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Journal Abstract Search

247 related items for PubMed ID: 420518

  • 1. Intestinal bile salts in cystic fibrosis: studies in the patient and experimental animal.
    Harries JT, Muller DP, McCollum JP, Lipson A, Roma E, Norman AP.
    Arch Dis Child; 1979 Jan; 54(1):19-24. PubMed ID: 420518
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  • 2. Conjugated bile acids in serum and secretions in response to cholecystokinin/secretin stimulation in children with cystic fibrosis.
    Robb TA, Davidson GP, Kirubakaran C.
    Gut; 1985 Nov; 26(11):1246-56. PubMed ID: 4065698
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  • 3. Excessive fecal taurine loss predisposes to taurine deficiency in cystic fibrosis.
    Thompson GN.
    J Pediatr Gastroenterol Nutr; 1988 Nov; 7(2):214-9. PubMed ID: 3351706
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  • 10. Ileal transposition into the upper jejunum affects lipid and bile salt absorption in rats.
    Tsuchiya T, Kalogeris TJ, Tso P.
    Am J Physiol; 1996 Oct; 271(4 Pt 1):G681-91. PubMed ID: 8897889
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  • 15. Intestinal absorption of the bile acid analogue 75Se-homocholic acid-taurine is increased in primary biliary cirrhosis, and reverts to normal during ursodeoxycholic acid administration.
    Lanzini A, De Tavonatti MG, Panarotto B, Scalia S, Mora A, Benini F, Baisini O, Lanzarotto F.
    Gut; 2003 Sep; 52(9):1371-5. PubMed ID: 12912872
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  • 16. Bile acid malabsorption in cystic fibrosis; membrane vesicles, a tool for revealing the role of the ileal brush border membrane.
    de Rooij FW, van den Berg JW, Sinaasappel M, Bosman-Jacobs EP, Touw-Blommesteijn AC.
    Acta Paediatr Scand Suppl; 1985 Sep; 317():28-30. PubMed ID: 3864359
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  • 17. Primary bile acid malabsorption: defective in vitro ileal active bile acid transport.
    Heubi JE, Balistreri WF, Fondacaro JD, Partin JC, Schubert WK.
    Gastroenterology; 1982 Oct; 83(4):804-11. PubMed ID: 7106511
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