C. Guillou

Early Treatment to Preserve Quality of Locomotion for Children with Duchenne Muscular Dystrophy

J. Bach, Y. Rideau, G. Duport, 1995, Seminars in neurology.

Genotype-phenotype correlations in Charcot-Marie-Tooth disease type 2 caused by mitofusin 2 mutations.

A. Toutain, B. Gilbert-Dussardier, P. Bouche, 2009, Archives of neurology.

Hypoosmotic shocks induce elevation of resting calcium level in duchenne muscular dystrophy myotubes contracting in vitro

C. Cognard, B. Constantin, G. Raymond, 1996, Neuromuscular Disorders.

Abnormal calcium homeostasis in Duchenne muscular dystrophy myotubes contracting in vitro.

C. Cognard, G. Raymond, G. Duport, 1995, Cell calcium.

[Early respiratory assistance by nasal route in Duchenne's muscular dystrophy].

Y. Rideau, A. Delaubier, C. Guillou, 1987, Agressologie: revue internationale de physio-biologie et de pharmacologie appliquees aux effets de l'agression.

Clinical implications of maximal respiratory pressure determinations for individuals with Duchenne muscular dystrophy.

J. Bach, J. Bach, A Hahn, 1997, Archives of physical medicine and rehabilitation.

Misconceptions about nasal ventilation

S. Chevret, C. Chastang, J. Bach, 1994, The Lancet.

Apical left ventricular myocardial dysfunction is an early feature of cardiac involvement in myotonic dystrophy type 1

P. Ingrand, L. Christiaens, B. Gellen, 2017, Echocardiography.

Treatment of respiratory insufficiency in Duchenne's muscular dystrophy: nasal ventilation in the initial stages.

Y. Rideau, A. Delaubier, C. Guillou, 1995, Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace.

Genotype-phenotype correlations in Charcot-Marie-Tooth disease type 2 caused by mitofusin 2 mutations.

A. Toutain, B. Gilbert-Dussardier, P. Bouche, 2009, Archives of neurology.