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Epilepsy in KCNH1-related syndromes.
Mastrangelo, Mario; Scheffer, Ingrid E; Bramswig, Nuria C; Nair, Lal D V; Myers, Candace T; Dentici, Maria Lisa; Korenke, Georg C; Schoch, Kelly; Campeau, Philippe M; White, Susan M; Shashi, Vandana; Kansagra, Sujay; Van Essen, Anthonie J; Leuzzi, Vincenzo.
Afiliação
  • Mastrangelo M; Pediatric Neurology Division Department of Pediatrics, Child Neurology and Psychiatry, Sapienza-University of Rome, Rome, Italy.
  • Scheffer IE; Florey Institute and University of Melbourne, Austin Health and Royal Children's Hospital, Melbourne, Australia.
  • Bramswig NC; Institut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, Germany.
  • Nair LD; Department of Pediatrics, Saveetha Medical College, Chennai, India.
  • Myers CT; Department of Pediatrics, University of Washington, Seattle, WA, USA.
  • Dentici ML; Bambino Gesù Children Hospital, Rome, Italy.
  • Korenke GC; Klinik für Neuropädiatrie, Klinikum Oldenburg, Germany.
  • Schoch K; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, USA.
  • Campeau PM; Department of Pediatrics, University of Montreal, Montreal, Canada.
  • White SM; Victorian Clinical Genetics Services, Murdoch Childrens Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia, Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia.
  • Shashi V; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, USA.
  • Kansagra S; Division of Pediatric Neurology, Department of Pediatrics, Duke University Medical Center, Durham, USA.
  • Van Essen AJ; Department of Genetics, University of Groningen, University Medical Center Groningen, The Netherlands.
  • Leuzzi V; Pediatric Neurology Division Department of Pediatrics, Child Neurology and Psychiatry, Sapienza-University of Rome, Rome, Italy.
Epileptic Disord ; 18(2): 123-36, 2016 Jun 01.
Article em En | MEDLINE | ID: mdl-27267311
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polegar / Anormalidades Múltiplas / Deformidades Congênitas da Mão / Hallux / Anormalidades Craniofaciais / Epilepsia / Canais de Potássio Éter-A-Go-Go / Fibromatose Gengival / Deficiência Intelectual / Unhas Malformadas Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Epileptic Disord Assunto da revista: CEREBRO / NEUROLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Itália País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polegar / Anormalidades Múltiplas / Deformidades Congênitas da Mão / Hallux / Anormalidades Craniofaciais / Epilepsia / Canais de Potássio Éter-A-Go-Go / Fibromatose Gengival / Deficiência Intelectual / Unhas Malformadas Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Epileptic Disord Assunto da revista: CEREBRO / NEUROLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Itália País de publicação: Estados Unidos