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The LORIS MyeliNeuroGene rare disease database for natural history studies and clinical trial readiness.
Spahr, Aaron; Rosli, Zaliqa; Legault, Mélanie; Tran, Luan T; Fournier, Simon; Toutounchi, Helia; Darbelli, Lama; Madjar, Cécile; Lucia, Cassandra; St-Jean, Marie-Lou; Das, Samir; Evans, Alan C; Bernard, Geneviève.
Afiliação
  • Spahr A; Department of Neurology and Neurosurgery, McGill University, Montréal, Québec, Canada.
  • Rosli Z; Department of Pediatrics, McGill University, Montréal, Québec, Canada.
  • Legault M; Department of Human Genetics, McGill University, Montréal, Québec, Canada.
  • Tran LT; Department of Specialized Medicine, Division of Medical Genetics, McGill University Health Centre, Montréal, Québec, Canada.
  • Fournier S; Child Health and Human Development Program, Research Institute, McGill University Health Center, Montréal, Québec, Canada.
  • Toutounchi H; McGill Centre for Integrative Neuroscience, Montreal Neurological Institute, McGill University, Montréal, Québec, Canada.
  • Darbelli L; McGill Centre for Integrative Neuroscience, Montreal Neurological Institute, McGill University, Montréal, Québec, Canada.
  • Madjar C; Department of Neurology and Neurosurgery, McGill University, Montréal, Québec, Canada.
  • Lucia C; Department of Pediatrics, McGill University, Montréal, Québec, Canada.
  • St-Jean ML; Department of Human Genetics, McGill University, Montréal, Québec, Canada.
  • Das S; Department of Specialized Medicine, Division of Medical Genetics, McGill University Health Centre, Montréal, Québec, Canada.
  • Evans AC; Child Health and Human Development Program, Research Institute, McGill University Health Center, Montréal, Québec, Canada.
  • Bernard G; Department of Neurology and Neurosurgery, McGill University, Montréal, Québec, Canada.
Orphanet J Rare Dis ; 16(1): 328, 2021 07 23.
Article em En | MEDLINE | ID: mdl-34301277
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Doenças Raras Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Female / Humans / Pregnancy País/Região como assunto: America do norte Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Canadá
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Doenças Raras Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Female / Humans / Pregnancy País/Região como assunto: America do norte Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Canadá