO CRV MNDMSM51B20F205K MANDELLI MASSIMO ASST Nord (Presidio Cologno Monzese OFTALMOLOGIA OCU NO CRV MSSCNZ67D56Z133X MASSAFRA CINZIA ASST Nord (Presidio Cologno Monzese DIABETOLOGIA DIACD MICROINFUSORI per insulina MSSNLM50S44F205I MASSARI ANGELA MARIA ASST Nord (Presidio Ippocrate OFTALMOLOGIA OCU NO CRV MLSRLL65T41E473I MELIS ORNELLA ASST Nord (Presidio Doria OTOCP ACUSTICHE MZZPRZ49S65I690O MEZZADRA PATRIZIA ASST Nord (Presidio Don Orione Puecher ICA MRDMHS50T02Z224G MIR DJAHANBAKHSH LANGROODI ASST Nord (Presidio Gola Baroni Ripamonti MRBCMN52H23D643I MIRABELLA CARMINE ASST Nord (Presidio Doria ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 56 di 117
57 MSCNLT56C55H501J MUSACO NICOLETTA ASST Nord (Presidio Cusano Milanese DIABETOLOGIA DIACD MICROINFUSORI per insulina NCSFPP58H02M088K NICOSIA FILIPPO ASST Nord (Presidio Doria OTOCP ACUSTICHE CCHNNN55D08H224H OCPINTI ANTONINO SALVATORE ASST Nord (Presidio Masaniello Inganni e cura LROSFN55P17L020A OLEARI STEFANO ASST Nord (Presidio Accursio RSTLGR64M12F205T ORESTILLI ALDO GIORGIO ASST Nord (Presidio Fantoli PNZMRZ49L11F205A PANIZZI MAURIZIO ASST Nord (Presidio Ippocrate OFTALMOLOGIA OCU NO CRV PDRMNC68H41F205L PEDRAZZOLI MONICA ASST Nord (Presidio Puecher PRTTZN56A54B300C PERTONI TIZIANA ASST Nord (Presidio Stromboli Gola AUDIOLOGIA OTOCP ACUSTICHE PRNNNL60A43F205E PIERONI ANTONELLA LIVIA EVELINA ASST Nord (Presidio Gola in PZZGNN51R02F704S POZZI GIOVANNI PAOLO ASST Nord (Presidio Cusano Milanino OTO NO ACUSTICHE ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 57 di 117
58 RPNGRG58S22F952J RAPONI GIORGIO ASST Nord (Presidio Ippocrate Livigno OTO NO ACUSTICHE RBCMGR51M70D969T REBEC MARIA GRAZIA ASST Nord (Presidio Farini Sassi OTO NO ACUSTICHE RSOMRZ49E18L219L ROSA MAURIZIO ASST Nord (Presidio Fiamma SMMLSN61H14H501L SAMMARTINO ALESSANDRO ASST Nord (Presidio Doria Don Orione Puecher OFTALMOLOGIA OCU NO CRV SNTSFN61S19F952N SANTAMARIA STEFANO ASST Nord (Presidio Sassi Fantoli SRDGGF57R20F205M SARDI GIORGIO FRANCO ASST Nord (Presidio Cologno Monzese OTO NO ACUSTICHE SCHSMN68H63F839Z SOPPA SIMONA ASST Nord (Presidio Accursio GERIATRIA GER SMRGNN59E10C741X SEMERARO GIOVANNI ASST Nord (Presidio Doria Don Orione OFTALMOLOGIA OCU NO CRV SNSCNZ58T53G113P SINIS CINZIA ASST Nord (Presidio Mangiagalli Ripamonti OTO NO ACUSTICHE SPNLSN55S52F205Q SPINOLA ALESSANDRA ASST Nord (Presidio Mangiagalli Doria (Senologia) e cura ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 58 di 117
59 SPRMCN50B22F952R SPRUZZOLA MARCO ASST Nord (Presidio Ippocrate Stromboli STCLRA60B51F205U STUC LAURA ASST Nord (Presidio Masaniello OFTALMOLOGIA OCU NO CRV TSSLNG56P66F205R TASSI LUCIA ANGELICA ASST Nord (Presidio Livigno OFTALMOLOGIA OCU NO CRV TNTRMN63S12Z306Q TENTO TENTO RAYMOND ASST Nord (Presidio Doria OFTALMOLOGIA OCU NO CRV TRARCR53D11A271D TRAU' RICCARDO ASST Nord (Presidio Fiamma Ripamonti Inganni OFTALMOLOGIA OCU NO CRV TRNLRD61S13B915P TROIANO LEONARDO ASST Nord (Presidio Accursio AUDIOLOGIA OTOCP ACUSTICHE TRTLRT58M20F205S TURATI ALBERTO ASST Nord (Presidio Doria e cura TRTNDR63B20F205W TURATI ANDREA ASST Nord (Presidio Doria Don Orione MALATTIE DELL'APPARATO MARES NO VMD VLNSML51L16B619E VALENTINO SAMUELE ASST Nord (Presidio Inganni VTRNTN56H29A944O VATRELLA ANTONIO ASST Nord (Presidio Gola ICA ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 59 di 117
60 VLLPLA53D25A132M VELLETRANI PAOLO ASST Nord (Presidio Farini Livigno OTO NO ACUSTICHE VTOMGB58C69F205O VOTA MARIA GABRIELLA ASST Nord (Presidio Accursio OFTALMOLOGIA OCU NO CRV ZFFLRC57P65F205X ZAFFARONI ELEONORA ASST Nord (Presidio Ippocrate Stromboli LBRVNT84D66D938O ALBERTINO VALENTINA Carlo) Pio II, ICA LDRLSN61R12L762Q ALDROVANDI ALESSANDRO Carlo) Pio II, SNDCLD65L12F205Q AUSENDA CARLO DOMENICO Carlo) Pio II, ICA BTTLGV68D66F205Y BLLPMR62M65F205M BATTAGLIA ELVIA GIOVANNA BOLLATI PAOLA MARIA Carlo) Carlo) Pio II, Pio II, MALATTIE DELL'APPARATO ENDOCRINOLOGI A RESVMD ENDCDPDA MICROINFUSORI per insulina e cura PIEDE DIABETICO BSSFNC52T05F205S BOSSI FRANCESCO Carlo) Pio II, NEUROPSIATR IA INFANTILE NEUP BRMRSN64H51F704T BRAMBILLA ROSSANA Carlo) Pio II, ICA ATS MILANO (EX ASL DI MILANO) 13/06/2016 Pagina 60 di 117

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