141 related articles for article (PubMed ID: 8295400)
21. Dicarboxylic aciduria during ketotic phases in various types of glycogen storage disease.
Pettersen JE; Winsnes A
Acta Paediatr Scand; 1981; 70(3):309-13. PubMed ID: 6941627
[TBL] [Abstract][Full Text] [Related]
22. Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy.
Tein I; De Vivo DC; Hale DE; Clarke JT; Zinman H; Laxer R; Shore A; DiMauro S
Ann Neurol; 1991 Sep; 30(3):415-9. PubMed ID: 1835339
[TBL] [Abstract][Full Text] [Related]
23. Diagnostic and therapeutic implications of medium-chain acylcarnitines in the medium-chain acyl-coA dehydrogenase deficiency.
Roe CR; Millington DS; Maltby DA; Bohan TP; Kahler SG; Chalmers RA
Pediatr Res; 1985 May; 19(5):459-66. PubMed ID: 4000772
[TBL] [Abstract][Full Text] [Related]
24. Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency.
Bertini E; Dionisi-Vici C; Garavaglia B; Burlina AB; Sabatelli M; Rimoldi M; Bartuli A; Sabetta G; DiDonato S
Eur J Pediatr; 1992 Feb; 151(2):121-6. PubMed ID: 1537353
[TBL] [Abstract][Full Text] [Related]
25. Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase: a cause of lethal myopathy and cardiomyopathy in early childhood.
Rocchiccioli F; Wanders RJ; Aubourg P; Vianey-Liaud C; Ijlst L; Fabre M; Cartier N; Bougneres PF
Pediatr Res; 1990 Dec; 28(6):657-62. PubMed ID: 2284166
[TBL] [Abstract][Full Text] [Related]
26. beta-Oxidation enzymes in fibroblasts from patients with 3-hydroxydicarboxylic aciduria.
Venizelos N; Ijlst L; Wanders RJ; Hagenfeldt L
Pediatr Res; 1994 Jul; 36(1 Pt 1):111-4. PubMed ID: 7936829
[TBL] [Abstract][Full Text] [Related]
27. General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases.
Gregersen N; Kølvraa S; Rasmussen K; Mortensen PB; Divry P; David M; Hobolth N
Clin Chim Acta; 1983 Aug; 132(2):181-91. PubMed ID: 6616873
[TBL] [Abstract][Full Text] [Related]
28. Feeding difficulties in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
Lund AM; Leonard JV
Arch Dis Child; 2001 Dec; 85(6):487-8. PubMed ID: 11719334
[TBL] [Abstract][Full Text] [Related]
29. Dicarboxylic aciduria: deficient [1-14C]octanoate oxidation and medium-chain acyl-CoA dehydrogenase in fibroblasts.
Rhead WJ; Amendt BA; Fritchman KS; Felts SJ
Science; 1983 Jul; 221(4605):73-5. PubMed ID: 6857268
[TBL] [Abstract][Full Text] [Related]
30. Mitochondrial fatty acid beta-oxidation in the human eye and brain: implications for the retinopathy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
Tyni T; Paetau A; Strauss AW; Middleton B; Kivelä T
Pediatr Res; 2004 Nov; 56(5):744-50. PubMed ID: 15347768
[TBL] [Abstract][Full Text] [Related]
31. 3-hydroxyacyl-CoA dehydrogenase (HAD) deficiency replaces short-chain hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency as well as medium- and short-chain hydroxyacyl-CoA dehydrogenase (M/SCHAD) deficiency as the consensus name of this fatty acid oxidation disorder.
He XY; Yang SY
Mol Genet Metab; 2007 Jun; 91(2):205-6. PubMed ID: 17434778
[No Abstract] [Full Text] [Related]
32. A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts.
Manning NJ; Olpin SE; Pollitt RJ; Webley J
J Inherit Metab Dis; 1990; 13(1):58-68. PubMed ID: 2109149
[TBL] [Abstract][Full Text] [Related]
33. Long-chain hydroxydicarboxylic aciduria, carnitine depletion and acetaminophen exposure.
Nowaczyk MJ; Whelan D; Hill RE; Clarke JT; Pollitt RJ
J Inherit Metab Dis; 2000 Mar; 23(2):188-9. PubMed ID: 10801061
[No Abstract] [Full Text] [Related]
34. Rapid diagnosis of medium-chain acyl CoA dehydrogenase deficiency by measurement of cis-4-decenoic acid in plasma.
Heales SJ; Woolf DA; Robinson P; Leonard JV
J Inherit Metab Dis; 1991; 14(5):661-7. PubMed ID: 1779611
[TBL] [Abstract][Full Text] [Related]
35. Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels.
Stanley CA; Hale DE; Coates PM; Hall CL; Corkey BE; Yang W; Kelley RI; Gonzales EL; Williamson JR; Baker L
Pediatr Res; 1983 Nov; 17(11):877-84. PubMed ID: 6646897
[TBL] [Abstract][Full Text] [Related]
36. Clinical and biochemical presentations in 20 cases of hydroxydicarboxylic aciduria.
Pollitt RJ
Prog Clin Biol Res; 1990; 321():495-502. PubMed ID: 2326308
[No Abstract] [Full Text] [Related]
37. Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patients.
Tyni T; Palotie A; Viinikka L; Valanne L; Salo MK; von Döbeln U; Jackson S; Wanders R; Venizelos N; Pihko H
J Pediatr; 1997 Jan; 130(1):67-76. PubMed ID: 9003853
[TBL] [Abstract][Full Text] [Related]
38. Quantitative measurement of total and free 3-hydroxy fatty acids in serum or plasma samples: short-chain 3-hydroxy fatty acids are not esterified.
Jones PM; Burlina AB; Bennett MJ
J Inherit Metab Dis; 2000 Nov; 23(7):745-50. PubMed ID: 11117435
[TBL] [Abstract][Full Text] [Related]
39. Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids.
Duran M; Mitchell G; de Klerk JB; de Jager JP; Hofkamp M; Bruinvis L; Ketting D; Saudubray JM; Wadman SK
J Pediatr; 1985 Sep; 107(3):397-404. PubMed ID: 4032135
[TBL] [Abstract][Full Text] [Related]
40. Oxidation of fatty acids in cultured fibroblasts: a model system for the detection and study of defects in oxidation.
Saudubray JM; Coudé FX; Demaugre F; Johnson C; Gibson KM; Nyhan WL
Pediatr Res; 1982 Oct; 16(10):877-81. PubMed ID: 7145511
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
