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23. Severe clinical course with recurrent hyperpyrexia in a patient with glutaric aciduria type I. Hauser SE; Boneh A Neuropediatrics; 1999 Feb; 30(1):51-2. PubMed ID: 10222465 [No Abstract] [Full Text] [Related]
24. Megalencephaly in the neonatal period as the initial manifestation of glutaric aciduria type I. Iafolla AK; Kahler SG J Pediatr; 1989 Jun; 114(6):1004-6. PubMed ID: 2627209 [No Abstract] [Full Text] [Related]
25. Hypothesis: a role for quinolinic acid in the neuropathology of glutaric aciduria type I. Heyes MP Can J Neurol Sci; 1987 Aug; 14(3 Suppl):441-3. PubMed ID: 2960429 [TBL] [Abstract][Full Text] [Related]
26. Vigabatrin in the treatment of glutaric aciduria type I. Francois B; Jaeken J; Gillis P J Inherit Metab Dis; 1990; 13(3):352-4. PubMed ID: 2122100 [No Abstract] [Full Text] [Related]
27. Glutaric aciduria type I with high residual glutaryl-CoA dehydrogenase activity. Pineda M; Ribes A; Busquets C; Vilaseca MA; Aracil A; Christensen E Dev Med Child Neurol; 1998 Dec; 40(12):840-2. PubMed ID: 9881681 [TBL] [Abstract][Full Text] [Related]
28. Glutaric aciduria type 1 and nonaccidental head injury. Hartley LM; Khwaja OS; Verity CM Pediatrics; 2001 Jan; 107(1):174-5. PubMed ID: 11134453 [No Abstract] [Full Text] [Related]
29. Glutaryl-CoA dehydrogenase activity determined with intact electron-transport chain: application to glutaric aciduria type II. Christensen E J Inherit Metab Dis; 1984; 7 Suppl 2():103-4. PubMed ID: 6434855 [No Abstract] [Full Text] [Related]
33. [Macrocephaly and dystonic cerebral palsy in a child with type I glutaric aciduria]. Plöchl E; Christensen E; Colombo JP; Weiss-Wichert P; Wenger E Padiatr Padol; 1991; 26(2):97-101. PubMed ID: 1945471 [TBL] [Abstract][Full Text] [Related]
34. Novel mutations of the glutaryl-CoA dehydrogenase gene in two Japanese patients with glutaric aciduria type I. Ikeda H; Kimura T; Ikegami T; Kato M; Matsunaga A; Yokoyama S; Yamaguchi S; Ohura T; Hayasaka K Am J Med Genet; 1998 Dec; 80(4):327-9. PubMed ID: 9856558 [TBL] [Abstract][Full Text] [Related]
35. Glutaric aciduria type I: enzymatic and neuroradiologic investigations of two kindreds. Amir N; Elpeleg ON; Shalev RS; Christensen E J Pediatr; 1989 Jun; 114(6):983-9. PubMed ID: 2723913 [TBL] [Abstract][Full Text] [Related]
36. Glutaric aciduria type I: a serious pitfall if diagnosed too late. Pfluger T; Weil S; Muntau A; Willemsen UF; Hahn K Eur Radiol; 1997; 7(8):1264-6. PubMed ID: 9377513 [TBL] [Abstract][Full Text] [Related]
37. Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy. Turnbull DM; Bartlett K; Eyre JA; Gardner-Medwin D; Johnson MA; Fisher J; Watmough NJ Dev Med Child Neurol; 1988 Oct; 30(5):667-72. PubMed ID: 3229565 [TBL] [Abstract][Full Text] [Related]
38. [Development of brain atrophy, therapy and therapy monitoring in glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency)]. Lawrenz-Wolf B; Herberg KP; Hoffmann GF; Hunneman DH; Lehnert W; Hanefeld F Klin Padiatr; 1993; 205(1):23-9. PubMed ID: 8445849 [TBL] [Abstract][Full Text] [Related]
39. Specific glutaryl-CoA dehydrogenating activity is deficient in cultured fibroblasts from glutaric aciduria patients. Hyman DB; Tanaka K J Clin Invest; 1984 Mar; 73(3):778-84. PubMed ID: 6423663 [TBL] [Abstract][Full Text] [Related]
40. Early prenatal diagnosis in two pregnancies at risk for glutaryl-CoA dehydrogenase deficiency. Holme E; Kyllerman M; Lindstedt S J Inherit Metab Dis; 1989; 12 Suppl 2():280-2. PubMed ID: 2512426 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]