Literature DB >> 23889130

ADAMTS13 deficiency in severe postpartum HELLP syndrome.

Olivier Pourrat1, Rémi Coudroy, Fabrice Pierre.   

Abstract

Entities:  

Keywords:  HELLP syndrome; Haemolytic and Uraemic Syndrome; Plasma exchange; Thrombotic Thrombocytopenic Purpura; Thrombotic microangiopathy

Mesh：

Substances：

Year:  2013        PMID： 23889130     DOI： 10.1111/bjh.12494

Source DB:  PubMed          Journal:  Br J Haematol        ISSN： 0007-1048            Impact factor:   6.998


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  8 in total

Review 1.  Immunology of hepatic diseases during pregnancy.

Authors:  Lars Bremer; Christoph Schramm; Gisa Tiegs
Journal:  Semin Immunopathol       Date:  2016-06-20       Impact factor: 9.623

2.  Severe reduction of free-form ADAMTS13, unbound to von Willebrand factor, in plasma of patients with HELLP syndrome.

Authors:  Yoko Yoshida; Masanori Matsumoto; Hideo Yagi; Ayami Isonishi; Kazuya Sakai; Masaki Hayakawa; Yuji Hori; Toshiyuki Sado; Hiroshi Kobayashi; Yoshihiro Fujimura
Journal:  Blood Adv       Date:  2017-08-23

3.  Clinical and renal biopsy findings predicting outcome in renal thrombotic microangiopathy: a large cohort study from a single institute in China.

Authors:  Xiao-Juan Yu; Feng Yu; Di Song; Su-Xia Wang; Yan Song; Gang Liu; Ming-Hui Zhao
Journal:  ScientificWorldJournal       Date:  2014-08-11

Review 4.  TTP-like syndrome: novel concept and molecular pathogenesis of endotheliopathy-associated vascular microthrombotic disease.

Authors:  Jae C Chang
Journal:  Thromb J       Date:  2018-08-11

5.  Severe HELLP syndrome masquerading as thrombocytopenic thrombotic purpura: a case report.

Authors:  Cyril Mousseaux; Bérangère S Joly; Inna Mohamadou; Romain Arrestier; Alexandre Hertig; Cédric Rafat
Journal:  BMC Nephrol       Date:  2020-05-29       Impact factor: 2.388

6.  Acute Respiratory Distress Syndrome as an Organ Phenotype of Vascular Microthrombotic Disease: Based on Hemostatic Theory and Endothelial Molecular Pathogenesis.

Authors:  Jae C Chang
Journal:  Clin Appl Thromb Hemost       Date:  2019 Jan-Dec       Impact factor: 2.389

7.  HELLP Syndrome, Thrombotic Thrombocytopenic Purpura or Both: Appraising the Complex Association and Proposing a Stepwise Practical Plan for Differential Diagnosis.

Authors:  Mohamad K Ramadan; Dominique A Badr; Manal Hubeish; Saadeddine Itani; Haneen Hijazi; Anas Mogharbil
Journal:  J Hematol (Brossard)       Date:  2017-01-10

Review 8.  Platelet Activation Mechanisms and Consequences of Immune Thrombocytopenia.

Authors:  Siyu Sun; Rolf T Urbanus; Hugo Ten Cate; Philip G de Groot; Bas de Laat; Johan W M Heemskerk; Mark Roest
Journal:  Cells       Date:  2021-12-01       Impact factor: 6.600
  8 in total

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