Claude Cancés

De novo mutations in HCN1 cause early infantile epileptic encephalopathy

Caroline Nava, Carine Dalle, Agnès Rastetter et al. · Nature Genetics · 2014 · 230 citations · Full text

Genetic Disorder, Genetics, Neuroscience +4

Motor and respiratory heterogeneity in Duchenne patients: Implication for clinical trials

Véronique Humbertclaude, Dalil Hamroun, Kamel Bezzou et al. · European Journal of Paediatric Neurology · 2011 · 138 citations

Medicine, Respiratory Neurobiology, Physiology +11

A randomized placebo-controlled phase 3 trial of an antisense oligonucleotide, drisapersen, in Duchenne muscular dystrophy

Nathalie Goemans, Eugenio Mercuri, Hirofumi Komaki et al. · Neuromuscular Disorders · 2017 · 119 citations · Full text

Duchenne Muscular Dystrophy, Medicine, Clinical Trials +5

Nusinersen in patients older than 7 months with spinal muscular atrophy type 1

Karolina Aragon‐Gawinska, Andreea Seferian, Aurore Daron et al. · Neurology · 2018 · 117 citations

Natural history of Type 2 and 3 spinal muscular atrophy: 2‐year NatHis‐SMA study

M. Annoussamy, A. Seferian, Aurore Daron et al. · Annals of Clinical and Translational Neurology · 2020 · 109 citations · Full text