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Dysregulation of NEUROG2 plays a key role in focal cortical dysplasia.
Avansini, Simoni H; Torres, Fábio R; Vieira, André S; Dogini, Danyella B; Rogerio, Fabio; Coan, Ana C; Morita, Marcia E; Guerreiro, Marilisa M; Yasuda, Clarissa L; Secolin, Rodrigo; Carvalho, Benilton S; Borges, Murilo G; Almeida, Vanessa S; Araújo, Patrícia A O R; Queiroz, Luciano; Cendes, Fernando; Lopes-Cendes, Iscia.
Afiliação
  • Avansini SH; Department of Medical Genetics, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Torres FR; Department of Medical Genetics, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Vieira AS; Department of Medical Genetics, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Dogini DB; Department of Medical Genetics, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Rogerio F; Department of Anatomical Pathology, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Coan AC; Department of Neurology, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Morita ME; Department of Neurology, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Guerreiro MM; Department of Neurology, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Yasuda CL; Department of Neurology, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Secolin R; Department of Medical Genetics, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Carvalho BS; Department of Medical Genetics, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Borges MG; Department of Medical Genetics, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Almeida VS; Department of Medical Genetics, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Araújo PAOR; Department of Medical Genetics, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Queiroz L; Department of Anatomical Pathology, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Cendes F; Department of Neurology, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
  • Lopes-Cendes I; Department of Medical Genetics, University of Campinas and Brazilian Institute of Neuroscience and Neurotechnology, Campinas, Brazil.
Ann Neurol ; 83(3): 623-635, 2018 03.
Article em En | MEDLINE | ID: mdl-29461643
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipoplasia Dérmica Focal / Epilepsia / Fatores de Transcrição Hélice-Alça-Hélice Básicos / Malformações do Desenvolvimento Cortical / Proteínas do Tecido Nervoso Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Ann Neurol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Brasil País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipoplasia Dérmica Focal / Epilepsia / Fatores de Transcrição Hélice-Alça-Hélice Básicos / Malformações do Desenvolvimento Cortical / Proteínas do Tecido Nervoso Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Ann Neurol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Brasil País de publicação: Estados Unidos