Assessment of NuvoAir platform use on clinical outcomes in adults with cystic fibrosis: a first Italian experience Source: Virtual Congress 2021 – Cystic fibrosis Year: 2021
From registry to quality management: the German Cystic Fibrosis Quality Assessment project 1995 2006 Source: Eur Respir J 2008; 31: 29-35 Year: 2008
A new paradigm for the management of children with cystic fibrosis at home: experiences from a Dutch cystic fibrosis clinic Source: Virtual Congress 2021 – New technologies for the management of children with respiratory diseases Year: 2021
Association of clinical variables in children with cystic fibrosis and health-related quality of life Source: Eur Respir J 2002; 20: Suppl. 38, 342s Year: 2002
Do causes influence clinical, functional and quality of life aspects on patients with bronchiectasis not associated with cystic fibrosis? Source: International Congress 2019 – Chronic cough, a1-antitrypsin deficiency and other conditions Year: 2019
Case study in cystic fibrosis: the US CF Foundation research and clinical development programmes Source: Research Seminar 2014 - Breaking down barriers to lung health: a better environment for better medicines Year: 2014
Quality of life and health utility in patients with cystic fibrosis Source: Annual Congress 2010 - Cystic fibrosis: clinical and laboratory studies Year: 2010
Age at diagnosis and follow up, standards of care in cystic fibrosis patients: impact on outcomes Source: Eur Respir J 2007; 30: Suppl. 51, 386s Year: 2007
Nurse-provided education improves adherence and quality of life in adult patients with cystic fibrosis Source: Virtual Congress 2020 – Challenges and updates in nursing care around the world Year: 2020
Comparative study of three quality of life instruments in adolescent and adults with cystic fibrosis Source: Annual Congress 2012 - Cystic fibrosis (adults and children): new aspects of risk factors, treatments and diagnosis Year: 2012
Home care and benefit in days of hospitalization, cost and quality of life for children with cystic fibrosis Source: International Congress 2016 – Kaleidoscope of respiratory nursing Year: 2016
Patient centred research: a model for involving cystic fibrosis (CF) patients in research planning Source: International Congress 2019 – Treatments, adherence and psychosocial aspects of cystic fibrosis Year: 2019
Optimising treatment policies and improvement of care: impact on outcome in cystic fibrosis patients Source: Eur Respir J 2004; 24: Suppl. 48, 617s Year: 2004
Hospital admissions are linked to a poor health related quality of life in patients with non cystic fibrosis bronchiectasis Source: Annual Congress 2007 - Pulmonary infections in the immunocompetent and immunocompromised host Year: 2007
Quality of life of paediatric patients with cystic fibrosis and their caregivers Source: Annual Congress 2011 - Cystic fibrosis: new basic, clinical and bacteriological knowledge Year: 2011
Management of patients with idiopathic pulmonary fibrosis in clinical practice: the INSIGHTS-IPF registry Source: Eur Respir J 2015; 46: 186-196 Year: 2015
Using registries to improve cystic fibrosis care Source: Eur Respir Monogr 2014; 64: 262-271 Year: 2014
Public awareness on cystic fibrosis: results from a national pragmatic survey Source: Eur Respir J 2015; 46: 264-267 Year: 2015