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Journal Abstract Search

139 related items for PubMed ID: 3371142

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  • 25. Serum bile acids in cystic fibrosis patients - glycodeoxycholic acid as a potential marker of liver disease.
    Drzymała-Czyż S, Dziedzic K, Szwengiel A, Krzyżanowska-Jankowska P, Nowak JK, Nowicka A, Aringazina R, Drzymała S, Kashirskaya N, Walkowiak J.
    Dig Liver Dis; 2022 Jan; 54(1):111-117. PubMed ID: 34305015
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  • 26. Endogenous ursodeoxycholic acid and cholic acid in liver disease due to cystic fibrosis.
    Smith JL, Lewindon PJ, Hoskins AC, Pereira TN, Setchell KD, O'Connell NC, Shepherd RW, Ramm GA.
    Hepatology; 2004 Jun; 39(6):1673-82. PubMed ID: 15185309
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  • 33. Intestinal bile acid malabsorption in cystic fibrosis.
    O'Brien S, Mulcahy H, Fenlon H, O'Broin A, Casey M, Burke A, FitzGerald MX, Hegarty JE.
    Gut; 1993 Aug; 34(8):1137-41. PubMed ID: 8174969
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  • 38. Short-chain fatty acid absorption in patients with cystic fibrosis.
    Vaisman N, Tabachnik E, Sklan D.
    J Pediatr Gastroenterol Nutr; 1992 Aug; 15(2):146-9. PubMed ID: 1403462
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  • 40. Bile acid metabolism in cirrhosis. IV. Characterization of the abnormality in deoxycholic acid metabolism.
    Yoshida T, McCormick WC, Swell L, Vlahcevic ZR.
    Gastroenterology; 1975 Feb; 68(2):335-41. PubMed ID: 1116679
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