Louis Viollet

Medicine · Health Sciences

24h-index6.1kcitations60works0.02yr avg
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Research Topics

Neurogenetic and Muscular Disorders Research(34), RNA modifications and cancer(15), Muscle Physiology and Disorders(12), RNA Research and Splicing(8), Cardiomyopathy and Myosin Studies(6)

Publications60 total

Distal hereditary motor neuropathy with HSJ1 chaperone mutation presenting with movement disorders
Arquivos de Neuro-Psiquiatria·2024Open Access
TANGO: a placebo-controlled randomized phase 2 study of efficacy and safety of the anti-tau monoclonal antibody gosuranemab in early Alzheimer’s disease
Nature Aging·2023· 69 citedOpen Access
Baseline characteristics from TANGO: Phase 2 study to evaluate gosuranemab (BIIB092) in patients with early Alzheimer’s disease
Alzheimer s & Dementia·2020· 4 citedOpen Access
A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomalies
European Journal of Medical Genetics·2020· 7 citedOpen Access
Research conference summary from the 2014 International Task Force on <i>ATP1A3</i> -Related Disorders
Neurology Genetics·2017· 65 citedOpen Access
Research conference summary from the 2014 International Task Force on
Neurology Genetics·2017Open Access
Orthopedic Management of Scoliosis by Garches Brace and Spinal Fusion in SMA Type 2 Children
Journal of Neuromuscular Diseases·2015· 27 citedOpen Access
Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
PLoS ONE·2015· 12 citedOpen Access
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
PLoS ONE·2015· 74 citedOpen Access
Resistance strength training exercise in children with spinal muscular atrophy
Muscle & Nerve·2015· 102 citedOpen Access
Familial Episodic Encephalopathy, Dysarthria, and Paralysis Is Associated with a Dominantly Inherited Mutation in ATP1A3 (P4.335)
Neurology·2014
Spinal muscular atrophies
Handbook of clinical neurology·2013· 8 cited
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
Nature Genetics·2012· 417 citedOpen Access
Study of <i>LPIN1</i>, <i>LPIN2</i> and <i>LPIN3</i> in rhabdomyolysis and exercise‐induced myalgia
Journal of Inherited Metabolic Disease·2012· 89 citedOpen Access
A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation
Annals of Neurology·2011· 71 cited
P2.4 Searching for pulmonary outcome measures in ’Early Onset’ COL6-related myopathy
Neuromuscular Disorders·2011· 2 cited
P5.62 Garches muscle Whole-Body MRI protocol: Pattern recognition in early onset neuromuscular disorders
Neuromuscular Disorders·2011
Phenotype, Genetics and Natural History in 146 Patients with SEPN1-Related Myopathy: On the Way to Therapeutic Trials in a Rare Disorder
UCL Discovery (University College London)·2011
Riluzole pharmacokinetics in young patients with spinal muscular atrophy
British Journal of Clinical Pharmacology·2010· 24 citedOpen Access
Early onset collagen VI myopathies: Genetic and clinical correlations
Annals of Neurology·2010· 132 citedOpen Access
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Frequent Co-authors

B. Estournet(16), Pascale Guicheney(11), Pascale Richard(10), Norma B. Romero(10), Arnold Münnich(9), A Barois(9), Ana Ferreiro(8), Judith Melki(7), Kathryn J. Swoboda(7), Valérie Allamand(7), Susana Quijano‐Roy(6), Isabelle Maystadt(6), Olivier Clermont(5), Tara Newcomb(5), Suzie Lefebvre(5), Laura Briñas(5), Corine Gartioux(5), M. Mayer(5), Francis Renault(5), D. Leclair-Richard(5)