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 *

150 related articles for article (PubMed ID: 36579410)

  • 21. 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; 16(1):185. PubMed ID: 28950901
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A compound heterozygote case of glutaric aciduria type II in a patient carrying a novel candidate variant in ETFDH gene: A case report and literature review on compound heterozygote cases.
    Seyedtaghia MR; Jafarzadeh-Esfehani R; Hosseini S; Kobravi S; Hakkaki M; Nilipour Y
    Mol Genet Genomic Med; 2024 Jul; 12(7):e2489. PubMed ID: 38967380
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency.
    Olsen RK; Andresen BS; Christensen E; Bross P; Skovby F; Gregersen N
    Hum Mutat; 2003 Jul; 22(1):12-23. PubMed ID: 12815589
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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; 128(3):291-294. PubMed ID: 28914566
    [TBL] [Abstract][Full Text] [Related]  

  • 26. High resolution melting analysis facilitates mutation screening of ETFDH gene: applications in riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Er TK; Liang WC; Chang JG; Jong YJ
    Clin Chim Acta; 2010 May; 411(9-10):690-9. PubMed ID: 20138856
    [TBL] [Abstract][Full Text] [Related]  

  • 27. FLAD1-associated multiple acyl-CoA dehydrogenase deficiency identified by newborn screening.
    Muru K; Reinson K; Künnapas K; Lilleväli H; Nochi Z; Mosegaard S; Pajusalu S; Olsen RKJ; Õunap K
    Mol Genet Genomic Med; 2019 Sep; 7(9):e915. PubMed ID: 31392824
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, China.
    Lin Y; Zhang W; Chen Z; Lin C; Lin W; Fu Q; Peng W; Chen D
    J Pediatr Endocrinol Metab; 2021 May; 34(5):649-652. PubMed ID: 33823107
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Hypoketotic hypoglycemia without neuromuscular complications in patients with SLC25A32 deficiency.
    Al Shamsi B; Al Murshedi F; Al Habsi A; Al-Thihli K
    Eur J Hum Genet; 2022 Aug; 30(8):976-979. PubMed ID: 34764427
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Coenzyme Q10 serves to couple mitochondrial oxidative phosphorylation and fatty acid β-oxidation, and attenuates NLRP3 inflammasome activation.
    Chokchaiwong S; Kuo YT; Lin SH; Hsu YC; Hsu SP; Liu YT; Chou AJ; Kao SH
    Free Radic Res; 2018 Dec; 52(11-12):1445-1455. PubMed ID: 30003820
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Multi-organ abnormalities and mTORC1 activation in zebrafish model of multiple acyl-CoA dehydrogenase deficiency.
    Kim SH; Scott SA; Bennett MJ; Carson RP; Fessel J; Brown HA; Ess KC
    PLoS Genet; 2013 Jun; 9(6):e1003563. PubMed ID: 23785301
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Multiple acyl-CoA-dehydrogenase deficiency (MADD)--a novel mutation of electron-transferring-flavoprotein dehydrogenase ETFDH.
    Lämmer AB; Rolinski B; Ahting U; Heuss D
    J Neurol Sci; 2011 Aug; 307(1-2):166-7. PubMed ID: 21616504
    [TBL] [Abstract][Full Text] [Related]  

  • 35. An unusual presentation of type III late onset multiple-acyl-CoA dehydrogenase deficiency leading to a review of its classification system.
    Eskell M; Khan H
    J R Coll Physicians Edinb; 2022 Sep; 52(3):256-258. PubMed ID: 36369806
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Multiple acyl-COA dehydrogenase deficiency in elderly carriers.
    Macchione F; Salviati L; Bordugo A; Vincenzi M; Camilot M; Teofoli F; Pancheri E; Zordan R; Bertolin C; Rossi S; Vattemi G; Tonin P
    J Neurol; 2020 May; 267(5):1414-1419. PubMed ID: 31997039
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Severe sensory neuropathy in patients with adult-onset multiple acyl-CoA dehydrogenase deficiency.
    Wang Z; Hong D; Zhang W; Li W; Shi X; Zhao D; Yang X; Lv H; Yuan Y
    Neuromuscul Disord; 2016 Feb; 26(2):170-5. PubMed ID: 26821934
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease.
    Béhin A; Acquaviva-Bourdain C; Souvannanorath S; Streichenberger N; Attarian S; Bassez G; Brivet M; Fouilhoux A; Labarre-Villa A; Laquerrière A; Pérard L; Kaminsky P; Pouget J; Rigal O; Vanhulle C; Eymard B; Vianey-Saban C; Laforêt P
    Rev Neurol (Paris); 2016 Mar; 172(3):231-41. PubMed ID: 27038534
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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; 97(48):e13153. PubMed ID: 30508893
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.