On the relevance of thrombomodulin variants in atypical hemolytic uremic syndrome-Reference-Cited by-同舟云学术

On the relevance of thrombomodulin variants in atypical hemolytic uremic syndrome

Published:2023-10 Issue:4 Volume:104 Page:851-855
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Huerta Ana^ORCID,Arjona Emi,Portoles Jose,Lopez-Sanchez Paula,Cavero Teresa^ORCID,Fernandez-Cusicanqui Jeanette,Blasco Miquel,Cabello Virginia,Calvo Natividad,Diaz Montserrat,Herrero-Goñi Maria,Aguirre Mireia,Elías Sandra,Alcaide Maria Paz,Ramos Natalia,Sellares Joana,Rodríguez de Córdoba Santiago

Publisher

Elsevier BV

Subject

Nephrology

Reference9 articles.

1. Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference;Goodship;Kidney Int,2017

2. Thrombotic microangiopathy in aHUS and beyond: clinical clues from complement genetics;Fakhouri;Nat Rev Nephrol,2021

3. How I diagnose and treat atypical hemolytic uremic syndrome;Fakhouri;Blood,2023

4. Thrombomodulin mutations in atypical hemolytic-uremic syndrome;Delvaeye;N Engl J Med,2009

5. Thrombomodulin enhances complement regulation through strong affinity interactions with factor H and C3b-factor H complex;Heurich;Thromb Res,2016

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Successful 13‐year ongoing remission with C5 inhibitor therapy following renal transplant in atypical hemolytic uremic syndrome;American Journal of Hematology;2024-08-23

2. Recurrent complement-mediated Hemolytic uremic syndrome after kidney transplantation;Transplantation Reviews;2024-07