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 *

202 related articles for article (PubMed ID: 8617498)

  • 1. Assignment of Etfdh, Etfb, and Etfa to chromosomes 3, 7, and 13: the mouse homologs of genes responsible for glutaric acidemia type II in human.
    White RA; Dowler LL; Angeloni SV; Koeller DM
    Genomics; 1996 Apr; 33(1):131-4. PubMed ID: 8617498
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Human cDNA encoding ETF dehydrogenase (ETF:ubiquinone oxido-reductase), and mutations in glutaric acidemia type II.
    Goodman SI; Bemelen KF; Frerman FE
    Prog Clin Biol Res; 1992; 375():567-72. PubMed ID: 1438400
    [No Abstract]   [Full Text] [Related]  

  • 4. [Glutaric acidemia type II].
    Tanaka K; Ikeda Y; Finocchiaro G; Ito M
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):568-74. PubMed ID: 3270865
    [No Abstract]   [Full Text] [Related]  

  • 5. Clinical and biochemical aspects of glutaric acidemia type II.
    Goodman SI; Loehr JP; Frerman FE
    Prog Clin Biol Res; 1990; 321():465-76. PubMed ID: 2326307
    [No Abstract]   [Full Text] [Related]  

  • 6. Glutaric acidemia type II: gene structure and mutations of the electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) gene.
    Goodman SI; Binard RJ; Woontner MR; Frerman FE
    Mol Genet Metab; 2002; 77(1-2):86-90. PubMed ID: 12359134
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Glutaric aciduria type II: evidence for a defect related to the electron transfer flavoprotein or its dehydrogenase.
    Christensen E; Kølvraa S; Gregersen N
    Pediatr Res; 1984 Jul; 18(7):663-7. PubMed ID: 6433313
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new variant of glutaric aciduria type II: deficiency of beta-subunit of electron transfer flavoprotein.
    Yamaguchi S; Orii T; Maeda K; Oshima M; Hashimoto T
    J Inherit Metab Dis; 1990; 13(5):783-6. PubMed ID: 2246866
    [No Abstract]   [Full Text] [Related]  

  • 10. Newly identified forms of electron transfer flavoprotein deficiency in two patients with glutaric aciduria type II.
    Yamaguchi S; Orii T; Suzuki Y; Maeda K; Oshima M; Hashimoto T
    Pediatr Res; 1991 Jan; 29(1):60-3. PubMed ID: 2000260
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Glutaric acidemia type II: heterogeneity of clinical and biochemical phenotypes.
    Loehr JP; Goodman SI; Frerman FE
    Pediatr Res; 1990 Mar; 27(3):311-5. PubMed ID: 2320399
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Electron transfer flavoprotein deficiency: functional and molecular aspects.
    Schiff M; Froissart R; Olsen RK; Acquaviva C; Vianey-Saban C
    Mol Genet Metab; 2006 Jun; 88(2):153-8. PubMed ID: 16510302
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Glutaric aciduria type 2].
    Takusa Y; Yamaguchi S
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():743-6. PubMed ID: 12013989
    [No Abstract]   [Full Text] [Related]  

  • 14. So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager.
    Beresford MW; Pourfarzam M; Turnbull DM; Davidson JE
    Neuromuscul Disord; 2006 Apr; 16(4):269-73. PubMed ID: 16527485
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Glutaric aciduria type 2].
    Yamaguchi S
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):362-5. PubMed ID: 9590070
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. [Glutaric aciduria type 2].
    Yamaguchi S; Enkhsaikhan P
    Ryoikibetsu Shokogun Shirizu; 2001; (36):86-9. PubMed ID: 11596460
    [No Abstract]   [Full Text] [Related]  

  • 18. Glutaric acidaemia type II (multiple acyl-CoA dehydrogenation deficiency).
    Goodman SI; Frerman FE
    J Inherit Metab Dis; 1984; 7 Suppl 1():33-7. PubMed ID: 6434842
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of a mutation that abolishes quinone reduction by electron transfer flavoprotein-ubiquinone oxidoreductase.
    Beard SE; Goodman SI; Bemelen K; Frerman FE
    Hum Mol Genet; 1995 Feb; 4(2):157-61. PubMed ID: 7757062
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A case of glutaric acidemia type II (severe multiple acyl-CoA dehydrogenation disorder) with subsequent prenatal exclusion in a sibling.
    Medlock MD; Rhead WJ; Pollack L; Meredith JT; Pearl G; Reece C
    J Perinatol; 1991 Sep; 11(3):227-30. PubMed ID: 1919819
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.