共 9 条
[1]
[2]
胆汁瘀积性肝病发病的分子学进展[J] 任可;徐灿;金震东;李兆申; 世界华人消化杂志 2001,
[3]
BSEP基因突变在低γ-GT的进行性肝内胆汁淤积中的意义[A] 王中林;朱启镕;王建设;王晓红; 中华医学会第十四次全国儿科学术会议 2006,
[4]
Altered hepatobiliary gene expressions in PFIC1: ATP8B1 gene defect is associated with CFTR downregulation[J] Christine Demeilliers;Emmanuel Jacquemin;Véronique Barbu;Martine Mergey;Fran?ois Paye;Laura Fouassier;Nicolas Chignard;Chantal Housset;Nour‐Eddine Lomri Hepatology 2006,
[5]
Progressive familial intrahepatic cholestasis; type 1; is associated with decreased farnesoid X receptor activity[J] Frank Chen;M. Ananthanarayanan;Sukru Emre;Ezequiel Neimark;Laura N. Bull;A.S. Knisely;Sandra S. Strautnieks;Richard J. Thompson;Margret S. Magid;Ronald Gordon;N. Balasubramanian;Frederick J. Suchy;Benjamin L. Shneider Gastroenterology 2004,
[6]
Biliary diversion for progressive familial intrahepatic cholestasis: improved liver morphology and bile acid profile[J] Amethyst C Kurbegov;Kenneth D.R Setchell;Joel E Haas;Gary W Mierau;Michael Narkewicz;John D Bancroft;Frederick Karrer;Ronald J Sokol Gastroenterology 2003,
[7]
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[J] Panayotis Lykavieris;Saskia van Mil;Danièle Cresteil;Monique Fabre;Michelle Hadchouel;Leo Klomp;Olivier Bernard;Emmanuel Jacquemin Journal of Hepatology 2003,
[8]
Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis[J] Gastroenterology 1999,
[9]
Defect of multidrug-resistance 3 gene expression in a subtype of progressive familial intrahepatic cholestasis[J] J Deleuze;E Jacquemin;C Dubuisson;D Cresteil;M Dumont;S Erlinger;O Bernard;M Hadchouel Hepatology 1996,