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Journal Abstract Search

201 related items for PubMed ID: 33000234

  • 1. Clinical characteristics and gene mutation analysis of an adult patient with ETFDH‑related multiple acyl‑CoA dehydrogenase deficiency.
    Wang C, Lv H, Xu X, Ma Y, Li Q.
    Mol Med Rep; 2020 Nov; 22(5):4396-4402. PubMed ID: 33000234
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  • 7. Compound heterozygous mutations in electron transfer flavoprotein dehydrogenase identified in a young Chinese woman with late-onset glutaric aciduria type II.
    Xue Y, Zhou Y, Zhang K, Li L, Kayoumu A, Chen L, Wang Y, Lu Z.
    Lipids Health Dis; 2017 Sep 26; 16(1):185. PubMed ID: 28950901
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  • 8. A novel ETFDH mutation in an adult patient with late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Chen M, Peng J, Wei W, Wang R, Xu H, Liu H.
    Int J Neurosci; 2018 Mar 26; 128(3):291-294. PubMed ID: 28914566
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  • 11. ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin-Responsive Multiple Acyl-Coenzyme A Dehydrogenation Deficiency.
    Xu J, Li D, Lv J, Xu X, Wen B, Lin P, Liu F, Ji K, Shan J, Li H, Li W, Zhao Y, Zhao D, Pok JY, Yan C.
    Ann Neurol; 2018 Nov 26; 84(5):659-673. PubMed ID: 30232818
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  • 12. Molecular and Clinical Investigations on Portuguese Patients with Multiple acyl-CoA Dehydrogenase Deficiency.
    Henriques BJ, Lucas TG, Martins E, Gaspar A, Bandeira A, Nogueira C, Brandão O, Rocha H, Vilarinho L, Gomes CM.
    Curr Mol Med; 2019 Nov 26; 19(7):487-493. PubMed ID: 31418342
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  • 15. 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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  • 19. Long-term outcomes of a patient with late-onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutations in ETFDH: A case report.
    Wang J, Wu JC, Yu XE, Han YZ, Yang RM.
    Medicine (Baltimore); 2018 Nov 08; 97(48):e13153. PubMed ID: 30508893
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