ADAMTS13 deficiency in severe postpartum HELLP syndrome-Reference-Cited by-同舟云学术

ADAMTS13 deficiency in severe postpartum HELLP syndrome

Published:2013-07-24 Issue:3 Volume:163 Page:409-410
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Pourrat Olivier,Coudroy Rémi¹,Pierre Fabrice²

Affiliation:

1. Intensive Care and Internal Medicine Unit; University of Poitiers; Poitiers; France

2. Department of Gynaecology and Obstetrics; University of Poitiers; Poitiers; France

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.12494/fullpdf

Reference9 articles.

1. How I treat patients with thrombotic thrombocytopenic purpura: 2010;George;Blood,2010

2. A high LDH to AST ratio helps to differentiate pregnancy-associated thrombotic thrombocytopenic purpura (TTP) from HELLP syndrome;Keiser;Journal of Maternal Fetal and Neonatal Medicine,2012

3. Mild to moderate reduction of a von Willebrand factor cleaving protease (ADAMTS-13) in pregnant women with HELLP microangiopathic syndrome;Lattuada;Haematologica,2003

4. Imitators of preeclampsia and HELLP syndrome;Martin;Obstetrics and Gynecology Clinics of North America,1991

5. Plasma exchange for preeclampsia. I. Postpartum use for persistently severe preeclampsia-eclampsia with HELLP syndrome;Martin;American Journal of Obstetrics and Gynecology,1990

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