Neuromuscular disease Source: ISSN=1025-448x, ISBN=1-904097-17-0, page=218 Year: 2001
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
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
Abdominal volume contribution to tidal volume as an early indicator of respiratory impairment in Duchenne muscular dystrophy Source: Eur Respir J 2010; 35: 1118-1125 Year: 2010
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
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
Chest wall kinematics during cough in Duchenne muscular dystrophy (DMD) Source: Annual Congress 2010 - Functional assessment of paediatric lung disease Year: 2010
Effects of posture on peak cough flow and respiratory muscle activation in Duchenne muscular dystrophy Source: International Congress 2018 – New insights in testing lung and respiratory muscle functions Year: 2018
Pulmonary function in Duchenne muscular dystrophy patients before and after noninvasive ventilation Source: Eur Respir J 2005; 26: Suppl. 49, 85s Year: 2005
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
Inefficient cough in Duchenne muscular dystrophy (DMD) 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
Respiratory kinematics in Duchenne muscular dystrophy (DMD) Source: Eur Respir J 2007; 30: Suppl. 51, 376s Year: 2007
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
Respiratory function and sleep respiratory disorders in facio-scapulo-humeral dystrophy (FSHD) Source: Annual Congress 2008 - Weight control and comorbidity in obstructive sleep apnoea Year: 2008
Noninvasive ventilation for chest wall and neuromuscular disorders Source: Eur Respir J 2002; 20: 480-487 Year: 2002
Pathogenesis of daytime hypercapnia in myotonic dystrophy Source: Annual Congress 2010 - From the acute to the chronic patient: how do we use noninvasive ventilation? Year: 2010
Evolution of pulmonary function in children with Duchenne muscular dystrophy: implication of expiratory muscles Source: Eur Respir J 2005; 26: Suppl. 49, 499s Year: 2005
Inspiratory and expiratory muscle weakness in facioscapulohumeral muscular dystrophy Source: International Congress 2019 – Lung function and respiratory muscle testing Year: 2019