Literature DB >> 3441786

Familial primary biliary cirrhosis and autoimmune thrombocytopenia.

E A Chalmers1, D Chan Lam, R J Holden, E J Fitzimons.   

Abstract

Primary biliary cirrhosis (PBC) is described in two sisters, one of whom presented with autoimmune thrombocytopenia. Taken together with reports of platelet autoantibodies in PBC this case may indicate a place for immunosuppressive agents in the treatment of thrombocytopenia in PBC.

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Year:  1987        PMID： 3441786     DOI： 10.1177/003693308703200512

Source DB:  PubMed          Journal:  Scott Med J        ISSN： 0036-9330            Impact factor:   0.729


  3 in total

Review 1.  Prevalence and pattern of familial disease in primary biliary cirrhosis.

Authors:  A M Brind; G P Bray; B C Portmann; R Williams
Journal:  Gut       Date:  1995-04       Impact factor: 23.059

2.  Familial clustering and genetic background of primary biliary cirrhosis in Japan.

Authors:  Masatoshi Yanagisawa; Hitoshi Takagi; Hitomi Takahashi; Masahiro Uehara; Toshiyuki Otsuka; Kazuhisa Yuasa; Kenichi Hosonuma; Masatomo Mori
Journal:  Dig Dis Sci       Date:  2009-12-11       Impact factor: 3.199

3.  Primary biliary cirrhosis associated with idiopathic thrombocytopenic purpura.

Authors:  Y Mizukami; M Ohhira; A Matsumoto; Y Murazumi; K Murazumi; H Ohta; M Ohhira; M Ono; T Miyake; I Maekawa; Y Kohgo
Journal:  J Gastroenterol       Date:  1996-04       Impact factor: 7.527
  3 in total

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