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Patient care standards for primary mitochondrial disease in Australia: an Australian adaptation of the Mitochondrial Medicine Society recommendations.
Sue, Carolyn M; Balasubramaniam, Shanti; Bratkovic, Drago; Bonifant, Catherine; Christodoulou, John; Coman, David; Crawley, Karen; Edema-Hildebrand, Fabienne; Ellaway, Carolyn; Ghaoui, Roula; Kava, Maina; Kearns, Lisa S; Lee, Joy; Liang, Christina; Mackey, David A; Murray, Sean; Needham, Merrilee; Rius, Rocio; Russell, Jacqui; Smith, Nicholas J C; Thyagarajan, Dominic; Wools, Christine.
Afiliação
  • Sue CM; Department of Neurology, Royal North Shore Hospital, Northern Sydney Local Health District, Sydney, New South Wales, Australia.
  • Balasubramaniam S; Department of Neurogenetics, Kolling Institute, University of Sydney, Sydney, New South Wales, Australia.
  • Bratkovic D; Genetic Metabolic Disorders Service, The Children's Hospital at Westmead, Sydney Children's Hospital Network, Sydney, New South Wales, Australia.
  • Bonifant C; Discipline of Genetic Medicine, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Christodoulou J; Western Sydney Genetics Program, Children's Hospital at Westmead, Sydney, New South Wales, Australia.
  • Coman D; Metabolic Clinic, Women's and Children's Hospital, Adelaide, South Australia, Australia.
  • Crawley K; Department of Dietetics and Food Services, Queensland Children's Hospital, Brisbane, Queensland, Australia.
  • Edema-Hildebrand F; Western Sydney Genetics Program, Children's Hospital at Westmead, Sydney, New South Wales, Australia.
  • Ellaway C; Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia.
  • Ghaoui R; Discipline of Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia.
  • Kava M; Brain and Mitochondrial Research Group, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, Victoria, Australia.
  • Kearns LS; Department of Metabolic Medicine, Queensland Children's Hospital, Brisbane, Queensland, Australia.
  • Lee J; School of Medicine, University of Queensland, Brisbane, Queensland, Australia.
  • Liang C; School of Medicine, Griffith University, Brisbane, Queensland, Australia.
  • Mackey DA; Department of Neurogenetics, Kolling Institute, University of Sydney, Sydney, New South Wales, Australia.
  • Murray S; Department of Neurology, Royal North Shore Hospital, Northern Sydney Local Health District, Sydney, New South Wales, Australia.
  • Needham M; Discipline of Genetic Medicine, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
  • Rius R; Genetic Metabolic Disorders Service, Sydney Children's Hospital Network, Sydney, New South Wales, Australia.
  • Russell J; Department of Neurology, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
  • Smith NJC; Department of Neurology, Perth Children's Hospital, Perth, Western Australia, Australia.
  • Thyagarajan D; Department of Metabolic Medicine and Rheumatology, Perth Children's Hospital, Perth, Western Australia, Australia.
  • Wools C; School of Paediatrics and Child Health, University of Western Australia, Australia.
Intern Med J ; 52(1): 110-120, 2022 Jan.
Article em En | MEDLINE | ID: mdl-34505344
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Mitocondriais / Padrão de Cuidado Tipo de estudo: Diagnostic_studies / Guideline Limite: Humans País/Região como assunto: Oceania Idioma: En Ano de publicação: 2022 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: Doenças Mitocondriais / Padrão de Cuidado Tipo de estudo: Diagnostic_studies / Guideline Limite: Humans País/Região como assunto: Oceania Idioma: En Ano de publicação: 2022 Tipo de documento: Article