Use of Highly Individualized Complement Blockade Has Revolutionized Clinical Outcomes after Kidney Transplantation and Renal Epidemiology of Atypical Hemolytic Uremic Syndrome
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Title
Use of Highly Individualized Complement Blockade Has Revolutionized Clinical Outcomes after Kidney Transplantation and Renal Epidemiology of Atypical Hemolytic Uremic Syndrome
Authors
Keywords
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Journal
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
Volume -, Issue -, Pages ASN.2019040331
Publisher
American Society of Nephrology (ASN)
Online
2019-10-02
DOI
10.1681/asn.2019040331
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Note: Only part of the references are listed.- Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference
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- Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome
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- (2013) Julien Zuber et al. Transplantation Reviews
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- Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies
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- Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype
- (2010) M. Noris et al. Clinical Journal of the American Society of Nephrology
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- (2010) Julien Zuber et al. Nature Reviews Nephrology
- Anti-Factor H Autoantibodies in a Fifth Renal Transplant Recipient with Atypical Hemolytic and Uremic Syndrome
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