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.
3. Acute pancreatitis in a patient with glutaric acidemia type II. Coşkun T; Göğüş S; Akçören Z; Tokatli A; Ozalp I Turk J Pediatr; 1997; 39(3):379-85. PubMed ID: 9339118 [TBL] [Abstract][Full Text] [Related]
4. Clinical and biochemical aspects of glutaric acidemia type II. Goodman SI; Loehr JP; Frerman FE Prog Clin Biol Res; 1990; 321():465-76. PubMed ID: 2326307 [No Abstract] [Full Text] [Related]
5. [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]
6. 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]
7. Recurrent hypoglycemia associated with glutaric aciduria type II in an adult. Dusheiko G; Kew MC; Joffe BI; Lewin JR; Mantagos S; Tanaka K N Engl J Med; 1979 Dec; 301(26):1405-9. PubMed ID: 514320 [TBL] [Abstract][Full Text] [Related]
8. [Carnitine deficiency in inborn errors of metabolism]. Sela BA; Lerman-Sagie T; Berkovitz M Harefuah; 1997 Nov; 133(10):419-23, 504. PubMed ID: 9418309 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Glutaric acidemia type II: heterogeneity of clinical and biochemical phenotypes. Loehr JP; Goodman SI; Frerman FE Pediatr Res; 1990 Mar; 27(3):311-5. PubMed ID: 2320399 [TBL] [Abstract][Full Text] [Related]
12. [A case report of glutaric acidemia]. Wang J; Zhang W Zhongguo Dang Dai Er Ke Za Zhi; 2006 Jun; 8(3):251. PubMed ID: 16787605 [No Abstract] [Full Text] [Related]
13. Glutaric acidemia type II: gene structure and mutations of the electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) gene. Goodman SI; Binard RJ; Woontner MR; Frerman FE Mol Genet Metab; 2002; 77(1-2):86-90. PubMed ID: 12359134 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Acute pancreatitis in a patient with glutaric acidemia type I. Lemire EG; Moroz S; Pollack B; Postuma R; Greenberg CR J Pediatr; 1996 Apr; 128(4):589-90. PubMed ID: 8618204 [No 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. 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]
19. Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutations. Goodman SI; Stein DE; Schlesinger S; Christensen E; Schwartz M; Greenberg CR; Elpeleg ON Hum Mutat; 1998; 12(3):141-4. PubMed ID: 9711871 [TBL] [Abstract][Full Text] [Related]