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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.
Affiliation
  • 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 in En | MEDLINE | ID: mdl-34505344
ABSTRACT
This document provides consensus-based recommendations for general physicians and primary care physicians who diagnose and manage patients with mitochondrial diseases (MD). It builds on previous international guidelines, with particular emphasis on clinical management in the Australian setting. This statement was prepared by a working group of medical practitioners, nurses and allied health professionals with clinical expertise and experience in managing Australian patients with MD. As new treatments and management plans emerge, these consensus-based recommendations will continue to evolve, but current standards of care are summarised in this document.
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Full text: 1 Database: MEDLINE Main subject: Mitochondrial Diseases / Standard of Care Type of study: Diagnostic_studies / Guideline Limits: Humans Country/Region as subject: Oceania Language: En Journal: Intern Med J Journal subject: MEDICINA INTERNA Year: 2022 Type: Article Affiliation country: Australia
Fulltext
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Full text: 1 Database: MEDLINE Main subject: Mitochondrial Diseases / Standard of Care Type of study: Diagnostic_studies / Guideline Limits: Humans Country/Region as subject: Oceania Language: En Journal: Intern Med J Journal subject: MEDICINA INTERNA Year: 2022 Type: Article Affiliation country: Australia