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Familial Intracranial Hypertension in 2 Brothers With PTEN Mutation: Expansion of the Phenotypic Spectrum.
Hady-Cohen, Ronen; Maharshak, Idit; Michelson, Marina; Yosovich, Keren; Lev, Dorit; Constantini, Shlomi; Leiba, Hana; Lerman-Sagie, Tally; Blumkin, Lubov.
Afiliação
  • Hady-Cohen R; 1 Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel.
  • Maharshak I; 2 Pediatric Neurology Unit, Wolfson Medical Center, Holon, Israel.
  • Michelson M; 3 Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Yosovich K; 3 Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Lev D; 4 Neuro-Ophthalmology Clinic, Ophthalmology Department, Wolfson Medical Center, Holon, Israel.
  • Constantini S; 1 Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel.
  • Leiba H; 3 Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Lerman-Sagie T; 5 The Rina Mor Institute of Medical Genetics, Wolfson Medical Center, Holon, Israel.
  • Blumkin L; 1 Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel.
J Child Neurol ; 34(9): 506-510, 2019 08.
Article em En | MEDLINE | ID: mdl-31046523
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipertensão Intracraniana / PTEN Fosfo-Hidrolase / Megalencefalia / Mutação Limite: Child / Child, preschool / Humans / Male Idioma: En Revista: J Child Neurol Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hipertensão Intracraniana / PTEN Fosfo-Hidrolase / Megalencefalia / Mutação Limite: Child / Child, preschool / Humans / Male Idioma: En Revista: J Child Neurol Ano de publicação: 2019 Tipo de documento: Article