156 related articles for article (PubMed ID: 10896290)
21. 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]
22. Defects of fatty-acid oxidation in muscle.
Angelini C
Baillieres Clin Endocrinol Metab; 1990 Sep; 4(3):561-82. PubMed ID: 2268228
[TBL] [Abstract][Full Text] [Related]
23. Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiency.
Olsen RK; Pourfarzam M; Morris AA; Dias RC; Knudsen I; Andresen BS; Gregersen N; Olpin SE
J Inherit Metab Dis; 2004; 27(5):671-8. PubMed ID: 15669683
[TBL] [Abstract][Full Text] [Related]
24. The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts.
Amendt BA; Rhead WJ
J Clin Invest; 1986 Jul; 78(1):205-13. PubMed ID: 3722376
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Glutaric aciduria type II: autopsy study of a case with electron-transferring flavoprotein dehydrogenase deficiency.
Kamiya M; Eimoto T; Kishimoto H; Tsudzuki T; Morishita H; Wada Y; Wakabayashi T; Hashimoto T; Goodman SI; Frerman FE
Pediatr Pathol; 1990; 10(6):1007-19. PubMed ID: 2082330
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. Riboflavin-responsive defects of beta-oxidation.
Gregersen N
J Inherit Metab Dis; 1985; 8 Suppl 1():65-9. PubMed ID: 3930843
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Preliminary evidence for the existence of specific functional assemblies between enzymes of the beta-oxidation pathway and the respiratory chain.
Parker A; Engel PC
Biochem J; 2000 Feb; 345 Pt 3(Pt 3):429-35. PubMed ID: 10642498
[TBL] [Abstract][Full Text] [Related]
32. Late-onset multiple acyl-CoA dehydrogenase deficiency: a frequently missed diagnosis?
Köppel S; Gottschalk J; Hoffmann GF; Waterham HR; Blobel H; Kölker S
Neurology; 2006 Oct; 67(8):1519. PubMed ID: 17060596
[No Abstract] [Full Text] [Related]
33. Metabolic defects caused by treatment with the tetrahydropyridine analog of haloperidol (HPTP), in baboons.
Mienie LJ; Bergh JJ; Van Staden E; Steyn SJ; Pond SM; Castagnoli N; Van der Schyf CJ
Life Sci; 1997; 61(3):265-72. PubMed ID: 9217286
[TBL] [Abstract][Full Text] [Related]
34. Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathy.
Wilson GN; de Chadarévian JP; Kaplan P; Loehr JP; Frerman FE; Goodman SI
Am J Med Genet; 1989 Mar; 32(3):395-401. PubMed ID: 2658591
[TBL] [Abstract][Full Text] [Related]
35. Kinetic methods for the study of the enzyme systems of beta-oxidation.
Reinsch J; Rojas C; McFarland JT
Arch Biochem Biophys; 1983 Nov; 227(1):21-30. PubMed ID: 6639077
[TBL] [Abstract][Full Text] [Related]
36. Delayed diagnosis of fatal medium-chain acyl-CoA dehydrogenase deficiency in a child.
Shetty AK; Craver RD; Harris JA; Schmidt-Sommerfeld E
Pediatr Emerg Care; 1999 Dec; 15(6):399-401. PubMed ID: 10608324
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Glutaric aciduria type II: in vitro studies on substrate oxidation, acyl-CoA dehydrogenases, and electron-transferring flavoprotein in cultured skin fibroblasts.
Rhead W; Mantagos S; Tanaka K
Pediatr Res; 1980 Dec; 14(12):1339-42. PubMed ID: 7208150
[TBL] [Abstract][Full Text] [Related]
39. Electron-transfer flavoprotein from pig liver mitochondria.
Hall CL
Methods Enzymol; 1981; 71 Pt C():386-90. PubMed ID: 7278661
[No Abstract] [Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]