Complement factor H and the haemolytic uraemic syndrome.
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Pathogenesis of thrombotic microangiopathiesIs severe deficiency of ADAMTS-13 specific for thrombotic thrombocytopenic purpura? YesMutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countriesFactor H binds to washed human platelets.The molecular basis for hereditary porcine membranoproliferative glomerulonephritis type II: point mutations in the factor H coding sequence block protein secretion.Role of Factor H and Related Proteins in Regulating Complement Activation in the Macula, and Relevance to Age-Related Macular Degeneration.Kidney Transplantation in Patients with Atypical Hemolytic Uremic Syndrome due to Complement Factor H Deficiency: Impact of Liver Transplantation.
P2860
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P2860
Complement factor H and the haemolytic uraemic syndrome.
description
2001 nî lūn-bûn
@nan
2001 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Complement factor H and the haemolytic uraemic syndrome.
@ast
Complement factor H and the haemolytic uraemic syndrome.
@en
Complement factor H and the haemolytic uraemic syndrome.
@nl
type
label
Complement factor H and the haemolytic uraemic syndrome.
@ast
Complement factor H and the haemolytic uraemic syndrome.
@en
Complement factor H and the haemolytic uraemic syndrome.
@nl
prefLabel
Complement factor H and the haemolytic uraemic syndrome.
@ast
Complement factor H and the haemolytic uraemic syndrome.
@en
Complement factor H and the haemolytic uraemic syndrome.
@nl
P1433
P1476
Complement factor H and the haemolytic uraemic syndrome.
@en
P2093
C M Taylor
P304
P356
10.1016/S0140-6736(01)06339-5
P407
P577
2001-10-01T00:00:00Z