Phenotype-genotype links and respiratory profiles in congenital muscular dystrophy (CMD) Source: Annual Congress 2010 - From the acute to the chronic patient: how do we use noninvasive ventilation? Year: 2010
Relationship between the reduced ventilatory response to CO2 and the impairment of the lung function in myotonic dystrophy patients Source: Annual Congress 2011 - Obstructive sleep apnoea: clinical aspects I Year: 2011
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
The impact of treatment with steroids on lung function of children with Duchenne muscular dystrophy: experience from a single centre Source: Virtual Congress 2020 – Respiratory physiology and sleep: what is new? Year: 2020
Effect of rehabilitation exercise on the extremity function and lung function in patients with Duchenne‘s muscular dystrophy Source: Eur Respir J 2006; 28: Suppl. 50, 372s Year: 2006
Relationship between the respiratory function with motor functionality in Duchenne Mucular Dystrophy Source: Virtual Congress 2020 – A knowledge update on respiratory muscle function, assessment and training Year: 2020
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
Effects of respiratory muscle training on strength and heart rate variability in myotonic dystrophy patients Source: Annual Congress 2010 - Respiratory muscles and breathing: assessment and training Year: 2010
Evolution of respiratory function in Duchenne muscular dystrophy from childhood to adulthood Source: Eur Respir J, 51 (2) 1701418; 10.1183/13993003.01418-2017 Year: 2018
Postural lung function changes in patients with myotonic dystrophy: A study on 59 patients Source: Annual Congress 2010 - Lung morbidity on exposure to various agents 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
Home-based versus hospital monitoring of respiratory function changes in Duchenne muscular dystrophy (DMD) Source: International Congress 2018 – Management of chronic cough and respiratory muscle dysfunction Year: 2018
Evaluating the effect of long-term idebenone treatment on respiratory morbidity in patients with Duchenne muscular dystrophy (DMD) Source: International Congress 2019 – Rare and ultra-rare diseases and the lungs: updates and new perspectives Year: 2019
Quality of life in patients with respiratory impairment due to muscular dystrophy Source: Eur Respir J 2004; 24: Suppl. 48, 545s Year: 2004
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
The change of ventilation function in the patients of Duchenne muscular dystrophy under and beyond 12 years old and the effects of rehabilitation Source: Eur Respir J 2007; 30: Suppl. 51, 766s Year: 2007
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
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
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
Age of loss of walking ability in patients with Duchenne muscular dystrophy: A marker for the elective use of mechanical ventilation? Source: Annual Congress 2011 - Exercise tests and emerging outcomes: defining the impact of pulmonary rehabilitation Year: 2011