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Genotype-phenotype correlation in French patients with myelin protein zero gene-related inherited neuropathy.
Subréville, Marie; Bonello-Palot, Nathalie; Yahiaoui, Douniazed; Beloribi-Djefaflia, Sadia; Fernandes, Sara; Stojkovic, Tanya; Cassereau, Julien; Péréon, Yann; Echaniz-Laguna, Andoni; Violleau, Marie-Hélène; Soulages, Antoine; Louis, Sarah Léonard; Masingue, Marion; Magot, Armelle; Delmont, Emilien; Sacconi, Sabrina; Adams, David; Labeyrie, Céline; Genestet, Steeve; Noury, Jean-Baptiste; Chanson, Jean-Baptiste; Lévy, Nicolas; Juntas-Morales, Raul; Tard, Céline; Sole, Guilhem; Attarian, Shahram.
Afiliação
  • Subréville M; Reference Center for Neuromuscular Disorders and ALS, APHM, CHU La Timone, Marseille, France.
  • Bonello-Palot N; Marseille Medical Genetics, Aix-Marseille University-Inserm UMR 1251, Marseille, France.
  • Yahiaoui D; Reference Center for Neuromuscular Disorders and ALS, APHM, CHU La Timone, Marseille, France.
  • Beloribi-Djefaflia S; Reference Center for Neuromuscular Disorders and ALS, APHM, CHU La Timone, Marseille, France.
  • Fernandes S; CEReSS-Health Service Research and Quality of Life Center, Aix-Marseille University, Marseille, France.
  • Stojkovic T; Reference Center for Neuromuscular Diseases North/East/Ile de France, Hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
  • Cassereau J; Reference Center for Neuromuscular Disorders AOC and National Reference Center for Neurogenetic Diseases, Angers University Hospital, Angers, France.
  • Péréon Y; Department of Clinical Neurophysiology, Reference Center for NMD, CHU Nantes, Nantes, France.
  • Echaniz-Laguna A; Department of Neurology, APHP, CHU de Bicêtre, Le Kremlin-Bicêtre, France.
  • Violleau MH; French National Reference Center for Rare Neuropathies, Le Kremlin-Bicêtre, France.
  • Soulages A; Inserm U1195 and Paris-Sud University, Le Kremlin-Bicêtre, France.
  • Louis SL; Reference Center for Neuromuscular Disorders AOC, CHU de Bordeaux, Bordeaux, France.
  • Masingue M; Reference Center for Neuromuscular Disorders AOC, CHU de Bordeaux, Bordeaux, France.
  • Magot A; Reference Center for Neuromuscular Diseases North/East/Ile de France, Hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
  • Delmont E; Reference Center for Neuromuscular Diseases North/East/Ile de France, Hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
  • Sacconi S; Department of Clinical Neurophysiology, Reference Center for NMD, CHU Nantes, Nantes, France.
  • Adams D; Reference Center for Neuromuscular Disorders and ALS, APHM, CHU La Timone, Marseille, France.
  • Labeyrie C; Peripheral Nervous System Service, Muscle et SLA, Centre Hospitalier Universitaire de Nice, Université Côte d'Azur, Nice, France.
  • Genestet S; Department of Neurology, APHP, CHU de Bicêtre, Le Kremlin-Bicêtre, France.
  • Noury JB; Department of Neurology, APHP, CHU de Bicêtre, Le Kremlin-Bicêtre, France.
  • Chanson JB; Neurology Department, CHRU Cavale Blanche, Brest, France.
  • Lévy N; Neurology Department, CHRU Cavale Blanche, Brest, France.
  • Juntas-Morales R; Department of Neurology, Hôpital de Hautepierre, CHU de Strasbourg, Strasbourg, France.
  • Tard C; Marseille Medical Genetics, Aix-Marseille University-Inserm UMR 1251, Marseille, France.
  • Sole G; Reference Center for Neuromuscular Disorders AOC, Department of Neurology, CHU Montpellier, Montpellier, France.
  • Attarian S; Inserm U1171, Department of Neurology, Reference Center for Neuromuscular Diseases North/East/Ile de France, CHU Lille, Lille University, Lille, France.
Eur J Neurol ; 28(9): 2913-2921, 2021 09.
Article em En | MEDLINE | ID: mdl-34060176
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Proteína P0 da Mielina Tipo de estudo: Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Proteína P0 da Mielina Tipo de estudo: Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article