Rémi Valter

A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies

Marie Coutelier, Giulia Coarelli, Marie‐Lorraine Monin et al. · Brain · 2017 · 111 citations · Full text

Neurogenomics, Neurological Disorder, Genetics +23

Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia

Jean‐Loup Méreaux, Guillaume Banneau, Mélanie Papin et al. · Brain · 2021 · 63 citations · Full text

Index Patients, Pain Medicine, Genetics +25

A Protocol for the Use of Case Reports/Studies and Case Series in Systematic Reviews for Clinical Toxicology

Aboubakari Nambiema, Grace Sembajwe, Juleen Lam et al. · Frontiers in Medicine · 2021 · 51 citations · Full text

<i>NPTX1</i> mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia

Marie Coutelier, Maxime Jacoupy, Alexandre Janer et al. · Brain · 2021 · 27 citations · Full text

Exome Sequencing, Genetics, Disease Gene Identification +16

Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations

Jean‐Loup Méreaux, Cristina Firanescu, Giulia Coarelli et al. · Neurogenetics · 2021 · 15 citations · Full text