Ex Vivo Test of Complement Dysregulation in Atypical Hemolytic Uremic Syndrome Kidney Transplant patients: A Pilot Study
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference17 articles.
1. Anticomplement treatment in atypical and typical hemolytic uremic syndrome;Fakhouri;Semin Hematol,2018
2. Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome;Le Quintrec;Am J Transplant,2013
3. Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference;Goodship;Kidney Int,2017
4. Eculizumab rescue therapy in patients with recurrent atypical hemolytic uremic syndrome after kidney transplantation;Duineveld;Kidney Int Rep,2023
5. Use of highly individualized complement blockade has revolutionized clinical outcomes after kidney transplantation and renal epidemiology of atypical hemolytic uremic syndrome;Zuber;J Am Soc Nephrol,2019
Cited by 3 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. Exuberant Endothelial C5b-9 Formation in Recurrent and De Novo Posttransplant Thrombotic Microangiopathy;Kidney International Reports;2024-08
2. Ex vivo C5b-9 Deposition Test to Monitor Complement Activity in Clinical and Subclinical Atypical Hemolytic Uremic Syndrome and in Transplantation-Associated Thrombotic Microangiopathy;Kidney International Reports;2024-07
3. A Caution Against the Use of C5b-9 Endothelial Assay to Support Eculizumab Therapy: A response to Maritati et al.: “Eculizumab first” in the management of posttransplant thrombotic microangiopathy;Kidney International Reports;2024-05
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