These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

173 related items for PubMed ID: 9272158

  • 1. Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21-q22.
    Arnell H, Nemeth A, Annerén G, Dahl N.
    Hum Genet; 1997 Sep; 100(3-4):378-81. PubMed ID: 9272158
    [Abstract] [Full Text] [Related]

  • 2. Locus heterogeneity in progressive familial intrahepatic cholestasis.
    Strautnieks SS, Kagalwalla AF, Tanner MS, Gardiner RM, Thompson RJ.
    J Med Genet; 1996 Oct; 33(10):833-6. PubMed ID: 8933336
    [Abstract] [Full Text] [Related]

  • 3. Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64.
    Sinke RJ, Carlton VE, Juijn JA, Delhaas T, Bull L, van Berge Henegouwen GP, van Hattum J, Keller KM, Sinaasappel M, Bijleveld CM, Knol IE, Ploos van Amstel HK, Pearson PL, Berger R, Freimer NB, Houwen RH.
    Hum Genet; 1997 Sep; 100(3-4):382-7. PubMed ID: 9272159
    [Abstract] [Full Text] [Related]

  • 4. Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region.
    Carlton VE, Knisely AS, Freimer NB.
    Hum Mol Genet; 1995 Jun; 4(6):1049-53. PubMed ID: 7655458
    [Abstract] [Full Text] [Related]

  • 5. Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on chromosome 2q24.
    Strautnieks SS, Kagalwalla AF, Tanner MS, Knisely AS, Bull L, Freimer N, Kocoshis SA, Gardiner RM, Thompson RJ.
    Am J Hum Genet; 1997 Sep; 61(3):630-3. PubMed ID: 9326328
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity.
    Bull LN, Carlton VE, Stricker NL, Baharloo S, DeYoung JA, Freimer NB, Magid MS, Kahn E, Markowitz J, DiCarlo FJ, McLoughlin L, Boyle JT, Dahms BB, Faught PR, Fitzgerald JF, Piccoli DA, Witzleben CL, O'Connell NC, Setchell KD, Agostini RM, Kocoshis SA, Reyes J, Knisely AS.
    Hepatology; 1997 Jul 18; 26(1):155-64. PubMed ID: 9214465
    [Abstract] [Full Text] [Related]

  • 8. Genetic cholestasis: lessons from the molecular physiology of bile formation.
    Jansen PL, Müller M.
    Can J Gastroenterol; 2000 Mar 18; 14(3):233-8. PubMed ID: 10758420
    [Abstract] [Full Text] [Related]

  • 9. Progressive familial intrahepatic cholestasis.
    Cavestro GM, Frulloni L, Cerati E, Ribeiro LA, Corrente V, Sianesi M, Franzè A, Di Mario F.
    Acta Biomed; 2002 Mar 18; 73(3-4):53-6. PubMed ID: 12596388
    [Abstract] [Full Text] [Related]

  • 10. Progressive familial intrahepatic cholestasis and benign recurrent intrahepatic cholestasis: a review.
    Strubbe B, Geerts A, Van Vlierberghe H, Colle I.
    Acta Gastroenterol Belg; 2012 Dec 18; 75(4):405-10. PubMed ID: 23402083
    [Abstract] [Full Text] [Related]

  • 11. Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11.
    van Mil SW, van der Woerd WL, van der Brugge G, Sturm E, Jansen PL, Bull LN, van den Berg IE, Berger R, Houwen RH, Klomp LW.
    Gastroenterology; 2004 Aug 18; 127(2):379-84. PubMed ID: 15300568
    [Abstract] [Full Text] [Related]

  • 12. [Progressive familial intrahepatic cholestasis and hereditary anomalies lf hepatocellular metabolism of bile acids].
    Jacquemin E.
    Arch Pediatr; 1998 Jan 18; 5(1):45-53. PubMed ID: 10223112
    [Abstract] [Full Text] [Related]

  • 13. Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy.
    van der Woerd WL, van Mil SW, Stapelbroek JM, Klomp LW, van de Graaf SF, Houwen RH.
    Best Pract Res Clin Gastroenterol; 2010 Oct 18; 24(5):541-53. PubMed ID: 20955958
    [Abstract] [Full Text] [Related]

  • 14. [Recurrent benign intrahepatic cholestasis and their progression to familiar progressive intrahepatic cholestasis].
    Alburquerque Miranda M, Vargas Cárdenas G, Lozano Miranda Z, Reyes Mugruza T, Li Torres W, Valdivia Roldán M.
    Rev Gastroenterol Peru; 2008 Oct 18; 28(2):183-8. PubMed ID: 18641783
    [Abstract] [Full Text] [Related]

  • 15. Progressive familial intrahepatic cholestasis in Malaysian patients--a report of five cases.
    Lee WS, Chai PF, Looi LM.
    Med J Malaysia; 2009 Sep 18; 64(3):216-9. PubMed ID: 20527271
    [Abstract] [Full Text] [Related]

  • 16. Progressive familial intrahepatic cholestasis.
    Hori T, Nguyen JH, Uemoto S.
    Hepatobiliary Pancreat Dis Int; 2010 Dec 18; 9(6):570-8. PubMed ID: 21134824
    [Abstract] [Full Text] [Related]

  • 17. Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity.
    Haslam SI, Van Hul W, Morales-Piga A, Balemans W, San-Millan JL, Nakatsuka K, Willems P, Haites NE, Ralston SH.
    J Bone Miner Res; 1998 Jun 18; 13(6):911-7. PubMed ID: 9626621
    [Abstract] [Full Text] [Related]

  • 18. Benign recurrent intrahepatic cholestasis progressing to progressive familial intrahepatic cholestasis: low GGT cholestasis is a clinical continuum.
    van Ooteghem NA, Klomp LW, van Berge-Henegouwen GP, Houwen RH.
    J Hepatol; 2002 Mar 18; 36(3):439-43. PubMed ID: 11867191
    [Abstract] [Full Text] [Related]

  • 19. Genetics and Molecular Modeling of New Mutations of Familial Intrahepatic Cholestasis in a Single Italian Center.
    Giovannoni I, Callea F, Bellacchio E, Torre G, De Ville De Goyet J, Francalanci P.
    PLoS One; 2015 Mar 18; 10(12):e0145021. PubMed ID: 26678486
    [Abstract] [Full Text] [Related]

  • 20. Characterization of mutations in ATP8B1 associated with hereditary cholestasis.
    Klomp LW, Vargas JC, van Mil SW, Pawlikowska L, Strautnieks SS, van Eijk MJ, Juijn JA, Pabón-Peña C, Smith LB, DeYoung JA, Byrne JA, Gombert J, van der Brugge G, Berger R, Jankowska I, Pawlowska J, Villa E, Knisely AS, Thompson RJ, Freimer NB, Houwen RH, Bull LN.
    Hepatology; 2004 Jul 18; 40(1):27-38. PubMed ID: 15239083
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.