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Journal Abstract Search

140 related items for PubMed ID: 10518286

  • 21. Acute respiratory distress syndrome in long-chain 3-hydroxyacyl-CoA dehydrogenase and mitochondrial trifunctional protein deficiencies.
    Lundy CT, Shield JP, Kvittingen EA, Vinorum OJ, Trimble ER, Morris AA.
    J Inherit Metab Dis; 2003; 26(6):537-41. PubMed ID: 14605499
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  • 22. Maternal acute fatty liver of pregnancy and the associated risk for long-chain 3-hydroxyacyl-coenzyme a dehydrogenase (LCHAD) deficiency in infants.
    Bellig LL.
    Adv Neonatal Care; 2004 Feb; 4(1):26-32. PubMed ID: 14988877
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  • 23. [LCHAD (long-chain 3-hydroxyacyl-CoA dehydrogenase) deficiency as a cause of sudden death of a three months old infant].
    Neuman-Łaniec M, Wierzba J, Irga N, Zaborowska-Sołtys M, Balcerska A.
    Med Wieku Rozwoj; 2002 Feb; 6(3):221-6. PubMed ID: 12637776
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  • 27. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
    Jackson S, Bartlett K, Land J, Moxon ER, Pollitt RJ, Leonard JV, Turnbull DM.
    Pediatr Res; 1991 Apr; 29(4 Pt 1):406-11. PubMed ID: 1830138
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  • 31. Molecular diagnosis for a fatal case of very long-chain acyl-CoA dehydrogenase deficiency in Hong Kong Chinese with a novel mutation: a preventable death by newborn screening.
    Siu WK, Mak CM, Siu SL, Siu TS, Pang CY, Lam CW, Kwong NS, Chan AY.
    Diagn Mol Pathol; 2012 Sep; 21(3):184-7. PubMed ID: 22847164
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  • 34. Mitochondropathy presenting with non-ketotic hypoglycaemia as 3-hydroxydicarboxylic aciduria.
    Mayatepek E, Wanders RJ, Becker M, Bremer HJ, Hoffmann GF.
    J Inherit Metab Dis; 1995 Sep; 18(2):249-52. PubMed ID: 7564260
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  • 36. A comprehensive HADHA c.1528G>C frequency study reveals high prevalence of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency in Poland.
    Piekutowska-Abramczuk D, Olsen RK, Wierzba J, Popowska E, Jurkiewicz D, Ciara E, Ołtarzewski M, Gradowska W, Sykut-Cegielska J, Krajewska-Walasek M, Andresen BS, Gregersen N, Pronicka E.
    J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S373-7. PubMed ID: 20814823
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  • 37. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a case example in developmental disabilities.
    Faulkner MS.
    J Pediatr Nurs; 1999 Dec; 14(6):359-68. PubMed ID: 10638050
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  • 38. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients.
    den Boer ME, Wanders RJ, Morris AA, IJlst L, Heymans HS, Wijburg FA.
    Pediatrics; 2002 Jan; 109(1):99-104. PubMed ID: 11773547
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  • 39. HELLP syndrome.
    Buist NR, Winter SC.
    JAMA; 1999 Feb 24; 281(8):704-5. PubMed ID: 10052438
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  • 40. Lack of correlation between fatty acid oxidation disorders and haemolysis, elevated liver enzymes, low platelets (HELLP) syndrome?
    Holub M, Bodamer OA, Item C, Mühl A, Pollak A, Stöckler-Ipsiroglu S.
    Acta Paediatr; 2005 Jan 24; 94(1):48-52. PubMed ID: 15858960
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