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Detection of Small Airway Dysfunction in Asymptomatic Smokers with Preserved Spirometry: The Value of the Impulse Oscillometry System

International journal of chronic obstructive pulmonary disease, 2021-01, Vol.16, p.2585-2590

2021

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Relationship between quality of life and behavioural disorders in children with persistent asthma: a Multiple Indicators Multiple Causes (MIMIC) model

Scientific reports, 2020-04, Vol.10 (1), p.6957-6957, Article 6957

2020

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Effect of elexacaftor–tezacaftor–ivacaftor modulator on lung structure in cystic fibrosis

Pulmonology, 2023-09, Vol.29 (5), p.441-443

2023

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63 Respiratory infections in children with cystic fibrosis (CF). Relationship with clinical and functional features

Journal of cystic fibrosis, 2016-06, Vol.15, p.S67-S67

2016

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Insulin production and resistance in cystic fibrosis: Effect of age, disease activity, and genotype

Journal of endocrinological investigation, 2012-03, Vol.35 (3), p.246-253

2012

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203 Low dose azithromycin may slow the decline of respiratory function in cystic fibrosis

Journal of cystic fibrosis, 2011, Vol.10, p.S52-S52

2011

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P065 Use of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with rare mutations

Journal of cystic fibrosis, 2024-06, Vol.23, p.S87-S87

2024

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P156 Effects of lumacaftor/ivacaftor in CF children 2–6 years old: a case series

Journal of cystic fibrosis, 2024-06, Vol.23, p.S102-S102

2024

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WS6.9 Cystic fibrosis related diabetes (CFRD): evidence for a role of miR-155, miR-370 and miR-708

Journal of cystic fibrosis, 2014-06, Vol.13, p.S14-S14

2014

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P187 Small airways disease in cystic fibrosis patients

Journal of cystic fibrosis, 2023-06, Vol.22, p.S122-S122

2023

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P134 Prevalence of multi-drug, antimicrobial-resistant bacteria in children with cystic fibrosis

Journal of cystic fibrosis, 2022-06, Vol.21, p.S102

2022

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Six-minute walking test in cystic fibrosis adults with mild to moderate lung disease: comparison to healthy subjects

Respiratory medicine, 2001-12, Vol.95 (12), p.986-991

2001

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P131 Clinical impact of Aspergillus fumigatus in children with cystic fibrosis

Journal of cystic fibrosis, 2022-06, Vol.21, p.S101

2022

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NUTRITIONAL AND RESPIRATORY EFFECTS OF AZITHROMYCIN LONG-TERM TREATMENT IN CYSTIC FIBROSIS PATIENTS

Journal of cystic fibrosis, 2008-07, Vol.7, p.S21-S21

2008

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ePS4.07 COVID-19 early vaccination campaign in Italian cystic fibrosis (CF) patients: the experience of the Italian Society for the Study of Cystic Fibrosis (SIFC)

Journal of cystic fibrosis, 2022-06, Vol.21, p.S54-S54

2022

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IPD2.05 Effects of ivacaftor in patients with cystic fibrosis and severe lung disease carrying CFTR mutations with residual function

Journal of cystic fibrosis, 2018-06, Vol.17, p.S54-S55

2018

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WS13.6 Urinary incontinence in adult patients with cystic fibrosis: prevalence, impact on daily life and relationship with chronic cough

Journal of cystic fibrosis, 2018-06, Vol.17, p.S25-S25

2018

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P157 Role of osteopathic manipulative treatment in cystic fibrosis: a pilot study

Journal of cystic fibrosis, 2018-06, Vol.17, p.S103-S103

2018

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P134 SARS-CoV-2 infection in cystic fibrosis during the first pandemic wave in Italy: a multi-centre prospective study with a control group

Journal of cystic fibrosis, 2021, Vol.20, p.S80-S80

2021

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Glucose tolerance changes in cystic fibrosis (CF) patients during a 10 years period

Journal of cystic fibrosis, 2008-06, Vol.7, p.S84-S84

2008

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Walking distance as an outcome of antibiotic course in patients with cystic fibrosis

Journal of cystic fibrosis, 2008-06, Vol.7, p.S60-S60

2008

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Achille Ardigò and the sociology of the territory

Studi di sociologia, 2010-04, Vol.48 (2), p.223-230

Pisi, G

2010

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P254 Ivacaftor treatment in patients with severe lung disease carrying CFTR mutations with residual function

Journal of cystic fibrosis, 2019-06, Vol.18, p.S128-S129

2019

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Three-dimensional quantitative assessment of lung parenchyma in cystic fibrosis: preliminary results

Radiologia medica, 2007-02, Vol.112 (1), p.21-30

2007

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P243 Anxiety and depression in adolescents and adults with cystic fibrosis

Thorax, 2011-12, Vol.66 (Suppl 4), p.A167-A167

2011

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Detection of Small Airway Dysfunction in Asymptomatic Smokers with Preserved Spirometry: The Value of the Impulse Oscillometry System

Relationship between quality of life and behavioural disorders in children with persistent asthma: a Multiple Indicators Multiple Causes (MIMIC) model

Effect of elexacaftor–tezacaftor–ivacaftor modulator on lung structure in cystic fibrosis

63 Respiratory infections in children with cystic fibrosis (CF). Relationship with clinical and functional features

Insulin production and resistance in cystic fibrosis: Effect of age, disease activity, and genotype

203 Low dose azithromycin may slow the decline of respiratory function in cystic fibrosis

P065 Use of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with rare mutations

P156 Effects of lumacaftor/ivacaftor in CF children 2–6 years old: a case series

WS6.9 Cystic fibrosis related diabetes (CFRD): evidence for a role of miR-155, miR-370 and miR-708

P187 Small airways disease in cystic fibrosis patients

P134 Prevalence of multi-drug, antimicrobial-resistant bacteria in children with cystic fibrosis

Six-minute walking test in cystic fibrosis adults with mild to moderate lung disease: comparison to healthy subjects

P131 Clinical impact of Aspergillus fumigatus in children with cystic fibrosis

NUTRITIONAL AND RESPIRATORY EFFECTS OF AZITHROMYCIN LONG-TERM TREATMENT IN CYSTIC FIBROSIS PATIENTS

ePS4.07 COVID-19 early vaccination campaign in Italian cystic fibrosis (CF) patients: the experience of the Italian Society for the Study of Cystic Fibrosis (SIFC)

IPD2.05 Effects of ivacaftor in patients with cystic fibrosis and severe lung disease carrying CFTR mutations with residual function

WS13.6 Urinary incontinence in adult patients with cystic fibrosis: prevalence, impact on daily life and relationship with chronic cough

P157 Role of osteopathic manipulative treatment in cystic fibrosis: a pilot study

P134 SARS-CoV-2 infection in cystic fibrosis during the first pandemic wave in Italy: a multi-centre prospective study with a control group

Glucose tolerance changes in cystic fibrosis (CF) patients during a 10 years period

Walking distance as an outcome of antibiotic course in patients with cystic fibrosis

Achille Ardigò and the sociology of the territory

P254 Ivacaftor treatment in patients with severe lung disease carrying CFTR mutations with residual function

Three-dimensional quantitative assessment of lung parenchyma in cystic fibrosis: preliminary results

P243 Anxiety and depression in adolescents and adults with cystic fibrosis

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