Posttransplantation cytomegalovirus-induced recurrence of atypical hemolytic uremic syndrome associated with a factor H mutation: Successful treatment with intensive plasma exchanges and ganciclovir
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference27 articles.
1. Recurrence of haemolytic-uraemic syndrome in renal transplants;Miller;Nephrol Dial Transplant,1997
2. Post-transplant haemolytic uremic syndrome;Ruggenenti;Kidney Int,2002
3. Genetic studies into inherited and sporadic hemolytic uremic syndrome;Warwicker;Kidney Int,1998
4. Familial hemolytic uremic syndrome associated with complement factor H deficiency;Landau;J Pediatr,2000
5. Von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and haemolytic uremic syndrome;Remuzzi;Blood,2002
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1. Early graft loss due to acute thrombotic microangiopathy accompanied by complement gene variants in living-related kidney transplantation: case series report;BMC Nephrology;2022-07-14
2. Concurrent cytomegalovirus enteritis and atypical hemolytic uremic syndrome with gastrointestinal tract involvement: a case report;Korean Journal of Transplantation;2021-12-31
3. De Novo and Recurrent Thrombotic Microangiopathy After Renal Transplantation: Current Concepts in Management;Experimental and Clinical Transplantation;2021-09-20
4. Familial atypical hemolytic uremic syndrome with positive p.S1191L (c.3572C>T) mutation on the CFH gene: A single-center experience;Balkan Journal of Medical Genetics;2021-06-01
5. Thrombotic Microangiopathy After Kidney Transplantation: An Underdiagnosed and Potentially Reversible Entity;Frontiers in Medicine;2021-04-08
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