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Phenotypic insights into ADCY5-associated disease.
Chang, Florence C F; Westenberger, Ana; Dale, Russell C; Smith, Martin; Pall, Hardev S; Perez-Dueñas, Belen; Grattan-Smith, Padraic; Ouvrier, Robert A; Mahant, Neil; Hanna, Bernadette C; Hunter, Matthew; Lawson, John A; Max, Christoph; Sachdev, Rani; Meyer, Esther; Crimmins, Dennis; Pryor, Donald; Morris, John G L; Münchau, Alex; Grozeva, Detelina; Carss, Keren J; Raymond, Lucy; Kurian, Manju A; Klein, Christine; Fung, Victor S C.
Afiliação
  • Chang FC; Movement Disorders Unit, Department of Neurology, Westmead Hospital, Sydney, Australia.
  • Westenberger A; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Dale RC; TY Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Westmead, Australia.
  • Smith M; University of Sydney, Sydney, Australia.
  • Pall HS; Department of Neurology, Birmingham Children's Hospital, Birmingham, United Kingdom.
  • Perez-Dueñas B; College of Medical and Dental Studies, University of Birmingham, Birmingham, United Kingdom.
  • Grattan-Smith P; Molecular Neurosciences, Developmental Neurosciences Program, Institute of Child Health, University College London, London, United Kingdom.
  • Ouvrier RA; Department of Child Neurology, Sant Joan de Déu Hospital, University of Barcelona, Spain.
  • Mahant N; TY Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Westmead, Australia.
  • Hanna BC; TY Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Westmead, Australia.
  • Hunter M; Sydney Medical School, University of Sydney, Australia.
  • Lawson JA; Hunter Genetics, John Hunter Hospital, Newcastle, Australia.
  • Max C; Hunter Genetics, John Hunter Hospital, Newcastle, Australia.
  • Sachdev R; Genetics of Learning Disability Service, Newcastle, Australia.
  • Meyer E; Sydney Children's Hospitals Network, Randwick, Australia.
  • Crimmins D; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Pryor D; Department of Medical Genetics, Sydney Children's Hospital, Randwick, Australia.
  • Morris JG; Molecular Neurosciences, Developmental Neurosciences Program, Institute of Child Health, University College London, London, United Kingdom.
  • Münchau A; Neurology Department, Gosford Hospital, Gosford, Australia.
  • Grozeva D; Neurology Department, St George Hospital, Kogarah, Australia.
  • Carss KJ; Movement Disorders Unit, Department of Neurology, Westmead Hospital, Sydney, Australia.
  • Raymond L; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
  • Kurian MA; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, United Kingdom.
  • Klein C; Department of Haematology, University of Cambridge, NHS Blood and Transplant Center, Cambridge, United Kingdom.
  • Fung VS; Wellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom.
Mov Disord ; 31(7): 1033-40, 2016 07.
Article em En | MEDLINE | ID: mdl-27061943
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenilil Ciclases / Transtornos dos Movimentos Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Austrália País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenilil Ciclases / Transtornos dos Movimentos Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Austrália País de publicação: Estados Unidos