NIV and neuromuscular disease Source: Eur Respir Mon; 2008: 41: 224–239 Year: 2008
Sleep in patients with Duchenne muscular dystrophy (DMD) and spinal muscular atrophy (SMA): is there a difference? Source: Eur Respir J 2001; 18: Suppl. 33, 88s Year: 2001
Pulmonary function in Duchenne muscular dystrophy patients before and after noninvasive ventilation Source: Eur Respir J 2005; 26: Suppl. 49, 85s Year: 2005
Home monitoring and starting non-invasive ventilation in patients with neuromuscular disorders including amyotrophic lateral sclerosis Source: Sleep and Breathing Conference 2021 Year: 2021
The lung function disturbances in patients with muscular dystrophies, Charcot-Marie-Tooth‘s disease, myasthenia gravis and spinal muscular atrophy Source: Eur Respir J 2006; 28: Suppl. 50, 861s Year: 2006
Implication of regular pulmonary function evaluation in Duchenne muscular dystrophy Source: Virtual Congress 2020 – Pulmonary function and rehabilitation in non-respiratory disease Year: 2020
Human diaphragm atrophy in amyotrophic lateral sclerosis is not predicted by routine respiratory measures Source: Eur Respir J, 53 (2) 1801749; 10.1183/13993003.01749-2018 Year: 2019
Respiratory kinematics in Duchenne muscular dystrophy (DMD) Source: Eur Respir J 2007; 30: Suppl. 51, 376s Year: 2007
Thoraco-abdominal asynchronies during spontaneous breathing in Duchenne muscular dystrophy (DMD) Source: Annual Congress 2012 - Physiological monitoring during sleep and in neuromuscular disease in children Year: 2012
Gastrointestinal dysfunction in ventilated patients with Duchenne muscular dystrophy Source: Annual Congress 2012 - Current trends in home mechanical ventilation Year: 2012
Nutritional status and admission risk in Duchenne muscular dystrophy (DMD) Source: Annual Congress 2013 –Novel biomarkers and old parameters in clinical management of lung diseases Year: 2013
Which are the most informative parameters to follow the respiratory decline in Duchenne muscular dystrophy? Source: Annual Congress 2012 - Physiological monitoring during sleep and in neuromuscular disease in children Year: 2012
Ventilatory assistance in patients with Duchenne muscular dystrophy Source: Eur Respir J 2006; 28: 468-469 Year: 2006
Effects of idebenone on pulmonary morbidity in Duchenne muscular dystrophy (DMD) Source: International Congress 2017 – New ideas for the management of chronic lung diseases Year: 2017
Inspiratory muscle dysfunction relates to clinical disease severity in patients with type I myotonic dystrophy Source: International Congress 2019 – Lung function and respiratory muscle testing Year: 2019
Diaphragm dysfunction in patients with amylotrophic lateral sclerosis Source: International Congress 2017 – New frontiers in home care management of chronic lung diseases Year: 2017
Respiratory muscle testing: a valuable tool for young patients with Duchenne muscular dystrophy Source: Eur Respir J 2006; 28: Suppl. 50, 357s Year: 2006
Respiratory function, scoliosis and arthrodesis in Duchenne muscular dystrophy Source: International Congress 2015 – Respiratory physiology in children: technical and clinical aspects Year: 2015
Posterior spinal fusion for scoliosis in Duchenne muscular dystrophy diminishes the rate of respiratory decline Source: Eur Respir J 2003; 22: Suppl. 45, 309s Year: 2003
Assessment of diaphragm thickness variations by ultrasonography in patients with Duchenne muscular dystrophy (DMD) Source: Annual Congress 2012 - Physiological monitoring during sleep and in neuromuscular disease in children Year: 2012