Complement dysregulation in haemolytic uraemic syndrome
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference9 articles.
1. Long-term renal prognosis of diarrhea-associated hemolytic uremic syndrome: a systematic review, meta-analysis, and meta-regression;Garg;JAMA,2003
2. Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura;Ruggenenti;Kidney Int,2001
3. Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease;Caprioli;Hum Mol Genet,2003
4. Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome;Veyradier;J Pediatr,2003
5. Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome;Richards;Proc Natl Acad Sci USA,2003
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1. Thrombotic Thrombocytopenic Purpura and Related Thrombotic Microangiopathies;Consultative Hemostasis and Thrombosis;2019
2. Thrombotic Thrombocytopenic Purpura, Hemolytic-Uremic Syndrome, and HELLP;Critical Care Obstetrics;2018-10-05
3. NLRP3 is Required for Complement-Mediated Caspase-1 and IL-1beta Activation in ICH;Journal of Molecular Neuroscience;2016-12-08
4. Thrombotic Thrombocytopenic Purpura and Related Thrombotic Microangiopathies;Consultative Hemostasis and Thrombosis;2013
5. Thrombotic Thrombocytopenic Purpura, Hemolytic-Uremic Syndrome, and HELLP;Critical Care Obstetrics;2011-03-16
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