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2. Screening for medium chain acyl-CoA dehydrogenase deficiency is being evaluated. Grosse S BMJ; 2001 Apr; 322(7293):1062. PubMed ID: 11349662 [No Abstract] [Full Text] [Related]
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5. Sweet and sour aspects of medium-chain acyl CoA dehydrogenase deficiency. Commentary on K. Yusuf et al.: Neonatal ventricular tachyarrhythmias in medium chain acyl-CoA dehydrogenase deficiency (Neonatology 2010;98:260-264). Derks TG Neonatology; 2010; 98(3):265-7. PubMed ID: 20414004 [No Abstract] [Full Text] [Related]
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7. 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]
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9. 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]
10. Population screening for medium-chain acyl-CoA dehydrogenase deficiency: analysis of medium-chain fatty acids and acylglycines in blood spots. Bennett MJ; Ragni MC; Ostfeld RJ; Santer R; Schmidt-Sommerfeld E Ann Clin Biochem; 1994 Jan; 31 ( Pt 1)():72-7. PubMed ID: 8154855 [TBL] [Abstract][Full Text] [Related]
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