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.
43. Glutaric aciduria type II: report on a previously undescribed metabolic disorder. Przyrembel H; Wendel U; Becker K; Bremer HJ; Bruinvis L; Ketting D; Wadman SK Clin Chim Acta; 1976 Jan; 66(2):227-39. PubMed ID: 1245071 [TBL] [Abstract][Full Text] [Related]
44. 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]
45. The occurrence of substituted 3-methyl-3-hydroxyglutaric acids in urine in propionic acidaemia and in beta-ketothiolase deficiency. Pollitt RJ Biomed Mass Spectrom; 1983 Apr; 10(4):253-7. PubMed ID: 6133567 [TBL] [Abstract][Full Text] [Related]
46. Calcium levulinate medication. A pitfall in the diagnosis of organic acidurias. Kolvraa S; Gregersen N; Christensen E; Gron I Clin Chim Acta; 1977 Jun; 77(2):197-201. PubMed ID: 890942 [TBL] [Abstract][Full Text] [Related]
50. CAD MIKES: a new method for a rapid and unequivocal structural identification of organic acids in biological fluids. A first application to a case of methylmalonic aciduria. Rinaldo P; Chiandetti L; Zacchello F; Daolio S; Traldi P Biomed Mass Spectrom; 1984 Dec; 11(12):643-6. PubMed ID: 6529595 [TBL] [Abstract][Full Text] [Related]
51. A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts. Burlina AB; Dionisi-Vici C; Bennett MJ; Gibson KM; Servidei S; Bertini E; Hale DE; Schmidt-Sommerfeld E; Sabetta G; Zacchello F J Pediatr; 1994 Jan; 124(1):79-86. PubMed ID: 8283379 [TBL] [Abstract][Full Text] [Related]
54. Selective screening for inborn errors of metabolism on clinical patients using tandem mass spectrometry in China: a four-year report. Han LS; Ye J; Qiu WJ; Gao XL; Wang Y; Gu XF J Inherit Metab Dis; 2007 Aug; 30(4):507-14. PubMed ID: 17347912 [TBL] [Abstract][Full Text] [Related]
56. The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts. Amendt BA; Rhead WJ J Clin Invest; 1986 Jul; 78(1):205-13. PubMed ID: 3722376 [TBL] [Abstract][Full Text] [Related]
57. A case of ethylmalonic encephalopathy with atypical clinical and biochemical presentation. Di Rocco M; Caruso U; Briem E; Rossi A; Allegri AE; Buzzi D; Tiranti V Mol Genet Metab; 2006 Dec; 89(4):395-7. PubMed ID: 16828325 [TBL] [Abstract][Full Text] [Related]
58. Organic acid and acylcarnitine profiles of glutaric aciduria type I. Matsumoto M; Matsumoto I; Shinka T; Kuhara T; Imamura H; Shimao S; Okada T Acta Paediatr Jpn; 1990 Feb; 32(1):76-82. PubMed ID: 2109491 [TBL] [Abstract][Full Text] [Related]
59. Methylmalonic/beta-hydroxy-n-valeric aciduria due to methylmalonyl-CoA mutase deficiency. Goodman SI; McCabe ER; Fennessey PV; Miles BS; Mace JW; Jellum E Clin Chim Acta; 1978 Aug; 87(3):441-9. PubMed ID: 28187 [TBL] [Abstract][Full Text] [Related]
60. Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: another possible case of glutaric aciduria type II. Gregersen N; Kølvraa S; Rasmussen K; Christensen E; Brandt NJ; Ebbesen F; Hansen FH J Inherit Metab Dis; 1980; 3(3):67-72. PubMed ID: 6158623 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]