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2. [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]
3. Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry. Clayton PT; Doig M; Ghafari S; Meaney C; Taylor C; Leonard JV; Morris M; Johnson AW Arch Dis Child; 1998 Aug; 79(2):109-15. PubMed ID: 9797589 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Diagnostic and therapeutic implications of medium-chain acylcarnitines in the medium-chain acyl-coA dehydrogenase deficiency. Roe CR; Millington DS; Maltby DA; Bohan TP; Kahler SG; Chalmers RA Pediatr Res; 1985 May; 19(5):459-66. PubMed ID: 4000772 [TBL] [Abstract][Full Text] [Related]
6. Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndrome. Bougnères PF; Rocchiccioli F; Kølvraa S; Hadchouel M; Lalau-Keraly J; Chaussain JL; Wadman SK; Gregersen N J Pediatr; 1985 Jun; 106(6):918-21. PubMed ID: 3998948 [TBL] [Abstract][Full Text] [Related]
8. Medium-chain acyl CoA dehydrogenase deficiency: electron microscopic differentiation from Reye syndrome. Santer R; Schmidt-Sommerfeld E; Leung YK; Fischer JE; Lebenthal E Eur J Pediatr; 1990 Dec; 150(2):111-4. PubMed ID: 2279505 [TBL] [Abstract][Full Text] [Related]
9. Medium-chain acyl-CoA dehydrogenase deficiency. Egidio RJ; Francis GL; Coates PM; Hale DE; Roesel A Am Fam Physician; 1989 May; 39(5):221-6. PubMed ID: 2718899 [TBL] [Abstract][Full Text] [Related]
10. Screening of the most common medium-chain acyl CoA dehydrogenase (MCAD) deficiency mutation (K329E) in the Czech newborn population. Kozàk L; Hrabincovà E; Rudolfoà J; Vràbelovà S; Freiberger T Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():49-50. PubMed ID: 11400780 [TBL] [Abstract][Full Text] [Related]
20. Frequency of 985A-to-G mutation in medium-chain acyl-CoA dehydrogenase gene among patients with sudden infant death syndrome, Reye syndrome, severe motor and intellectual disabilities and healthy newborns in Japan. Nagao M Acta Paediatr Jpn; 1996 Aug; 38(4):304-7. PubMed ID: 8840534 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]