443 related articles for article (PubMed ID: 3119938)
1. 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]
2. 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]
3. 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]
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. 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]
6. Antenatal expression of multiple acyl-CoA dehydrogenase deficiency.
Vianey-Saban C; Bouvier R; Cochat P; Buenerd A; Divry P; Dumoulin R; Cordier MP
J Inherit Metab Dis; 2000 Jun; 23(4):345-8. PubMed ID: 10896290
[No Abstract] [Full Text] [Related]
7. 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]
8. [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]
9. [Glutaric aciduria type 2].
Yamaguchi S
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):362-5. PubMed ID: 9590070
[No Abstract] [Full Text] [Related]
10. 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]
11. C6-C10-dicarboxylic aciduria: investigations of a patient with riboflavin responsive multiple acyl-CoA dehydrogenation defects.
Gregersen N; Wintzensen H; Christensen SK; Christensen MF; Brandt NJ; Rasmussen K
Pediatr Res; 1982 Oct; 16(10):861-8. PubMed ID: 7145508
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Neuropsychiatric manifestations of defect in mitochondrial beta oxidation response to riboflavin.
Triggs WJ; Roe CR; Rhead WJ; Hanson SK; Lin SN; Willmore LJ
J Neurol Neurosurg Psychiatry; 1992 Mar; 55(3):209-11. PubMed ID: 1564483
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disorders.
Schmidt-Sommerfeld E; Bobrowski PJ; Penn D; Rhead WJ; Wanders RJ; Bennett MJ
Pediatr Res; 1998 Aug; 44(2):210-4. PubMed ID: 9702916
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Prenatal diagnosis of glutaric acidemias.
Goodman SI
Prenat Diagn; 2001 Dec; 21(13):1167-8. PubMed ID: 11787045
[No Abstract] [Full Text] [Related]
19. [Glutaric aciduria type 2].
Yamaguchi S; Enkhsaikhan P
Ryoikibetsu Shokogun Shirizu; 2001; (36):86-9. PubMed ID: 11596460
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
