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A genetic basis is identified in 74% cases of paediatric hyperCKaemia without weakness presenting to a tertiary paediatric neuromuscular centre.
Wong, Wui-Kwan; Bryen, Samantha J; Bournazos, Adam; Yasa, Joe; Lemckert, Frances; Bommireddipall, Shobhana; Waddell, Leigh B; Menezes, Manoj P; Webster, Richard; Davis, Mark; Liang, Christina; Cooper, Sandra T; Jones, Kristi J.
Afiliação
  • Wong WK; Kids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, New South Wales, Australia; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia. Electronic address: wuikwan.wong@health.nsw.gov.au.
  • Bryen SJ; Kids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, New South Wales, Australia; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia.
  • Bournazos A; Kids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, New South Wales, Australia; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia.
  • Yasa J; Kids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, New South Wales, Australia; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia.
  • Lemckert F; Kids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, New South Wales, Australia; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia.
  • Bommireddipall S; Kids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, New South Wales, Australia; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia.
  • Waddell LB; Kids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, New South Wales, Australia; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia.
  • Menezes MP; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia; Department of Paediatric Neurology, Children's Hospital at Westmead, Sydney, New South Wales, Australia.
  • Webster R; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia; Department of Paediatric Neurology, Children's Hospital at Westmead, Sydney, New South Wales, Australia.
  • Davis M; Department of Diagnostic Genomics, PathWest Laboratory Medicine, QEII Medical Centre, Perth, Western Australia, Australia.
  • Liang C; Department of Neurology, Royal North Shore Hospital, Sydney, New South Wales, Australia.
  • Cooper ST; Kids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, New South Wales, Australia; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia; Children's Medical Research Institute, 214 Hawkesbury Road, Westmead, NSW2145, Australia.
  • Jones KJ; Kids Neuroscience Centre, The Children's Hospital at Westmead, Sydney, New South Wales, Australia; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia; Children's Medical Research Institute, 214 Hawkesbury Road, Westmead, NSW2145, Australia; Department
Neuromuscul Disord ; 32(9): 707-717, 2022 09.
Article em En | MEDLINE | ID: mdl-35948506

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Musculares / Doenças Neuromusculares Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Female / Humans / Male Idioma: En Revista: Neuromuscul Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Musculares / Doenças Neuromusculares Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Female / Humans / Male Idioma: En Revista: Neuromuscul Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article