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PUBMED FOR HANDHELDS

Journal Abstract Search

185 related items for PubMed ID: 7628085

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  • 2. Electrospray tandem mass spectrometry for analysis of acylcarnitines in dried postmortem blood specimens collected at autopsy from infants with unexplained cause of death.
    Chace DH, DiPerna JC, Mitchell BL, Sgroi B, Hofman LF, Naylor EW.
    Clin Chem; 2001; 47(7):1166-82. PubMed ID: 11427446
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  • 12. Complications in early diagnosis and treatment of two infants with long-chain fatty acid beta-oxidation defects.
    Skladal D, Sass JO, Geiger H, Geiger R, Mann C, Vreken P, Wanders RJ, Trawöger R.
    J Pediatr Gastroenterol Nutr; 2000 Oct; 31(4):448-52. PubMed ID: 11045847
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  • 13. Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disorders.
    Schmidt-Sommerfeld E, Bobrowski PJ, Penn D, Rhead WJ, Wanders RJ, Bennett MJ.
    Pediatr Res; 1998 Aug; 44(2):210-4. PubMed ID: 9702916
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  • 14. Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Bennett MJ, Weinberger MJ, Sherwood WG, Burlina AB.
    J Inherit Metab Dis; 1994 Aug; 17(3):283-6. PubMed ID: 7807934
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  • 15. Bile acylcarnitine profiles in pediatric liver disease do not interfere with the diagnosis of long-chain fatty acid oxidation defects.
    Fuda F, Narayan SB, Squires RH, Bennett MJ.
    Clin Chim Acta; 2006 May; 367(1-2):185-8. PubMed ID: 16414039
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  • 17. Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal death.
    Chalmers RA, Stanley CA, English N, Wigglesworth JS.
    J Pediatr; 1997 Aug; 131(2):220-5. PubMed ID: 9290607
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