Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopeni

Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopeni

Item
http://www.wikidata.org/entity/Q33328553
Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcomeHemolytic uremic syndrome: toxins, vessels, and inflammationThe interaction between factor H and Von Willebrand factor.Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognitionMutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.Mannan-binding lectin in children with Escherichia coli O157:H7 haemmorrhagic colitis and haemolytic uraemic syndrome.Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countriesModeling how CD46 deficiency predisposes to atypical hemolytic uremic syndromeSuccessful split liver-kidney transplant for factor H associated hemolytic uremic syndrome.Complement activation in thrombotic microangiopathiesComplement activation associated with ADAMTS13 deficiency in human and murine thrombotic microangiopathyThrombotic microangiopathy in haematopoietic cell transplantation: an update.Annexin A2 Enhances Complement Activation by Inhibiting Factor HThe burden of genetic disease on inpatient care in a children's hospital.Cutaneous Vasculitis and Digital Ischaemia Caused by Heterozygous Gain-of-Function Mutation in
P2860

Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopeni

Item
http://www.wikidata.org/entity/Q33328553
description
1999 nî lūn-bûn
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1999 թուականի Փետրուարին հրատարակուած գիտական յօդուած
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1999 թվականի փետրվարին հրատարակված գիտական հոդված
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1999年の論文
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Hypocomplementemia discloses g ...... ome/Thrombotic Thrombocytopeni
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