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Long-term benefit of enzyme replacement therapy with alglucosidase alfa in adults with Pompe disease: prospective analysis from the French Pompe Registry
Semplicini C, De Antonio M, Taouagh N, et al.
Journal of inherited metabolic disease, 2020
Factors associated with the type of mask used during nocturnal NIV in patients with neuromuscular disorders
Leotard A, Lebret M, Prigent H, et al.
Revue des maladies respiratoires, 2020, 37, 2, p 99
Respiratory muscle dysfunction in facioscapulohumeral muscular dystrophy. Reference article: Sleep-related breathing disorders in facioscapulohumeral dystrophy
Santos DR, Boussaïd G, Stojkovic T, et al.
Sleep and Breathing, 2019
Peak Cough Flow Fails to Detect Upper Airway Collapse During Negative Pressure Titration for Cough-Assist
Lacombe M, Bore A, Amo Castrillo LD, et al.
Archives of physical medicine and rehabilitation, 2019
Diaphragm sniff ultrasound: Normal values, relationship with sniff nasal pressure and accuracy for predicting respiratory involvement in patients with neuromuscular disorders
Fayssoil A, Nguyen LS, Ogna A, et al.
PLoS ONE, 2019, 14, 4
Quel suivi pour les traitements innovants ?
Campana-Salort E, Espil-Taris C, Prigent H, et al.
médecine/sciences, 2019, 35, HS1, p 54
Echographic Assessment of Diaphragmatic Function in Duchenne Muscular Dystrophy from Childhood to Adulthood
Fayssoil A, Chaffaut C, Ogna A, et al.
Journal of Neuromuscular Diseases, 2019, 6, 1, p 55
Assessment of diaphragm motion using ultrasonography in a patient with facio-scapulo-humeral dystrophy: A case report
Fayssoil A, Fayssoil A, Stojkovic T, et al.
Medicine, 2019, 98, 4
Flow and airway pressure analysis for detecting ineffective effort during mechanical ventilation in neuromuscular patients
Ciorba C, Gonzalez-Bermejo J, Salva MQ, et al.
Chronic respiratory disease, 2018, 16
Mechanical Insufflation-Exsufflation to Improve Secretion Clearance During Invasive Ventilation.
Terzi N, Prigent H, Lofaso F
Respiratory care, 2018, 63, 12, p. 1577-1578
Effects of Home Mechanical Ventilation on Left Ventricular Function in Sarcoglycanopathies (Limb Girdle Muscular Dystrophies)
Fayssoil A, Nguyen LS, Ogna A, et al.
The American journal of cardiology, 2018
Effect and impact of mechanical ventilation in myotonic dystrophy type 1: a prospective cohort study
Boussaïd G, Prigent H, Laforêt P, et al.
Thorax, 2018
Genotype and other determinants of respiratory function in myotonic dystrophy type 1
Boussaïd G, Wahbi K, Laforêt P, et al.
Neuromuscular disorders : NMD, 2018, 28, 3, p 222
Natural history of cardiac function in Duchenne and Becker muscular dystrophies on home mechanical ventilation
Fayssoil A, Ogna A, Chaffaut C, et al.
Medicine, 2018, 97, 27
Non invasive mechanical ventilation in DM1: The strong correlation between lung function, neurological-cognitive function and CTG repeats
Lofaso F, Prigent H, Annane D, et al.
Neuromuscular disorders : NMD, 2018, 28, 10, p 894
Non-invasive mechanical ventilation in myotonic dystrophy type 1? Hypoventilation versus quality of life perspective
Boussaïd G, Lofaso F, Orlikowski D, et al.
Neuromuscular disorders : NMD, 2018, 28, 2, p 194
Left bundle branch block in Duchenne muscular dystrophy: Prevalence, genetic relationship and prognosis
Fayssoil A, Ben Yaou R, Ogna A, et al.
PLoS ONE, 2018, 13, 1
Bench evaluation of commercially available and newly developed interfaces for mouthpiece ventilation
Ogna A, Prigent H, Falaize L, et al.
The clinical respiratory journal, 2018, 12, 3, p 890
Diaphragm: Pathophysiology and Ultrasound Imaging in Neuromuscular Disorders
Fayssoil A, Behin A, Ogna A, et al.
Journal of Neuromuscular Diseases, 2017
Short-term effect of volume recruitment-derecruitment manoeuvre on chest-wall motion in Duchenne muscular dystrophy
Meric H, Falaize L, Pradon D, et al.
Chronic respiratory disease, 2017, 14, 2, p 110
Outcomes of Hospitalised Muscular Dystrophy Patients
Boussaïd G, Prigent H, Caranhac G, et al.
Journal of Neuromuscular Diseases, 2017, 4, 2, p 165
Effect of enzyme replacement therapy with alglucosidase alfa (Myozyme®) in 12 patients with advanced late-onset Pompe disease
Papadopoulos C, Orlikowski D, Prigent H, et al.
Molecular genetics and metabolism, 2017, 122, 1-2, p 80
Twitch mouth pressure for detecting respiratory muscle weakness in suspicion of neuromuscular disorder
Santos DB, Desmarais G, Falaize L, et al.
Neuromuscular disorders : NMD, 2017, 27, 6, p 518
Assisted vital capacity to assess recruitment level in neuromuscular diseases
Santos DB, Bore A, Castrillo LDA, et al.
Respiratory physiology & neurobiology, 2017, 243, p 32
Home monitoring of daytime mouthpiece ventilation effectiveness in patients with neuromuscular disease.
Nardi J, Leroux K, Orlikowski D, et al.
Chronic respiratory disease, 2016, 13, 1, p.67-74
