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Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features.
Blumkin, Lubov; Leibovitz, Zvi; Krajden-Haratz, Karina; Arad, Ayala; Yosovich, Keren; Gindes, Liat; Zerem, Ayelet; Ben-Sira, Liat; Lev, Dorit; Nissenkorn, Andrea; Kidron, Dvora; Dobyns, William B; Malinger, Gustavo; Bahi-Buisson, Nadia; Leventer, Richard J; Lerman-Sagie, Tally.
Afiliação
  • Blumkin L; Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel; Pediatric Neurology Unit, Wolfson Medical Center, Holon, Israel; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel. Electronic address: luba.blumkin@gmail.com.
  • Leibovitz Z; Fetal Neurology Clinic, Wolfson Medical Center, Holon, Israel; Obstetrics-Gynecology Ultrasound Unit, Bnai-Zion Medical Center and Rappaport Faculty of Medicine, The Technion, Haifa, Israel.
  • Krajden-Haratz K; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; OB-GYN Ultrasound Unit, Lis Maternity Hospital, Sourasky Tel Aviv Medical Center, Tel Aviv, Israel.
  • Arad A; Department of Pathology, Bnai Zion Medical Center and Rappaport Faculty of Medicine, The Technion, Haifa, Israel.
  • Yosovich K; Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel; Molecular Genetics Laboratory, Wolfson Medical Center, Holon, Israel.
  • Gindes L; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; Fetal Neurology Clinic, Wolfson Medical Center, Holon, Israel.
  • Zerem A; Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel; Pediatric Neurology Unit, Wolfson Medical Center, Holon, Israel; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Ben-Sira L; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; Pediatric Radiology Unit, Tel Aviv Medical Center, Tel-Aviv, Israel.
  • Lev D; Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel; Pediatric Neurology Unit, Wolfson Medical Center, Holon, Israel; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; The Rina Mor Institute of Medical Genetics, Wolfson Medical Center, Holon, Israel.
  • Nissenkorn A; Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel; Pediatric Neurology Unit, Wolfson Medical Center, Holon, Israel; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
  • Kidron D; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; Deaprtment of Pathology, Meir Medical Center, Kfar Saba, Israel.
  • Dobyns WB; Center for Integrative Brain Research, Seattle Children's Research Institute, Department of Pediatrics, University of Washington, Department of Neurology, University of Washington, Seattle, WA, USA.
  • Malinger G; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel; OB-GYN Ultrasound Unit, Lis Maternity Hospital, Sourasky Tel Aviv Medical Center, Tel Aviv, Israel.
  • Bahi-Buisson N; Department of Pediatric Neurology, Necker Enfants Malades University Hospital, Paris Descartes University, Paris, France; Genetic and Development of Cerebral Cortex, INSERM UMR-1163, Imagine Institute, Paris Descartes University, Paris, France.
  • Leventer RJ; Department of Neurology, Royal Children's Hospital, Murdoch Children's Research Institute and Unibversity of Melbourne, Department of Pediatrics, Melbourne, Australia.
  • Lerman-Sagie T; Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel; Pediatric Neurology Unit, Wolfson Medical Center, Holon, Israel; Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Eur J Paediatr Neurol ; 26: 46-60, 2020 May.
Article em En | MEDLINE | ID: mdl-32169460
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tubulina (Proteína) / Feto / Malformações do Sistema Nervoso Tipo de estudo: Prognostic_studies Limite: Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn / Pregnancy Idioma: En Revista: Eur J Paediatr Neurol Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2020 Tipo de documento: Article País de publicação: Reino Unido
Texto completo
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XML
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tubulina (Proteína) / Feto / Malformações do Sistema Nervoso Tipo de estudo: Prognostic_studies Limite: Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn / Pregnancy Idioma: En Revista: Eur J Paediatr Neurol Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2020 Tipo de documento: Article País de publicação: Reino Unido