A Historical Cohort Study on the Efficacy of Glucocorticoids and Riboflavin Among Patients with Late-onset Multiple Acyl-CoA Dehydrogenase Deficiency
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference18 articles.
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2. The electron transfer flavoprotein: Ubiquinone oxidoreductases;Watmough;Biochim Biophys Acta,2010
3. Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations;Wen;J Neurol Neurosurg Psychiatry,2010
4. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency;Olsen;Brain,2007
5. Folding of Desulfovibrio desulfuricans flavodoxin is accelerated by cofactor fly-casting;Muralidhara;Arch Biochem Biophys,2006
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1. Multiple Acyl-CoA Dehydrogenase Deficiency: Phenotypic and Genetic Features of a Malaysian Cohort;Journal of Clinical Neurology;2024
2. A rare condition that mimic myopathy: Late-onset glutaric acidaemia type II;Rheumatology and Immunology Research;2023-09-01
3. Case report: A novel c.1842_1845dup mutation of ETFDH in two Chinese siblings with multiple acyl-CoA dehydrogenase deficiency;Frontiers in Pediatrics;2023-01-04
4. Lipid storage myopathy due to late-onset multiple Acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH: A case report;Frontiers in Neurology;2022-12-15
5. Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic Aspects;Frontiers in Neurology;2022-03-03
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