Journal article
Variability in the clinical management of fatty acid oxidation disorders: results of a survey of Canadian metabolic physicians
Abstract
INTRODUCTION: There is little robust empirical evidence on which to base treatment recommendations for fatty acid oxidation disorders. While consensus guidelines are important, understanding areas where there is a lack of consensus is also critical to inform priorities for future evaluative research.
METHODS: We surveyed Canadian metabolic physicians on the treatment of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency, very long-chain …
Authors
Potter BK; Little J; Chakraborty P; Kronick JB; Evans J; Frei J; Sutherland SC; Wilson K; Wilson BJ
Journal
Journal of Inherited Metabolic Disease, Vol. 35, No. 1, pp. 115–123
Publisher
Wiley
Publication Date
January 2012
DOI
10.1007/s10545-011-9352-2
ISSN
0141-8955
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
3-Hydroxyacyl CoA DehydrogenasesAcyl-CoA DehydrogenaseAcyl-CoA Dehydrogenase, Long-ChainCanadaCarnitineCongenital Bone Marrow Failure SyndromesDietary FatsFatty AcidsHealth Knowledge, Attitudes, PracticeHumansLipid Metabolism, Inborn ErrorsLong-Chain-3-Hydroxyacyl-CoA DehydrogenaseMitochondrial DiseasesMitochondrial Trifunctional ProteinMultienzyme ComplexesMuscular DiseasesOxygenSurveys and Questionnaires