Genetic and molecular evidence for complement dysregulation in patients with HELLP syndrome-Reference-Cited by-同舟云学术

Genetic and molecular evidence for complement dysregulation in patients with HELLP syndrome

Published:2020-12 Issue: Volume:196 Page:167-174
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Bazzan Mario,Todros Tullia,Tedeschi Silvana,Ardissino Gianluigi,Cardaropoli Simona,Stella Stefania,Montaruli Barbara,Marchese Cristiana,Roccatello Dario,Cugno Massimo^ORCID

Funder

Alexion Pharma Inc.

Publisher

Elsevier BV

Subject

Hematology

Reference53 articles.

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5. Prognostic factors of the efficacy of high-dose corticosteroid therapy in hemolysis, elevated liver enzymes, and low platelet count syndrome during pregnancy: a meta-analysis;Yang;Medicine (Baltimore),2016

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1. Possibilities of Predicting the Manifestation of HELLP Syndrome;Ural Medical Journal;2024-07-12

2. Le HELLP syndrome dans tous ses états;Revue Francophone des Laboratoires;2024-03

3. Serum protein profile analysis via label-free quantitation proteomics in patients with early-onset preeclampsia;Journal of Obstetrics and Gynaecology;2023-09-24

4. Complement biology for hematologists;American Journal of Hematology;2023-03-31

5. Evaluation of long noncoding RNA (LncRNA) in pathogenesis of HELLP syndrome: diagnostic and future approach;Journal of Obstetrics and Gynaecology;2023-02-16