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.
44. Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children. Bonnet D; Martin D; Pascale De Lonlay ; Villain E; Jouvet P; Rabier D; Brivet M; Saudubray JM Circulation; 1999 Nov; 100(22):2248-53. PubMed ID: 10577999 [TBL] [Abstract][Full Text] [Related]
45. Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndrome. Corkey BE; Hale DE; Glennon MC; Kelley RI; Coates PM; Kilpatrick L; Stanley CA J Clin Invest; 1988 Sep; 82(3):782-8. PubMed ID: 3417871 [TBL] [Abstract][Full Text] [Related]
46. [Significance of carnitine analysis in clinical tests]. Kuwajima M; Kono N; Tarui S Nihon Rinsho; 1989 Dec; 48 Suppl():393-6. PubMed ID: 2621909 [No Abstract] [Full Text] [Related]
47. Frequency of G-985 mutation in medium chain acyl-coenzyme A dehydrogenase (MCAD) deficiency in sudden infant death syndrome (SIDS). Miller M; Brooks J; Forbes N; Insel R Prog Clin Biol Res; 1992; 375():495-8. PubMed ID: 1438393 [No Abstract] [Full Text] [Related]
49. Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes. Roe CR; Millington DS; Maltby DA; Kinnebrew P J Pediatr; 1986 Jan; 108(1):13-8. PubMed ID: 3944676 [TBL] [Abstract][Full Text] [Related]
50. [Reye syndrome and Reye-like syndrome]. Kimura A Nihon Rinsho; 2011 Mar; 69(3):455-9. PubMed ID: 21400838 [TBL] [Abstract][Full Text] [Related]
51. Acylcoenzyme A dehydrogenase deficiency in heart tissue from infants who died unexpectedly with fatty change in the liver. Allison F; Bennett MJ; Variend S; Engel PC Br Med J (Clin Res Ed); 1988 Jan; 296(6614):11-2. PubMed ID: 3122912 [TBL] [Abstract][Full Text] [Related]
52. Recurrent myoglobinuria as a presenting manifestation of very long chain acyl coenzyme A dehydrogenase deficiency. Straussberg R; Harel L; Varsano I; Elpeleg ON; Shamir R; Amir J Pediatrics; 1997 Jun; 99(6):894-6. PubMed ID: 9164788 [No Abstract] [Full Text] [Related]
53. Dicarboxylic aciduria, significance and prognostic indications. Treacy E; Pitt J; Eggington M; Hawkins R Eur J Pediatr; 1994 Dec; 153(12):918. PubMed ID: 7859795 [No Abstract] [Full Text] [Related]
54. MADD or drunk? Adults have inborn errors too. Stojanovic N; Walker V; Gatling W; Coppini DV Hosp Med; 2000 Mar; 61(3):212-3. PubMed ID: 10789396 [No Abstract] [Full Text] [Related]
55. Death caused by perioperative fasting and sedation in a child with unrecognized very long chain acyl-coenzyme A dehydrogenase deficiency. Roe CR; Wiltse HE; Sweetman L; Alvarado LL J Pediatr; 2000 Mar; 136(3):397-9. PubMed ID: 10700700 [TBL] [Abstract][Full Text] [Related]
56. Dissecting the spectrum of fatty acid oxidation disorders. Stanley CA J Pediatr; 1998 Mar; 132(3 Pt 1):384-6. PubMed ID: 9544886 [No Abstract] [Full Text] [Related]
59. [Metabolic crisis in an infant--is the problem in the mitochondria?]. Tyni T; Pihko H Duodecim; 2002; 118(13):1331-9. PubMed ID: 12239878 [No Abstract] [Full Text] [Related]
60. Neonatal onset of medium-chain acyl-coenzyme A dehydrogenase deficiency with confusing biochemical features. Christodoulou J; Hoare J; Hammond J; Ip WC; Wilcken B J Pediatr; 1995 Jan; 126(1):65-8. PubMed ID: 7815228 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]