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Familial aggregation of focal seizure semiology in the Epilepsy Phenome/Genome Project.
Tobochnik, Steven; Fahlstrom, Robyn; Shain, Catherine; Winawer, Melodie R.
Afiliação
  • Tobochnik S; From the Department of Neurology and G.H. Sergievsky Center (S.T., M.R.W.), Columbia University, New York, NY; Department of Neurology (R.F.), University of California, San Francisco; and Department of Neurology (C.S.), Boston Children's Hospital, MA.
  • Fahlstrom R; From the Department of Neurology and G.H. Sergievsky Center (S.T., M.R.W.), Columbia University, New York, NY; Department of Neurology (R.F.), University of California, San Francisco; and Department of Neurology (C.S.), Boston Children's Hospital, MA.
  • Shain C; From the Department of Neurology and G.H. Sergievsky Center (S.T., M.R.W.), Columbia University, New York, NY; Department of Neurology (R.F.), University of California, San Francisco; and Department of Neurology (C.S.), Boston Children's Hospital, MA.
  • Winawer MR; From the Department of Neurology and G.H. Sergievsky Center (S.T., M.R.W.), Columbia University, New York, NY; Department of Neurology (R.F.), University of California, San Francisco; and Department of Neurology (C.S.), Boston Children's Hospital, MA. mw211@columbia.edu.
Neurology ; 89(1): 22-28, 2017 Jul 04.
Article em En | MEDLINE | ID: mdl-28566546

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espasmos Infantis / Núcleo Familiar / Epilepsias Parciais / Malformações do Desenvolvimento Cortical / Síndrome de Lennox-Gastaut Idioma: En Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Marrocos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espasmos Infantis / Núcleo Familiar / Epilepsias Parciais / Malformações do Desenvolvimento Cortical / Síndrome de Lennox-Gastaut Idioma: En Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Marrocos