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15. Riboflavin responsive multiple acyl-CoA dehydrogenase deficiency: functional evaluation of recovery after high dose vitamin supplementation. Peluchetti D; Antozzi C; Roi S; DiDonato S; Cornelio F J Neurol Sci; 1991 Sep; 105(1):93-8. PubMed ID: 1795175 [TBL] [Abstract][Full Text] [Related]
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17. Subacute myopathy in a mature patient due to multiple acyl-coenzyme A dehydrogenase deficiency. Kaminsky P; Acquaviva-Bourdain C; Jonas J; Pruna L; Chaloub GE; Rigal O; Grignon Y; Vianey-Saban C Muscle Nerve; 2011 Mar; 43(3):444-6. PubMed ID: 21321959 [TBL] [Abstract][Full Text] [Related]
18. Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. Missaglia S; Tavian D; Moro L; Angelini C Lipids Health Dis; 2018 Nov; 17(1):254. PubMed ID: 30424791 [TBL] [Abstract][Full Text] [Related]
19. Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult. Bell RB; Brownell AK; Roe CR; Engel AG; Goodman SI; Frerman FE; Seccombe DW; Snyder FF Neurology; 1990 Nov; 40(11):1779-82. PubMed ID: 2234436 [TBL] [Abstract][Full Text] [Related]
20. Methylene-blue for riboflavin-unresponsive glutaricaciduria type II. Harpey JP; Charpentier C; Coudé M Lancet; 1986 Feb; 1(8477):391. PubMed ID: 2868334 [No Abstract] [Full Text] [Related] [Next] [New Search]