Literature DB >> 11596624

Thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: diagnosis and treatment.

J N George1, S K Vesely.   

Abstract

Prompt recognition of thrombotic thrombocytopenic purpura-hemolytic uremic syndrome (TTP-HUS) and initiation of plasma exchange treatment is critical as it substantially decreases mortality. Nevertheless, death and long-term complications remain common. The recent relaxation of diagnostic criteria has dramatically increased the number of patients treated for clinically suspected TTP-HUS.

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Year:  2001        PMID: 11596624     DOI: 10.3949/ccjm.68.10.857

Source DB:  PubMed          Journal:  Cleve Clin J Med        ISSN: 0891-1150            Impact factor:   2.321


  4 in total

1.  A leptospirosis case presenting with thrombotic thrombocytopenic purpura.

Authors:  Köse Sükran; Bengü Tatar; Gürsel Ersan; Selim Topaloğlu
Journal:  Balkan Med J       Date:  2013-12-01       Impact factor: 2.021

2.  Quinine allergy causing acute severe systemic illness: report of 4 patients manifesting multiple hematologic, renal, and hepatic abnormalities.

Authors:  Mark A Howard; Andrea B Hibbard; Deirdra R Terrell; Patrick J Medina; Sara K Vesely; James N George
Journal:  Proc (Bayl Univ Med Cent)       Date:  2003-01

Review 3.  ADAMTS13 conformations and mechanism of inhibition in immune thrombotic thrombocytopenic purpura.

Authors:  Konstantine Halkidis; X Long Zheng
Journal:  J Thromb Haemost       Date:  2022-08-03       Impact factor: 16.036

4.  Management of Shiga toxin-associated Escherichia coli-induced haemolytic uraemic syndrome: randomized clinical trials are needed.

Authors:  Diana Karpman
Journal:  Nephrol Dial Transplant       Date:  2012-10       Impact factor: 5.992

  4 in total

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