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Journal Abstract Search

345 related items for PubMed ID: 29615056

  • 21. Multiple acyl-CoA dehydrogenation deficiency as decreased acyl-carnitine profile in serum.
    Wen B, Li D, Li W, Zhao Y, Yan C.
    Neurol Sci; 2015 Jun; 36(6):853-9. PubMed ID: 25827849
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  • 22. Neonatal-onset multiple acyl-CoA dehydrogenase deficiency (MADD) in the ETFDH gene: A case report and a literature review.
    Ding M, Liu R, Qiubo L, Zhang Y, Kong Q.
    Medicine (Baltimore); 2020 Sep 11; 99(37):e21944. PubMed ID: 32925727
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  • 23. Acute-onset multiple acyl-CoA dehydrogenase deficiency mimicking Guillain-Barré syndrome: two cases report.
    Hong D, Yu Y, Wang Y, Xu Y, Zhang J.
    BMC Neurol; 2018 Dec 26; 18(1):219. PubMed ID: 30587156
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  • 28. Neurite growth could be impaired by ETFDH mutation but restored by mitochondrial cofactors.
    Liang WC, Lin YF, Liu TY, Chang SC, Chen BH, Nishino I, Jong YJ.
    Muscle Nerve; 2017 Sep 26; 56(3):479-485. PubMed ID: 27935074
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  • 32. Clinical Features of Multiple Acyl-CoA Dehydrogenase Deficiency With ETFDH Variants in the First Korean Cases.
    Kim YJ, Ko JM, Song J, Lee KA.
    Ann Lab Med; 2018 Nov 26; 38(6):616-618. PubMed ID: 30027710
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  • 33. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.
    Olsen RK, Olpin SE, Andresen BS, Miedzybrodzka ZH, Pourfarzam M, Merinero B, Frerman FE, Beresford MW, Dean JC, Cornelius N, Andersen O, Oldfors A, Holme E, Gregersen N, Turnbull DM, Morris AA.
    Brain; 2007 Aug 26; 130(Pt 8):2045-54. PubMed ID: 17584774
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  • 34. A case of late-onset riboflavin responsive multiple acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH gene.
    Zhao ZN, Bao MX, Ma GT, Liu XM, Xu WJ, Sun ZW, Chen H, Zhu MJ.
    CNS Neurosci Ther; 2012 Nov 26; 18(11):952-4. PubMed ID: 23106979
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  • 35. Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency.
    Zhang J, Han J, Wang Y, Wu Y, Ma L, Song X, Ji G.
    Balkan Med J; 2022 Jul 22; 39(4):290-296. PubMed ID: 35734957
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  • 37. 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 22; 32(8):669-72. PubMed ID: 19783111
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  • 40. Characterization of ETFDH and PHGDH Mutations in a Patient with Mild Glutaric Aciduria Type II and Serine Deficiency.
    Ali A, Dhahouri NA, Almesmari FSA, Fathalla WM, Jasmi FA.
    Genes (Basel); 2021 May 08; 12(5):. PubMed ID: 34066864
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