156 related articles for article (PubMed ID: 6673498)
41. The influence of intravenous medium- and long-chain triglycerides and carnitine on the excretion of dicarboxylic acids.
Böhles H; Akçetin Z; Lehnert W
JPEN J Parenter Enteral Nutr; 1987; 11(1):46-8. PubMed ID: 3102781
[TBL] [Abstract][Full Text] [Related]
42. Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency.
Albers S; Levy HL; Irons M; Strauss AW; Marsden D
J Inherit Metab Dis; 2001 Jun; 24(3):417-8. PubMed ID: 11486912
[No Abstract] [Full Text] [Related]
43. Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency.
Bennett MJ; Allison F; Lowther GW; Gray RG; Johnston DI; Fitzsimmons JS; Manning NJ; Pollitt RJ
Prenat Diagn; 1987 Feb; 7(2):135-41. PubMed ID: 3575262
[TBL] [Abstract][Full Text] [Related]
44. Urinary excretion of C4--C10-dicarboxylic acids and antiketogenic properties of adipic acid in ketogenic-stimulated rats due to diabetes, long-chain and short-chain monocarboxylic acids.
Mortensen PB
Biochim Biophys Acta; 1981 May; 664(2):335-48. PubMed ID: 7248329
[TBL] [Abstract][Full Text] [Related]
45. The biological origin of ketotic dicarboxylic aciduria. In vivo and in vitro investigations of the omega-oxidation of C6-C16-monocarboxylic acids in unstarved, starved and diabetic rats.
Mortensen PB; Gregersen N
Biochim Biophys Acta; 1981 Dec; 666(3):394-404. PubMed ID: 6798996
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency.
Bergoffen J; Kaplan P; Hale DE; Bennett MJ; Berry GT
J Inherit Metab Dis; 1993; 16(5):851-6. PubMed ID: 8295400
[TBL] [Abstract][Full Text] [Related]
48. The biological origin of ketotic dicarboxylic aciduria. II. In vivo and in vitro investigations of the beta-oxidation of C8-C16-dicarboxylic acids in unstarved, starved and diabetic rats.
Mortensen PB; Gregersen N
Biochim Biophys Acta; 1982 Mar; 710(3):477-84. PubMed ID: 7074126
[TBL] [Abstract][Full Text] [Related]
49. Distinction of dicarboxylic aciduria due to medium-chain triglyceride feeding from that due to abnormal fatty acid oxidation and fasting in children.
Tserng KY; Griffin RL; Kerr DS
Metabolism; 1996 Feb; 45(2):162-7. PubMed ID: 8596483
[TBL] [Abstract][Full Text] [Related]
50. Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.
Duran M; Hofkamp M; Rhead WJ; Saudubray JM; Wadman SK
Pediatrics; 1986 Dec; 78(6):1052-7. PubMed ID: 3786030
[TBL] [Abstract][Full Text] [Related]
51. Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weakness.
Coates PM; Hale DE; Finocchiaro G; Tanaka K; Winter SC
J Clin Invest; 1988 Jan; 81(1):171-5. PubMed ID: 3335634
[TBL] [Abstract][Full Text] [Related]
52. Gender differences in medium-chain dicarboxylic aciduria in alcoholic men and women.
Ma X; Baraona E; Goozner BG; Lieber CS
Am J Med; 1999 Jan; 106(1):70-5. PubMed ID: 10320120
[TBL] [Abstract][Full Text] [Related]
53. Formation and degradation of dicarboxylic acids in relation to alterations in fatty acid oxidation in rats.
Mortensen PB
Biochim Biophys Acta; 1992 Feb; 1124(1):71-9. PubMed ID: 1543729
[TBL] [Abstract][Full Text] [Related]
54. Octanoylglucuronide excretion in patients with a defective oxidation of medium-chain fatty acids.
Duran M; Ketting D; van Vossen R; Beckeringh TE; Dorland L; Bruinvis L; Wadman SK
Clin Chim Acta; 1985 Nov; 152(3):253-60. PubMed ID: 4064333
[TBL] [Abstract][Full Text] [Related]
55. Possible deleterious effect of L-carnitine supplementation in a patient with mild multiple acyl-CoA dehydrogenation deficiency (ethylmalonic-adipic aciduria).
Green A; Preece MA; de Sousa C; Pollitt RJ
J Inherit Metab Dis; 1991; 14(5):691-7. PubMed ID: 1779616
[TBL] [Abstract][Full Text] [Related]
56. A study of urinary metabolites in patients with dicarboxylic aciduria for differential diagnosis.
Shimizu N; Yamaguchi S; Orii T
Acta Paediatr Jpn; 1994 Apr; 36(2):139-45. PubMed ID: 8203256
[TBL] [Abstract][Full Text] [Related]
57. 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]
58. Acquired multiple Acyl-CoA dehydrogenase deficiency in 10 horses with atypical myopathy.
Westermann CM; Dorland L; Votion DM; de Sain-van der Velden MG; Wijnberg ID; Wanders RJ; Spliet WG; Testerink N; Berger R; Ruiter JP; van der Kolk JH
Neuromuscul Disord; 2008 May; 18(5):355-64. PubMed ID: 18406615
[TBL] [Abstract][Full Text] [Related]
59. Mitochondropathy presenting with non-ketotic hypoglycaemia as 3-hydroxydicarboxylic aciduria.
Mayatepek E; Wanders RJ; Becker M; Bremer HJ; Hoffmann GF
J Inherit Metab Dis; 1995; 18(2):249-52. PubMed ID: 7564260
[No Abstract] [Full Text] [Related]
60. Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes.
Coates PM; Hale DE; Stanley CA; Corkey BE; Cortner JA
Pediatr Res; 1985 Jul; 19(7):671-6. PubMed ID: 4022673
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]