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Optimum insufflation capacity and peak cough flow in neuromuscular disorders

Annals of the American Thoracic Society, 2014-12, Vol.11 (10), p.1560-1568

2014

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Mechanical insufflation/exsufflation improves vital capacity in neuromuscular disorders

Chronic respiratory disease, 2015-02, Vol.12 (1), p.31-35

2015

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Practical Recommendations for Diagnosis and Management of Respiratory Muscle Weakness in Late-Onset Pompe Disease

International journal of molecular sciences, 2016-10, Vol.17 (10), p.1735-1735

2016

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Health-Related and Motor Performance-Related Fitness and Physical Activity Among Youth With Cystic Fibrosis

Perceptual and motor skills, 2021-10, Vol.128 (5), p.2097-2116

2021

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Association between habitual physical activity (HPA) and sleep quality in patients with cystic fibrosis

Sleep & breathing, 2021-06, Vol.25 (2), p.609-615

2021

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An 8 week open-label interventional multicenter study to explore the lung clearance index as endpoint for clinical trials in cystic fibrosis patients ≥8 years of age, chronically infected with Pseudomonas aeruginosa

BMC pulmonary medicine, 2020-06, Vol.20 (1), p.167-167, Article 167

2020

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Multiplex PCR of bronchoalveolar lavage fluid in children enhances the rate of pathogen detection

BMC pulmonary medicine, 2019-07, Vol.19 (1), p.132-132, Article 132

2019

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Trainability of Health-Related and Motor Performance Fitness in Adults with Cystic Fibrosis within a 12-Month Partially Supervised Exercise Program

Pulmonary medicine, 2021, Vol.2021, p.5581812-9

2021

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Longitudinal changes in habitual physical activity in adult people with cystic fibrosis in the presence or absence of treatment with elexacaftor/tezacaftor/ivacaftor

Frontiers in sports and active living, 2024, Vol.6, p.1284878-1284878

2024

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Long-Term Follow-Up of Health-Related Quality of Life and Short-Term Intervention with CFTR Modulator Therapy in Adults with Cystic Fibrosis: Evaluation of Changes over Several Years with or without 33 Weeks of CFTR Modulator Therapy

Healthcare (Basel), 2023-10, Vol.11 (21), p.2873

2023

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Long-term follow-up of pediatric patients receiving total body irradiation before hematopoietic stem cell transplantation and post-transplant survival of >2 years

Pediatric blood & cancer, 2013-11, Vol.60 (11), p.1792-1797

2013

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Sequential Inhalational Tobramycin-Colistin-Combination in CF-Patients with Chronic P. Aeruginosa Colonization - an Observational Study

Cellular physiology and biochemistry, 2016-01, Vol.39 (3), p.1141-1151

2016

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117th ENMC Workshop: Ventilatory Support in Congenital Neuromuscular Disorders — Congenital Myopathies, Congenital Muscular Dystrophies, Congenital Myotonic Dystrophy and SMA (II) 4–6 April 2003, Naarden, The Netherlands

Neuromuscular disorders : NMD, 2004, Vol.14 (1), p.56-69

2004

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Bacteraemia and fungaemia in cystic fibrosis patients with febrile pulmonary exacerbation: a prospective observational study

BMC pulmonary medicine, 2017-06, Vol.17 (1), p.96-96, Article 96

2017

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IPPB-assisted coughing in neuromuscular disorders

Pediatric pulmonology, 2006-06, Vol.41 (6), p.551-557

2006

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Glomerular and Tubular Renal Function after Repeated Once-Daily Tobramycin Courses in Cystic Fibrosis Patients

Pulmonary Medicine, 2017-01, Vol.2017 (2017), p.1-6-002

2017

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Pompe disease: A neuromuscular disease with respiratory muscle involvement

Respiratory medicine, 2009-04, Vol.103 (4), p.477-484

2009

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Airway clearance techniques in neuromuscular disorders: A state of the art review

Respiratory medicine, 2018-03, Vol.136, p.98-110

2018

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Nasal Staphylococcus aureus Carriage Is Not a Risk Factor for Lower-Airway Infection in Young Cystic Fibrosis Patients

