Systematic review of atypical hemolytic uremic syndrome biomarkers | SpringerLink
Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I - Nilsson - 2010 - European Journal of Immunology - Wiley Online Library
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June 2020 — Molecular Pathology - Insights
Optimal management of atypical hemolytic uremic disease: challenges and solutions. - Document - Gale Academic OneFile
Thrombotic microangiopathy after renal transplantation: Current insights in de novo and recurrent disease. - Abstract - Europe PMC
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Optimal management of atypical hemolytic uremic disease: challenges and solutions. - Document - Gale Academic OneFile
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Anti-Factor H Antibody Reactivity in Young Adults Vaccinated with a Meningococcal Serogroup B Vaccine Containing Factor H Binding Protein | mSphere
Thrombotic microangiopathy after renal transplantation: Current insights in de novo and recurrent disease
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Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference - Kidney International
Mutations of Factor H Impair Regulation of Surface-bound C3b by Three Mechanisms in Atypical Hemolytic Uremic Syndrome - ScienceDirect
Frontiers | The Relevance of the MCP Risk Polymorphism to the Outcome of aHUS Associated With C3 Mutations. A Case Report | Immunology
Thrombotic microangiopathy after renal transplantation: Current insights in de novo and recurrent disease. - Abstract - Europe PMC
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference - Kidney International
Complement, inflammation and thrombosis - Rawish - 2021 - British Journal of Pharmacology - Wiley Online Library
Genetic analysis in the patients with aHUS included in group 1. (A)... | Download Scientific Diagram
Direct evidence of complement activation in HELLP syndrome: A link to atypical hemolytic uremic syndrome - Experimental Hematology
The Major Autoantibody Epitope on Factor H in Atypical Hemolytic Uremic Syndrome Is Structurally Different from Its Homologous Site in Factor H-related Protein 1, Supporting a Novel Model for Induction of Autoimmunity
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Distribution of rare missense or truncating variants in CFI included in... | Download Scientific Diagram
Thrombotic microangiopathy after renal transplantation: Current insights in de novo and recurrent disease. - Abstract - Europe PMC
An extended mini-complement factor H molecule ameliorates experimental C3 glomerulopathy - ScienceDirect
Frontiers | The Relevance of the MCP Risk Polymorphism to the Outcome of aHUS Associated With C3 Mutations. A Case Report | Immunology
