Clotilde Rivier

High frequency of creatine deficiency syndromes in patients with unexplained mental retardation

Laurence Lion‐François, David Cheillan, G. Pitelet et al. · Neurology · 2006 · 100 citations

Identification of an RNA-protein complex involved in chloroplast group II intron trans-splicing in Chlamydomonas reinhardtii

Clotilde Rivier · The EMBO Journal · 2001 · 91 citations · Full text

Biology, Rna Processing, Plant Molecular Biology +12

Molecular characterization of a cohort of 73 patients with infantile spasms syndrome

Nadia Boutry‐Kryza, Audrey Labalme, Dorothée Ville et al. · European Journal of Medical Genetics · 2014 · 71 citations

Molecular Characterization, Neurological Disorder, Pediatrics +5

An <scp><i>SCN2A</i></scp> mutation in a family with infantile seizures from Madagascar reveals an increased subthreshold <scp>N</scp>a⁺ current

Stephan Lauxmann, Nadia Boutry‐Kryza, Clotilde Rivier et al. · Epilepsia · 2013 · 42 citations

Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations

Pauline Marzin, Cyril Mignot, Nathalie Dorison et al. · Brain and Development · 2018 · 25 citations

Neurological Disorder, Genetic Disorder, Inherited Metabolic Disease +9