Atypical hemolytic uremic syndrome: From the rediscovery of complement to targeted therapy
Author:
Publisher
Elsevier BV
Subject
Internal Medicine
Reference13 articles.
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2. Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults;Fremeaux-Bacchi;Clin J Am Soc Nephrol,2013
3. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic–uremic syndrome;Furlan;N Engl J Med,1998
4. Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations;Fakhouri;J Am Soc Nephrol,2010
5. Thrombocytopenia is not mandatory to diagnose haemolytic and uremic syndrome;Sallee;BMC Nephrol,2013
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1. Recent Advances in the Management of Microangiopathic Hemolytic Anemias (MAHA): A Narrative Review;Cureus;2023-10-17
2. An ex vivo test to investigate genetic factors conferring susceptibility to atypical haemolytic uremic syndrome;Frontiers in Immunology;2023-02-09
3. Kidney diseases;Immunological Reviews;2022-11-12
4. Copy number variation analysis using next-generation sequencing identifies the CFHR3/CFHR1 deletion in atypical hemolytic uremic syndrome: a case report;Hematology;2022-05-26
5. Isolated thrombotic microangiopathy of the small intestine in a patient with atypical hemolytic uremic syndrome – a case report;BMC Nephrology;2020-03-24
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