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2. Late-onset multiple acyl-CoA dehydrogenase deficiency mimicking myositis in an elderly patient: a case report. Zheng Y; Zhao Y; Zhang W; Wang Z; Yuan Y BMC Neurol; 2020 Dec; 20(1):436. PubMed ID: 33267805 [TBL] [Abstract][Full Text] [Related]
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9. Central nervous system and muscle involvement in an adolescent patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. Ishii K; Komaki H; Ohkuma A; Nishino I; Nonaka I; Sasaki M Brain Dev; 2010 Sep; 32(8):669-72. PubMed ID: 19783111 [TBL] [Abstract][Full Text] [Related]
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12. Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations. Wen B; Dai T; Li W; Zhao Y; Liu S; Zhang C; Li H; Wu J; Li D; Yan C J Neurol Neurosurg Psychiatry; 2010 Feb; 81(2):231-6. PubMed ID: 19758981 [TBL] [Abstract][Full Text] [Related]
13. Riboflavin-Responsive Multiple Acyl-CoA Dehydrogenase Deficiency Associated with Hepatoencephalomyopathy and White Matter Signal Abnormalities on Brain MRI. Vieira P; Myllynen P; Perhomaa M; Tuominen H; Keski-Filppula R; Rytky S; Risteli L; Uusimaa J Neuropediatrics; 2017 Jun; 48(3):194-198. PubMed ID: 28388738 [TBL] [Abstract][Full Text] [Related]
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