M. Chevallay

Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two families

Antonella Pini, Luciano Merlini, F. Tomé et al. · Brain and Development · 1996 · 63 citations

Periodic Spasms, Medicine, Motor Disorder +5

Immunocytochemical analysis of myosin heavy chains in human fetal skeletal muscles

F. Pons, Jocelyne Léger, M. Chevallay et al. · Journal of the Neurological Sciences · 1986 · 57 citations

Muscle Function, Molecular Physiology, Engineering +12

Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers

Jean‐François Marini, Françoise Pons, Jocelyne Léger et al. · Neuromuscular Disorders · 1991 · 52 citations

Muscle Function, Molecular Physiology, Skeletal Muscle +6

Congenital muscular dystrophy with primary partial laminin α2 chain deficiency: Molecular study

Yi He, Kristi Jones, Nicolas Vignier et al. · Neurology · 2001 · 52 citations

Rare Diseases, Mendelian Disorder, Skeletal Muscle +11

Late-onset rod myopathy associated with monoclonal gammopathy

B. Eymard, J C Brouet, H. Barry Collin et al. · Neuromuscular Disorders · 1993 · 47 citations

Late-onset Rod Myopathy, Pathology, Connective Tissue Disease