These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
103 related articles for article (PubMed ID: 7408214)
21. Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency. Bhala A; Willi SM; Rinaldo P; Bennett MJ; Schmidt-Sommerfeld E; Hale DE J Pediatr; 1995 Jun; 126(6):910-5. PubMed ID: 7776094 [TBL] [Abstract][Full Text] [Related]
22. A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria. Bartlett K; Ng H; Leonard JV Clin Chim Acta; 1980 Jan; 100(2):183-6. PubMed ID: 6766095 [TBL] [Abstract][Full Text] [Related]
23. The treatment of isovaleric acidemia with glycine supplement. Naglak M; Salvo R; Madsen K; Dembure P; Elsas L Pediatr Res; 1988 Jul; 24(1):9-13. PubMed ID: 3137519 [TBL] [Abstract][Full Text] [Related]
24. The glycine Kühn S; Williams ME; Dercksen M; Sass JO; van der Sluis R Comput Struct Biotechnol J; 2023; 21():1236-1248. PubMed ID: 36817957 [TBL] [Abstract][Full Text] [Related]
25. Ethylmalonic/adipic aciduria: effects of oral medium-chain triglycerides, carnitine, and glycine on urinary excretion of organic acids, acylcarnitines, and acylglycines. Rinaldo P; Welch RD; Previs SF; Schmidt-Sommerfeld E; Gargus JJ; O'Shea JJ; Zinn AB Pediatr Res; 1991 Sep; 30(3):216-21. PubMed ID: 1945558 [TBL] [Abstract][Full Text] [Related]
26. Tiglylglycine excreted in urine in disorders of isoleucine metabolism and the respiratory chain measured by stable isotope dilution GC-MS. Bennett MJ; Powell S; Swartling DJ; Gibson KM Clin Chem; 1994 Oct; 40(10):1879-83. PubMed ID: 7923765 [TBL] [Abstract][Full Text] [Related]
28. Suberylglycine excretion in the urine from a patient with dicarboxylic aciduria. Gregersen N; Lauritzen R; Rasmussen K Clin Chim Acta; 1976 Aug; 70(3):417-25. PubMed ID: 947635 [TBL] [Abstract][Full Text] [Related]
29. D-glyceric acidemia: an inborn error associated with fructose metabolism. Duran M; Beemer FA; Bruinvis L; Ketting D; Wadman SK Pediatr Res; 1987 May; 21(5):502-6. PubMed ID: 3588091 [TBL] [Abstract][Full Text] [Related]
30. 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]
31. The acyl-CoA dehydrogenation deficiencies. Recent advances in the enzymic characterization and understanding of the metabolic and pathophysiological disturbances in patients with acyl-CoA dehydrogenation deficiencies. Gregersen N Scand J Clin Lab Invest Suppl; 1985; 174():1-60. PubMed ID: 3892650 [TBL] [Abstract][Full Text] [Related]
32. d-Glyceric aciduria does not cause nonketotic hyperglycinemia: A historic co-occurrence. Swanson MA; Garcia SM; Spector E; Kronquist K; Creadon-Swindell G; Walter M; Christensen E; Van Hove JLK; Sass JO Mol Genet Metab; 2017 Jun; 121(2):80-82. PubMed ID: 28462797 [TBL] [Abstract][Full Text] [Related]
33. [2-Methyl-3-oxovaleric acid: a characteristic metabolite in propionic acidemia]. Lehnert W; Junker A Clin Chim Acta; 1980 May; 104(1):47-51. PubMed ID: 7389125 [TBL] [Abstract][Full Text] [Related]
34. Glycine therapy in isovaleric acidemia. Yudkoff M; Cohn RM; Puschak R; Rothman R; Segal S J Pediatr; 1978 May; 92(5):813-7. PubMed ID: 641635 [TBL] [Abstract][Full Text] [Related]
35. Intravenous L-carnitine and acetyl-L-carnitine in medium-chain acyl-coenzyme A dehydrogenase deficiency and isovaleric acidemia. Van Hove JL; Kahler SG; Millington DS; Roe DS; Chace DH; Heales SJ; Roe CR Pediatr Res; 1994 Jan; 35(1):96-101. PubMed ID: 8134205 [TBL] [Abstract][Full Text] [Related]
36. 2-Methylbutyryl-coenzyme A dehydrogenase deficiency: functional and molecular studies on a defect in isoleucine catabolism. Sass JO; Ensenauer R; Röschinger W; Reich H; Steuerwald U; Schirrmacher O; Engel K; Häberle J; Andresen BS; Mégarbané A; Lehnert W; Zschocke J Mol Genet Metab; 2008 Jan; 93(1):30-5. PubMed ID: 17945527 [TBL] [Abstract][Full Text] [Related]
37. Demonstration of a specific mitochondrial isovaleryl-CoA dehydrogenase deficiency in fibroblasts from patients with isovaleric acidemia. Rhead WJ; Tanaka K Proc Natl Acad Sci U S A; 1980 Jan; 77(1):580-3. PubMed ID: 6928646 [TBL] [Abstract][Full Text] [Related]
38. Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine. Rinaldo P; O'Shea JJ; Coates PM; Hale DE; Stanley CA; Tanaka K N Engl J Med; 1988 Nov; 319(20):1308-13. PubMed ID: 3054550 [TBL] [Abstract][Full Text] [Related]
39. Population screening for medium-chain acyl-CoA dehydrogenase deficiency: analysis of medium-chain fatty acids and acylglycines in blood spots. Bennett MJ; Ragni MC; Ostfeld RJ; Santer R; Schmidt-Sommerfeld E Ann Clin Biochem; 1994 Jan; 31 ( Pt 1)():72-7. PubMed ID: 8154855 [TBL] [Abstract][Full Text] [Related]