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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 11867144)

  • 1. Neonatal screening for medium--chain acyl-CoA dehydrogenase deficiency.
    Fowler DJ; Picker J; Waisbren SE; Levy HL
    Lancet; 2002 Feb; 359(9306):628. PubMed ID: 11867144
    [No Abstract]   [Full Text] [Related]  

  • 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]  

  • 3. Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency.
    Wilcken B; Carpenter K; Wiley V
    Lancet; 2002 Feb; 359(9306):627-8. PubMed ID: 11867142
    [No Abstract]   [Full Text] [Related]  

  • 4. Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency.
    Pourfarzam M; Morris A; Appleton M; Craft A; Bartlett K
    Lancet; 2001 Sep; 358(9287):1063-4. PubMed ID: 11589939
    [TBL] [Abstract][Full Text] [Related]  

  • 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]  

  • 6. Screening for medium chain acyl-CoA dehydrogenase deficiency has still not been evaluated.
    Tanner S; Sharrard M; Cleary M; Walter J; Wraith E; Lee P; Leonard J; Morris A; McIntosh N
    BMJ; 2001 Jan; 322(7278):112. PubMed ID: 11203731
    [No Abstract]   [Full Text] [Related]  

  • 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]  

  • 8. Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies.
    Carpenter K; Wiley V; Sim KG; Heath D; Wilcken B
    Arch Dis Child Fetal Neonatal Ed; 2001 Sep; 85(2):F105-9. PubMed ID: 11517203
    [TBL] [Abstract][Full Text] [Related]  

  • 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]  

  • 11. [Screening of newborns for inborn errors of metabolism by tandem mass spectrometry].
    Simonsen H
    Ugeskr Laeger; 2002 Nov; 164(48):5607-12. PubMed ID: 12523003
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Deficiency of the fatty-acid oxidising enzyme medium-chain acyl-CoA dehydrogenase (MCAD) in an adult, detected during a neonatal screening programme].
    Derks TG; Jakobs H; Gerding A; Niezen-Koning KE; Reijngoud DJ; Smit GP
    Ned Tijdschr Geneeskd; 2004 Oct; 148(44):2185-90. PubMed ID: 15559414
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical efficacy and cost-effectiveness of newborn screening for medium chain acyl-CoA dehydrogenase deficiency using tandem mass spectrometry.
    Tran K; Banerjee S; Li H; Noorani HZ; Mensinkai S; Dooley K
    Clin Biochem; 2007 Feb; 40(3-4):235-41. PubMed ID: 17222812
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency].
    Takusa Y; Yamaguchi S
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():722-5. PubMed ID: 12013983
    [No Abstract]   [Full Text] [Related]  

  • 15. The frequency of medium-chain acyl-CoA dehydrogenase G985 mutation in the Hungarian population.
    Szalai C; Czinner A; Revai K
    Eur J Pediatr; 1996 Mar; 155(3):256. PubMed ID: 8929741
    [No Abstract]   [Full Text] [Related]  

  • 16. Medium-chain acyl-CoA dehydrogenase deficiency.
    Millington DS; Roe CR
    N Engl J Med; 1989 May; 320(18):1219. PubMed ID: 2710197
    [No Abstract]   [Full Text] [Related]  

  • 17. Prevalence of the 985A>G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in Sweden.
    Johansson A; Guthenberg C; Ahlman H; Von Döbeln U; Hagenfeldt L
    Scand J Clin Lab Invest; 1999 Jul; 59(4):289-91. PubMed ID: 10463467
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neonatal presentation of medium-chain acyl-CoA dehydrogenase deficiency in two families.
    Kirk JM; Laing IA; Smith N; Uttley WS
    J Inherit Metab Dis; 1996; 19(3):370-1. PubMed ID: 8803784
    [No Abstract]   [Full Text] [Related]  

  • 19. Medium-chain acyl-CoA dehydrogenase deficiency presenting in the neonatal period: the first Italian case.
    Burlina AB; Bennett MJ; Gregersen N; Dalla Barba B; Zacchello F
    Eur J Pediatr; 1995 Nov; 154(11):940-1. PubMed ID: 8582415
    [No Abstract]   [Full Text] [Related]  

  • 20. Diagnosis of medium chain acyl-CoA dehydrogenase deficiency in the newborn.
    Walker V; Mills GA; Radford M
    Lancet; 1990 May; 335(8700):1288-9. PubMed ID: 1971365
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.