Pages that link to "Q64449254"
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The following pages link to Atypical hemolytic uremic syndrome (Q64449254):
Displaying 17 items.
- Dual interaction of factor H with C3d and glycosaminoglycans in host-nonhost discrimination by complement (Q24619612) (← links)
- The interaction between factor H and Von Willebrand factor (Q31133820) (← links)
- Novel C3 mutation p.Lys65Gln in aHUS affects complement factor H binding (Q33401619) (← links)
- Complement activation in thrombotic microangiopathies (Q33404158) (← links)
- Complement disorders and hemolytic uremic syndrome (Q33405802) (← links)
- Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype (Q33406025) (← links)
- Complement and cytokine response in acute Thrombotic Thrombocytopenic Purpura (Q33412347) (← links)
- An audit analysis of a guideline for the investigation and initial therapy of diarrhea negative (atypical) hemolytic uremic syndrome (Q33415218) (← links)
- A novel atypical hemolytic uremic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation (Q33415753) (← links)
- Complement activation patterns in atypical haemolytic uraemic syndrome during acute phase and in remission (Q33416830) (← links)
- Advances in differential diagnosis and treatment of thrombotic microangiopathy (Q33421811) (← links)
- Efficacy and safety of eculizumab in adult patients with atypical hemolytic uremic syndrome: A single center experience from Turkey (Q33436018) (← links)
- Current status in diagnosis and treatment of hereditary thrombotic thrombocytopenic purpura. (Q34377532) (← links)
- New combined CFH/MCP mutations and a rare clinical course in atypical haemolytic uraemic syndrome (Q36306787) (← links)
- Reversal of threatening blindness after initiation of eculizumab in Purtscher-like retinopathy secondary to atypical hemolytic uremic syndrome. (Q48147152) (← links)
- C3 Glomerulopathy and Atypical Hemolytic Uremic Syndrome: Two Important Manifestations of Complement System Dysfunction. (Q55287167) (← links)
- Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS (Q64039246) (← links)