Parikh, S;
Goldstein, A;
Karaa, A;
Koenig, MK;
Anselm, I;
Brunel-Guitton, C;
Christodoulou, J;
... Chinnery, PF; + view all
(2017)
Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Genetics in Medicine
, 19
, Article 1380. 10.1038/gim.2017.107.
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Abstract
The purpose of this statement is to provide consensus-based recommendations for optimal management and care for patients with primary mitochondrial disease. This statement is intended for physicians who are engaged in the diagnosis and management of these patients. Working group members were appointed by the Mitochondrial Medicine Society. The panel included members with several different areas of expertise. The panel members utilized surveys and the Delphi method to reach consensus. We anticipate that this statement will need to be updated as the field continues to evolve. Consensus-based recommendations are provided for the routine care and management of patients with primary genetic mitochondrial disease.
| Type: | Article |
|---|---|
| Title: | Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society |
| Location: | United States |
| Open access status: | An open access version is available from UCL Discovery |
| DOI: | 10.1038/gim.2017.107 |
| Publisher version: | http://doi.org/10.1038/gim.2017.107 |
| Language: | English |
| Additional information: | This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions. |
| Keywords: | care guidelines; consensus criteria; Delphi method; mitochondrial disease; treatment |
| UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Genetics and Genomic Medicine Dept |
| URI: | https://discovery.ucl.ac.uk/id/eprint/1568709 |
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