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Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndrome.
Balci, Tugce B; Davila, Jorge; Lewis, Denice; Boafo, Addo; Sell, Erick; Richer, Julie; Nikkel, Sarah M; Armour, Christine M; Tomiak, Eva; Lines, Matthew A; Sawyer, Sarah L.
Afiliação
  • Balci TB; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Davila J; Department of Medical Imaging, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Lewis D; Department of Psychiatry, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Boafo A; Department of Family Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Sell E; Department of Psychiatry, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Richer J; Division of Neurology, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Nikkel SM; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Armour CM; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Tomiak E; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
  • Lines MA; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Sawyer SL; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
Am J Med Genet B Neuropsychiatr Genet ; 177(1): 101-109, 2018 Jan.
Article em En | MEDLINE | ID: mdl-29152901

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Hamartoma Múltiplo / PTEN Fosfo-Hidrolase / Leucoencefalopatias Tipo de estudo: Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Assunto da revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Hamartoma Múltiplo / PTEN Fosfo-Hidrolase / Leucoencefalopatias Tipo de estudo: Risk_factors_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Assunto da revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá