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Journal Abstract Search

323 related items for PubMed ID: 9500542

  • 21. Benign recurrent intrahepatic cholestasis.
    Luketic VA, Shiffman ML.
    Clin Liver Dis; 2004 Feb; 8(1):133-49, vii. PubMed ID: 15062197
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  • 22. Progressive familial intrahepatic cholestasis type 1 and extrahepatic features: no catch-up of stature growth, exacerbation of diarrhea, and appearance of liver steatosis after liver transplantation.
    Lykavieris P, van Mil S, Cresteil D, Fabre M, Hadchouel M, Klomp L, Bernard O, Jacquemin E.
    J Hepatol; 2003 Sep; 39(3):447-52. PubMed ID: 12927934
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  • 23. [Benign recurrent intrahepatic cholestasis type-II--a rare cause of direct hyperbilirubinemia exacerbations with hepatic fibrosis].
    Mizrahi M, Lalazar G, Horwich Y, Adar T, Safadi R.
    Harefuah; 2008 May; 147(5):381-3, 480. PubMed ID: 18770956
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  • 25. Cholestatic liver diseases: slow progress in understanding and treating slowly progressive disorders.
    Vleggaar FP, Van Ooteghem NA, Van Buuren HR, Van Berge Henegouwen GP.
    Scand J Gastroenterol Suppl; 2000 May; (232):86-92. PubMed ID: 11232499
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  • 30. Characterization of the P5 subfamily of P-type transport ATPases in mice.
    Schultheis PJ, Hagen TT, O'Toole KK, Tachibana A, Burke CR, McGill DL, Okunade GW, Shull GE.
    Biochem Biophys Res Commun; 2004 Oct 22; 323(3):731-8. PubMed ID: 15381061
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  • 31. Effects of bezafibrate on dyslipidemia with cholestasis in children with familial intrahepatic cholestasis-1 deficiency manifesting progressive familial intrahepatic cholestasis.
    Nagasaka H, Yorifuji T, Hirano K, Ota A, Toyama-Nakagawa Y, Takatani T, Tsukahara H, Kobayashi K, Takayanagi M, Inomata Y, Uemoto S, Miida T.
    Metabolism; 2009 Jan 22; 58(1):48-54. PubMed ID: 19059530
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  • 32. A flippase-independent function of ATP8B1, the protein affected in familial intrahepatic cholestasis type 1, is required for apical protein expression and microvillus formation in polarized epithelial cells.
    Verhulst PM, van der Velden LM, Oorschot V, van Faassen EE, Klumperman J, Houwen RH, Pomorski TG, Holthuis JC, Klomp LW.
    Hepatology; 2010 Jun 22; 51(6):2049-60. PubMed ID: 20512993
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  • 34. Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24.
    Floreani A, Molaro M, Mottes M, Sangalli A, Baragiotta A, Roda A, Naccarato R, Clementi M.
    Am J Med Genet; 2000 Dec 18; 95(5):450-3. PubMed ID: 11146465
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  • 36. [Genetic cholestasis].
    Ciocca M, Alvarez F.
    Arch Argent Pediatr; 2009 Aug 18; 107(4):340-6. PubMed ID: 19753442
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  • 38. The type 4 subfamily of P-type ATPases, putative aminophospholipid translocases with a role in human disease.
    Paulusma CC, Oude Elferink RP.
    Biochim Biophys Acta; 2005 Jun 30; 1741(1-2):11-24. PubMed ID: 15919184
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  • 39. ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy.
    Müllenbach R, Bennett A, Tetlow N, Patel N, Hamilton G, Cheng F, Chambers J, Howard R, Taylor-Robinson SD, Williamson C.
    Gut; 2005 Jun 30; 54(6):829-34. PubMed ID: 15888793
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  • 40. Differential effects of progressive familial intrahepatic cholestasis type 1 and benign recurrent intrahepatic cholestasis type 1 mutations on canalicular localization of ATP8B1.
    Folmer DE, van der Mark VA, Ho-Mok KS, Oude Elferink RP, Paulusma CC.
    Hepatology; 2009 Nov 30; 50(5):1597-605. PubMed ID: 19731236
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