Michel Fardeau

Macrophagic myofasciitis: an emerging entity

P. Laforêt, F. Authier, M. Fardeau, 1998, The Lancet.

Morphometric analysis of mdx diaphragm muscle fibres. Comparison with hindlimb muscles

M. Fardeau, J. Louboutin, E. Thaon, 1993, Neuromuscular Disorders.

Storage of phosphorylated desmin in a familial myopathy

C. Delcayre, M. Fardeau, F. Tomé, 1988, FEBS letters.

Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region.

A. Poustka, J. Mandel, W. Kress, 1996, Human molecular genetics.

Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region.

M. Fardeau, J. Gouyon, N. Dahl, 1995, American journal of human genetics.

Distinct contractile protein profile in congenital myotonic dystrophy and X-linked myotubular myopathy

G. Butler-Browne, C. Laurent‐Winter, M. Chevallay, 1991, Neuromuscular Disorders.

Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation.

C. Philippe, M. Fardeau, F. Tomé, 1994, American journal of medical genetics.

Glycogen-storage disease type II (acid maltase deficiency): identification of a novel small deletion (delCC482+483) in French patients.

A. Kahn, M. Fardeau, M. Nicolino, 1997, Biochemical and biophysical research communications.