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PUBMED FOR HANDHELDS

Journal Abstract Search

301 related items for PubMed ID: 7915305

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  • 26. Diagnostic value of serum gamma-glutamyl transpeptidase activity in liver diseases in children.
    Maggiore G, Bernard O, Hadchouel M, Lemonnier A, Alagille D.
    J Pediatr Gastroenterol Nutr; 1991 Jan; 12(1):21-6. PubMed ID: 1676410
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  • 28. Ursodeoxycholic acid therapy in children with cholestatic liver disease.
    Dinler G, Koçak N, Yüce A, Gürakan F, Ozen H.
    Turk J Pediatr; 1999 Jan; 41(1):91-8. PubMed ID: 10770681
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  • 31. Lack of 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase/isomerase in fibroblasts from a child with urinary excretion of 3 beta-hydroxy-delta 5-bile acids. A new inborn error of metabolism.
    Buchmann MS, Kvittingen EA, Nazer H, Gunasekaran T, Clayton PT, Sjövall J, Björkhem I.
    J Clin Invest; 1990 Dec; 86(6):2034-7. PubMed ID: 1979336
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  • 36. Ursodeoxycholic acid treatment in children with Byler disease.
    Dinler G, Koçak N, Ozen H, Yüce A, Gürakan F.
    Pediatr Int; 1999 Dec; 41(6):662-5. PubMed ID: 10618887
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  • 37. Vanishing bile duct syndrome related to DILI and Hodgkin lymphoma overlap: A rare and severe case.
    Greca RD, Cunha-Silva M, Costa LBE, Costa JGF, Mazo DFC, Sevá-Pereira T, Nascimento MMC, Pereira IE, Oliveira FC, Faria GAS, Neto FLP, Almeida JRS.
    Ann Hepatol; 2020 Dec; 19(1):107-112. PubMed ID: 31537508
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  • 38. Neonatal cholestasis with increased 3β-monohydroxy-Δ⁵ bile acids in serum and urine: not necessarily primary oxysterol 7α hydroxylase deficiency.
    Kimura A, Nittono H, Mizuochi T, Ueki I, Kurosawa T, Muto A, Takei H.
    Clin Chim Acta; 2012 Oct 09; 413(19-20):1700-4. PubMed ID: 22652365
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  • 40. An inborn error of bile acid synthesis (3beta-hydroxy-delta5-C27-steroid dehydrogenase deficiency) presenting as malabsorption leading to rickets.
    Akobeng AK, Clayton PT, Miller V, Super M, Thomas AG.
    Arch Dis Child; 1999 May 09; 80(5):463-5. PubMed ID: 10208955
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