Journal of Clinical Microbiology, 2007-09, Vol.45 (9), p.2979-2984

2007

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The microbiome and secondary lung disease in neuromuscular patients: Is it time to change our clinical practice? – Reply

Respirology (Carlton, Vic.), 2017-07, Vol.22 (5), p.1036-1036

2017

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Longitudinal Evaluation of Physical Fitness in Adults with Cystic Fibrosis in the Era of CFTR-Modulating-Therapies

Research quarterly for exercise and sport, 2024-03, p.1-9

2024

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Chest physiotherapy can affect the lung clearance index in cystic fibrosis patients

Pediatric pulmonology, 2017-05, Vol.52 (5), p.625-631

2017

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Normal values for inspiratory muscle function in children

Physiological measurement, 2014-10, Vol.35 (10), p.1975-1981

2014

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The microbiome and secondary lung disease in neuromuscular patients: I s it time to change our clinical practice? – Reply

Respirology (Carlton, Vic.), 2017-07, Vol.22 (5), p.1036-1036

2017

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Impact of habitual physical activity and exercise capacity on quality of life in adolescents and adults with cystic fibrosis

Pediatric pulmonology, 2024-04, Vol.59 (4), p.949-963

2024

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Optimum insufflation capacity and peak cough flow in neuromuscular disorders

Mechanical insufflation/exsufflation improves vital capacity in neuromuscular disorders

Practical Recommendations for Diagnosis and Management of Respiratory Muscle Weakness in Late-Onset Pompe Disease

Health-Related and Motor Performance-Related Fitness and Physical Activity Among Youth With Cystic Fibrosis

Association between habitual physical activity (HPA) and sleep quality in patients with cystic fibrosis

An 8 week open-label interventional multicenter study to explore the lung clearance index as endpoint for clinical trials in cystic fibrosis patients ≥8 years of age, chronically infected with Pseudomonas aeruginosa

Multiplex PCR of bronchoalveolar lavage fluid in children enhances the rate of pathogen detection

Trainability of Health-Related and Motor Performance Fitness in Adults with Cystic Fibrosis within a 12-Month Partially Supervised Exercise Program

Longitudinal changes in habitual physical activity in adult people with cystic fibrosis in the presence or absence of treatment with elexacaftor/tezacaftor/ivacaftor

Long-Term Follow-Up of Health-Related Quality of Life and Short-Term Intervention with CFTR Modulator Therapy in Adults with Cystic Fibrosis: Evaluation of Changes over Several Years with or without 33 Weeks of CFTR Modulator Therapy

Long-term follow-up of pediatric patients receiving total body irradiation before hematopoietic stem cell transplantation and post-transplant survival of >2 years

Sequential Inhalational Tobramycin-Colistin-Combination in CF-Patients with Chronic P. Aeruginosa Colonization - an Observational Study

117th ENMC Workshop: Ventilatory Support in Congenital Neuromuscular Disorders — Congenital Myopathies, Congenital Muscular Dystrophies, Congenital Myotonic Dystrophy and SMA (II) 4–6 April 2003, Naarden, The Netherlands

Bacteraemia and fungaemia in cystic fibrosis patients with febrile pulmonary exacerbation: a prospective observational study

IPPB-assisted coughing in neuromuscular disorders

Glomerular and Tubular Renal Function after Repeated Once-Daily Tobramycin Courses in Cystic Fibrosis Patients

Pompe disease: A neuromuscular disease with respiratory muscle involvement

Airway clearance techniques in neuromuscular disorders: A state of the art review

Nasal Staphylococcus aureus Carriage Is Not a Risk Factor for Lower-Airway Infection in Young Cystic Fibrosis Patients

The microbiome and secondary lung disease in neuromuscular patients: Is it time to change our clinical practice? – Reply

Longitudinal Evaluation of Physical Fitness in Adults with Cystic Fibrosis in the Era of CFTR-Modulating-Therapies

Chest physiotherapy can affect the lung clearance index in cystic fibrosis patients

Normal values for inspiratory muscle function in children

The microbiome and secondary lung disease in neuromuscular patients: I s it time to change our clinical practice? – Reply

Impact of habitual physical activity and exercise capacity on quality of life in adolescents and adults with cystic fibrosis

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