B. Eymard

Cold extends electromyography distinction between ion channel mutations causing myotonia

Emmanuel Fournier, Karine Viala, Hélène Gervais et al. · Annals of Neurology · 2006 · 157 citations

Medicine, Genetics, Neurology +15

Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget’s disease of bone and frontotemporal dementia

Tanya Stojkovic, El Hadi Hammouda, Pascale Richard et al. · Neuromuscular Disorders · 2009 · 84 citations

Medicine, Neurology, Neuroscience +12

Exercise-induced muscle modifications: study of healthy subjects and patients with metabolic myopathies with MR imaging and P-31 spectroscopy.

É. de Kerviler, Anne Leroy‐Willig, P. Jehenson et al. · Radiology · 1991 · 71 citations

Life Sciences, Biochemistry, Physiology +17

Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age

Sandra Mercier, Annick Toutain, Aurélie Toussaint et al. · European Journal of Human Genetics · 2013 · 68 citations · Full text

Medicine, Child Health, Pediatrics +8

Phenotypic spectrum and incidence of <i>TRPV4</i> mutations in patients with inherited axonal neuropathy

Andoni Echaniz‐Laguna, O. Dubourg, Pierre G. Carlier et al. · Neurology · 2014 · 66 citations · Full text

Life Sciences, Genetics, Neurology +17