Multiple Acyl-CoA Dehydrogenase Deficiency (MADD)
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_1773-1
Reference10 articles.
1. Chen W, Zhang Y, Ni Y, Cai S, Zheng X, Mastaglia FL, Wu J (2019) Late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD): case reports and epidemiology of ETFDH gene mutations. BMC Neurol 19:330. https://doi.org/10.1186/s12883-019-1562-5
2. Ding M, Liu R, Qiubo L, Zhang Y, Kong Q (2020) Neonatal-onset multiple acyl-CoA dehydrogenase deficiency (MADD) in the ETFDH gene: a case report and a literature review. Medicine (Baltimore) 99:e21944. https://doi.org/10.1097/MD.0000000000021944
3. Grünert SC (2014) Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme a dehydrogenase deficiency. Orphanet J Rare Dis 9:117. https://doi.org/10.1186/s13023-014-0117-5
4. Liang WC et al (2009) ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. Neuromuscul Disord 19:212–216. https://doi.org/10.1016/j.nmd.2009.01.008
5. Macchione F et al (2020) Multiple acyl-COA dehydrogenase deficiency in elderly carriers. J Neurol 267:1414–1419. https://doi.org/10.1007/s00415-020-09729-z
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