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Genetic and clinical variations in a Norwegian sample diagnosed with Rett syndrome.
Henriksen, Mari Wold; Breck, Hilde; Sejersted, Yngve; Diseth, Trond; von Tetzchner, Stephen; Paus, Benedicte; Skjeldal, Ola H.
Afiliación
  • Henriksen MW; Department of Neurology, Drammen Hospital, Vestre Viken Hospital Trust, P.O. Box 800, 3004 Drammen, Norway; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, P.O. Box 1171, Blindern 0318, Oslo, Norway. Electronic address: mari.wold.henriksen@vestreviken.no.
  • Breck H; Department of Habilitation, Innlandet Hospital Trust, Anders Sandvigs v. 17, 2629 Lillehammer, Norway; Department of Psychology, University of Oslo, P.O. Box 1094, Blindern 0317, Oslo, Norway.
  • Sejersted Y; Department of Medical Genetics, Oslo University Hospital, Box 4950, 0424 Oslo, Norway.
  • Diseth T; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, P.O. Box 1171, Blindern 0318, Oslo, Norway.
  • von Tetzchner S; Department of Psychology, University of Oslo, P.O. Box 1094, Blindern 0317, Oslo, Norway.
  • Paus B; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, P.O. Box 1171, Blindern 0318, Oslo, Norway; Department of Medical Genetics, Oslo University Hospital, Box 4950, 0424 Oslo, Norway.
  • Skjeldal OH; Gillberg Neuropsychiatry Centre, Sahlgrenska Academy, University of Gothenburg, Kungsgatan 12, 41119 Gothenburg, Sweden.
Brain Dev ; 42(7): 484-495, 2020 Aug.
Article en En | MEDLINE | ID: mdl-32336485
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Rett / Sistema de Registros / Epilepsia / Proteína 2 de Unión a Metil-CpG Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Middle aged País/Región como asunto: Europa Idioma: En Revista: Brain Dev Año: 2020 Tipo del documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Rett / Sistema de Registros / Epilepsia / Proteína 2 de Unión a Metil-CpG Tipo de estudio: Diagnostic_studies / Etiology_studies / Prognostic_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Middle aged País/Región como asunto: Europa Idioma: En Revista: Brain Dev Año: 2020 Tipo del documento: Article