Concurrent Atypical Hemolytic Uremic Syndrome and Autoimmune Hemolytic Anemia: a case report
Background: Atypical hemolytic uremic syndrome (aHUS) is a life-threatening and scarce disorder characterized by acute renal failure and disease, non-immune microangiopathic hemolytic anemia and thrombocytopenia, leading to end-stage renal failure or ...
Sayed Yousef Mojtahedi+1 more
doaj
Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome [PDF]
Elena Goicoechea de Jorge+9 more
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Intravenous gamma globulin for atypical hemolytic uremic syndrome [PDF]
Shuichi Ito+2 more
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A Novel Non-Synonymous Polymorphism (p.Arg240His) in C4b-Binding Protein Is Associated with Atypical Hemolytic Uremic Syndrome and Leads to Impaired Alternative Pathway Cofactor Activity [PDF]
Anna M. Blom+14 more
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Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation [PDF]
Anne-lie Ståhl+9 more
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Hemolytic-uremic syndrome in Switzerland: a nationwide surveillance 1997-2003 [PDF]
Hemolytic-uremic syndrome (HUS) is a leading cause of acute renal failure in childhood. In its typical presentation, it is preceded by an episode of diarrhea mostly due to Shiga-toxin-producing Escherichia coli.
Bianchetti, Mario+6 more
core
Eculizumab for Congenital Atypical Hemolytic–Uremic Syndrome [PDF]
Ralph A. Gruppo, Russell P. Rother
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