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Static Leukoencephalopathy Associated with 17p13.3 Microdeletion Syndrome: A Case Report.
Hirasawa-Inoue, Ayaka; Takeshita, Eri; Shimizu-Motohashi, Yuko; Ishiyama, Akihiko; Saito, Takashi; Komaki, Hirofumi; Nakagawa, Eiji; Sugai, Kenji; Inoue, Ken; Goto, Yu-Ichi; Sasaki, Masayuki.
Afiliación
  • Hirasawa-Inoue A; Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
  • Takeshita E; Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
  • Shimizu-Motohashi Y; Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
  • Ishiyama A; Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
  • Saito T; Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
  • Komaki H; Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
  • Nakagawa E; Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
  • Sugai K; Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
  • Inoue K; Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
  • Goto YI; Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
  • Sasaki M; Medical Genome Center, National Center of Neurology and Psychiatry (NCNP), Tokyo, Japan.
Neuropediatrics ; 50(6): 387-390, 2019 12.
Article en En | MEDLINE | ID: mdl-31370080
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 17 / Deleción Cromosómica / Leucoencefalopatías Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans Idioma: En Revista: Neuropediatrics Año: 2019 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Alemania
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 17 / Deleción Cromosómica / Leucoencefalopatías Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans Idioma: En Revista: Neuropediatrics Año: 2019 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Alemania