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7. Human cDNA encoding ETF dehydrogenase (ETF:ubiquinone oxido-reductase), and mutations in glutaric acidemia type II. Goodman SI; Bemelen KF; Frerman FE Prog Clin Biol Res; 1992; 375():567-72. PubMed ID: 1438400 [No Abstract] [Full Text] [Related]
8. Glutaric acidemia type II: a form with deleterious intrauterine effects. Goodman SI; Reale M; Berlow S J Pediatr; 1983 Mar; 102(3):411-3. PubMed ID: 6681838 [No Abstract] [Full Text] [Related]
9. [Glutaric acidemia type II]. Tanaka K; Ikeda Y; Finocchiaro G; Ito M Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):568-74. PubMed ID: 3270865 [No Abstract] [Full Text] [Related]
12. Symmetric hypoplasia of the temporal cerebral lobes in an infant with glutaric aciduria type II (multiple acyl-coenzyme A dehydrogenase deficiency). Stöckler S; Radner H; Karpf EF; Hauer A; Ebner F J Pediatr; 1994 Apr; 124(4):601-4. PubMed ID: 8151478 [TBL] [Abstract][Full Text] [Related]
13. Glutaric aciduria type II: treatment with riboflavine, carnitine and insulin. Mooy PD; Przyrembel H; Giesberts MA; Scholte HR; Blom W; van Gelderen HH Eur J Pediatr; 1984 Dec; 143(2):92-5. PubMed ID: 6394338 [TBL] [Abstract][Full Text] [Related]
14. Hypoketotic hypoglycemic coma in a 21-month-old child. Hostetler MA; Arnold GL; Mooney R; Bennett MJ; Rinaldo P; Roe CR Ann Emerg Med; 1999 Sep; 34(3):394-8. PubMed ID: 10459098 [TBL] [Abstract][Full Text] [Related]
15. Glutaric aciduria Type II. Sweetman L; Nyhan WL; Tauner DA; Merritt TA; Singh M J Pediatr; 1980 Jun; 96(6):1020-6. PubMed ID: 7373461 [TBL] [Abstract][Full Text] [Related]
16. Quantification of glutaric acid by isotope dilution mass spectrometry for patients with glutaric acidemia type I: selected ion monitoring vs. selected ion storage. Hagen T; Korson MS Clin Chim Acta; 1999 Apr; 282(1-2):185-95. PubMed ID: 10340447 [TBL] [Abstract][Full Text] [Related]
17. Riboflavin responsive glutaric aciduria type II. Gregersen N; Rhead W; Christensen E Prog Clin Biol Res; 1990; 321():477-94. PubMed ID: 2183240 [No Abstract] [Full Text] [Related]
18. Determination of organic acids by capillary electrophoresis in screening of organic acidurias. Jariego CM; Hernanz A Clin Chem; 1996 Mar; 42(3):477-8. PubMed ID: 8598123 [No Abstract] [Full Text] [Related]
19. Assignment of Etfdh, Etfb, and Etfa to chromosomes 3, 7, and 13: the mouse homologs of genes responsible for glutaric acidemia type II in human. White RA; Dowler LL; Angeloni SV; Koeller DM Genomics; 1996 Apr; 33(1):131-4. PubMed ID: 8617498 [TBL] [Abstract][Full Text] [Related]
20. A case of glutaric acidemia type II (severe multiple acyl-CoA dehydrogenation disorder) with subsequent prenatal exclusion in a sibling. Medlock MD; Rhead WJ; Pollack L; Meredith JT; Pearl G; Reece C J Perinatol; 1991 Sep; 11(3):227-30. PubMed ID: 1919819 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]