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23. Fatty liver, encephalopathy, and sudden unexpected death in early childhood due to medium-chain acyl-coenzyme A dehydrogenase deficiency. Perper JA; Ahdab-Barmada M Am J Forensic Med Pathol; 1992 Dec; 13(4):329-34. PubMed ID: 1288265 [TBL] [Abstract][Full Text] [Related]
24. Inherited metabolic diseases in the sudden infant death syndrome. Smith LJ Arch Dis Child; 1992 May; 67(5):662-3. PubMed ID: 1599313 [No Abstract] [Full Text] [Related]
25. Comment on "Whole blood levels of dodecanoic acid, a routinely detectable forensic marker for a genetic disease often misdiagnosed as sudden infant death syndrome (SIDS): MCAD deficiency". Ross KF; Guileyardo JM; Bennett MJ; Barnard JJ Am J Forensic Med Pathol; 1996 Dec; 17(4):349-50. PubMed ID: 8947364 [No Abstract] [Full Text] [Related]
26. Fatty infiltration in the liver in medium chain acyl CoA dehydrogenase deficiency. Losty HC; Lee P; Alfaham M; Gray OP; Leonard JV Arch Dis Child; 1991 Jun; 66(6):727-8. PubMed ID: 2053798 [TBL] [Abstract][Full Text] [Related]
27. Familial Reye-like syndrome: a presentation of medium-chain acyl-coenzyme A dehydrogenase deficiency. Taubman B; Hale DE; Kelley RI Pediatrics; 1987 Mar; 79(3):382-5. PubMed ID: 3822638 [TBL] [Abstract][Full Text] [Related]
28. One more thought on sudden infant death syndrome. Albers S; Levy HL Pediatrics; 2001 Apr; 107(4):809. PubMed ID: 11380009 [No Abstract] [Full Text] [Related]
31. Absence of immunoreactive enzyme protein in short-chain acylcoenzyme A dehydrogenase deficiency. Farnsworth L; Shepherd IM; Johnson MA; Bindoff LA; Turnbull DM Ann Neurol; 1990 Nov; 28(5):717-20. PubMed ID: 2260861 [TBL] [Abstract][Full Text] [Related]
32. Sudden infant death and lysinuric protein intolerance. de Klerk JB; Duran M; Huijmans JG; Mancini GM Eur J Pediatr; 1996 Mar; 155(3):256-7. PubMed ID: 8929742 [No Abstract] [Full Text] [Related]
33. Post-mortem analysis for two prevalent beta-oxidation mutations in sudden infant death. Yang Z; Lantz PE; Ibdah JA Pediatr Int; 2007 Dec; 49(6):883-7. PubMed ID: 18045290 [TBL] [Abstract][Full Text] [Related]
34. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency. Stanley CA Adv Pediatr; 1987; 34():59-88. PubMed ID: 3318304 [TBL] [Abstract][Full Text] [Related]
35. Liver fatty acids and the sudden infant death syndrome. Fogerty AC; Ford GL; Willcox ME; Clancy SL Am J Clin Nutr; 1984 Feb; 39(2):201-8. PubMed ID: 6230001 [TBL] [Abstract][Full Text] [Related]
36. Post-mortem recognition of inherited metabolic disorders from specific acylcarnitines in tissue in cases of sudden infant death. Roe CR; Millington DS; Maltby DA; Wellman RB Lancet; 1987 Feb; 1(8531):512. PubMed ID: 2881073 [No Abstract] [Full Text] [Related]
37. Fatty liver in sudden infant death autopsies. Sawaguchi T; Nishida H Am J Forensic Med Pathol; 1998 Sep; 19(3):294. PubMed ID: 9760100 [No Abstract] [Full Text] [Related]
38. The sudden infant death syndrome gene: does it exist? Opdal SH; Rognum TO Pediatrics; 2004 Oct; 114(4):e506-12. PubMed ID: 15466077 [TBL] [Abstract][Full Text] [Related]
39. [Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in 2 patients with symptoms of Reye syndrome]. Brus F; Smit GP; Knoester H; Reijngoud DJ Tijdschr Kindergeneeskd; 1988 Jun; 56(3):132-7. PubMed ID: 3046055 [TBL] [Abstract][Full Text] [Related]
40. The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy. Sims HF; Brackett JC; Powell CK; Treem WR; Hale DE; Bennett MJ; Gibson B; Shapiro S; Strauss AW Proc Natl Acad Sci U S A; 1995 Jan; 92(3):841-5. PubMed ID: 7846063 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]