These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 36369806)

  • 21. Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Law LK; Tang NL; Hui J; Fung SL; Ruiter J; Wanders RJ; Fok TF; Lam CW
    Clin Chim Acta; 2009 Jun; 404(2):95-9. PubMed ID: 19265687
    [TBL] [Abstract][Full Text] [Related]  

  • 22. ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Liang WC; Ohkuma A; Hayashi YK; López LC; Hirano M; Nonaka I; Noguchi S; Chen LH; Jong YJ; Nishino I
    Neuromuscul Disord; 2009 Mar; 19(3):212-6. PubMed ID: 19249206
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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; 19(7):487-493. PubMed ID: 31418342
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency.
    Cornelius N; Frerman FE; Corydon TJ; Palmfeldt J; Bross P; Gregersen N; Olsen RK
    Hum Mol Genet; 2012 Aug; 21(15):3435-48. PubMed ID: 22611163
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Late-onset MADD in Yemen caused by a novel ETFDH mutation misdiagnosed as ADEM.
    Lian L; Chen D; Li J; Tan S; Que J; Feng H; Fang Y; Chen L; Zhou H
    Mult Scler Relat Disord; 2021 Feb; 48():102689. PubMed ID: 33383363
    [TBL] [Abstract][Full Text] [Related]  

  • 26. CHIP control degradation of mutant ETF:QO through ubiquitylation in late-onset multiple acyl-CoA dehydrogenase deficiency.
    Liu XY; Chen XJ; Zhao M; Wang ZQ; Chen HZ; Li HF; Wang CJ; Wu SF; Peng C; Yin Y; Fu HX; Lin MT; Yu L; Xiong ZQ; Wu ZY; Wang N
    J Inherit Metab Dis; 2021 Mar; 44(2):450-468. PubMed ID: 33438237
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Investigation of adult-onset multiple acyl-CoA dehydrogenase deficiency associated with peripheral neuropathy.
    Huang K; Duan HQ; Li QX; Luo YB; Yang H
    Neuropathology; 2020 Dec; 40(6):531-539. PubMed ID: 32608139
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Riboflavin-responsive multiple Acyl-CoA dehydrogenation deficiency in 13 cases, and a literature review in mainland Chinese patients.
    Zhu M; Zhu X; Qi X; Weijiang D; Yu Y; Wan H; Hong D
    J Hum Genet; 2014 May; 59(5):256-61. PubMed ID: 24522293
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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; 39(4):290-296. PubMed ID: 35734957
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Late-onset MADD: a rare cause of cirrhosis and acute liver failure?
    Soldath P; Lund A; Vissing J
    Acta Myol; 2020 Mar; 39(1):19-23. PubMed ID: 32607475
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report.
    Goh LL; Lee Y; Tan ES; Lim JSC; Lim CW; Dalan R
    BMC Med Genomics; 2018 Apr; 11(1):37. PubMed ID: 29615056
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Mutation analysis for a family affected with riboflavin responsive-multiple acyl-CoA dehydrogenase deficiency].
    Lu J; Ji L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):428-32. PubMed ID: 25119904
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Generation of a human induced pluripotent stem cell line (LZUSHi002-A) from a MADD patient with ETFDH mutation.
    Li Y; Li Y; Liu H; Cheng L; Ma H; Xu X; Zhang N
    Stem Cell Res; 2022 Oct; 64():102914. PubMed ID: 36162333
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Pregnancy of a patient with multiple Acyl-CoA dehydrogenation deficiency (MADD).
    Trakadis Y; Kadlubowska D; Barnes R; Mitchell J; Spector E; Frerman F; Melancon S
    Mol Genet Metab; 2012 Aug; 106(4):491-4. PubMed ID: 22664151
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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; 84(5):659-673. PubMed ID: 30232818
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency.
    Chen HZ; Jin M; Cai NQ; Lin XD; Liu XY; Xu LQ; Lin MT; Lin F; Wang N; Wang ZQ; Xu GR
    Chin Med J (Engl); 2019 Jul; 132(13):1615-1618. PubMed ID: 31058673
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Clinical features and gene mutations in a patient with multiple aeyl-CoA dehydrogenase deficiency with severe fatty liver].
    Dai D; Wen F; Zhou S; Chen S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):191-4. PubMed ID: 27060313
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The ETFDH c.158A>G variation disrupts the balanced interplay of ESE- and ESS-binding proteins thereby causing missplicing and multiple Acyl-CoA dehydrogenation deficiency.
    Olsen RK; Brøner S; Sabaratnam R; Doktor TK; Andersen HS; Bruun GH; Gahrn B; Stenbroen V; Olpin SE; Dobbie A; Gregersen N; Andresen BS
    Hum Mutat; 2014 Jan; 35(1):86-95. PubMed ID: 24123825
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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; 38(6):616-618. PubMed ID: 30027710
    [No Abstract]   [Full Text] [Related]  

  • 40. A novel electron transfer flavoprotein dehydrogenase (ETFDH) gene mutation identified in a newborn with glutaric acidemia type II: a case report of a Chinese family.
    Ou M; Zhu L; Zhang Y; Zhang Y; Zhou J; Zhang Y; Chen X; Yang L; Li T; Su X; Hu Q; Wang W
    BMC Med Genet; 2020 May; 21(1):98. PubMed ID: 32393189
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.