BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 2234436)

  • 1. Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult.
    Bell RB; Brownell AK; Roe CR; Engel AG; Goodman SI; Frerman FE; Seccombe DW; Snyder FF
    Neurology; 1990 Nov; 40(11):1779-82. PubMed ID: 2234436
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Systemic carnitine deficiency due to lack of electron transfer flavoprotein:ubiquinone oxidoreductase.
    Di Donato S; Frerman FE; Rimoldi M; Rinaldo P; Taroni F; Wiesmann UN
    Neurology; 1986 Jul; 36(7):957-63. PubMed ID: 3714057
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 130(Pt 8):2045-54. PubMed ID: 17584774
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts.
    Frerman FE; Goodman SI
    Proc Natl Acad Sci U S A; 1985 Jul; 82(13):4517-20. PubMed ID: 2989828
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The importance of recognizing secondary carnitine deficiency in organic acidaemias: case report in glutaric acidaemia type II.
    Mandel H; Africk D; Blitzer M; Shapira E
    J Inherit Metab Dis; 1988; 11(4):397-402. PubMed ID: 2468819
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II)].
    Tojo M; Gunji T; Yamaguchi S; Shimizu N; Koga Y; Nonaka I
    No To Hattatsu; 2000 Mar; 32(2):163-8. PubMed ID: 10723193
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Expression of human electron transfer flavoprotein-ubiquinone oxidoreductase from a baculovirus vector: kinetic and spectral characterization of the human protein.
    Simkovic M; Degala GD; Eaton SS; Frerman FE
    Biochem J; 2002 Jun; 364(Pt 3):659-67. PubMed ID: 12049629
    [TBL] [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. 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]  

  • 13. Electron-transfer flavoprotein-ubiquinone oxidoreductase from pig liver: purification and molecular, redox, and catalytic properties.
    Beckmann JD; Frerman FE
    Biochemistry; 1985 Jul; 24(15):3913-21. PubMed ID: 4052375
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reaction of electron-transfer flavoprotein ubiquinone oxidoreductase with the mitochondrial respiratory chain.
    Frerman FE
    Biochim Biophys Acta; 1987 Sep; 893(2):161-9. PubMed ID: 3620453
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

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

  • 17. The inborn errors of mitochondrial fatty acid oxidation.
    Vianey-Liaud C; Divry P; Gregersen N; Mathieu M
    J Inherit Metab Dis; 1987; 10 Suppl 1():159-200. PubMed ID: 3119938
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

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

    [Next]    [New Search]
    of 10.