Functional evaluation of factor H genetic and acquired abnormalities: application for atypical hemolytic uremic syndrome (aHUS).
about
Complement factor B mutations in atypical hemolytic uremic syndrome-disease-relevant or benign?A novel quantitative hemolytic assay coupled with restriction fragment length polymorphisms analysis enabled early diagnosis of atypical hemolytic uremic syndrome and identified unique predisposing mutations in Japan.Clinical characteristics of children with hemolytic uremic syndrome in Hangzhou, China.Complement System Part I - Molecular Mechanisms of Activation and Regulation.A Familial C3GN Secondary to Defective C3 Regulation by Complement Receptor 1 and Complement Factor HEndothelial cells: source, barrier, and target of defensive mediators.
P2860
Functional evaluation of factor H genetic and acquired abnormalities: application for atypical hemolytic uremic syndrome (aHUS).
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Functional evaluation of facto ...... olytic uremic syndrome (aHUS).
@ast
Functional evaluation of facto ...... olytic uremic syndrome (aHUS).
@en
type
label
Functional evaluation of facto ...... olytic uremic syndrome (aHUS).
@ast
Functional evaluation of facto ...... olytic uremic syndrome (aHUS).
@en
prefLabel
Functional evaluation of facto ...... olytic uremic syndrome (aHUS).
@ast
Functional evaluation of facto ...... olytic uremic syndrome (aHUS).
@en
P2093
P50
P1476
Functional evaluation of facto ...... olytic uremic syndrome (aHUS).
@en
P2093
Caroline Blanc
Nelly Poulain
Roxane Roquigny
Stéphanie Ngo
Véronique Frémeaux-Bacchi
P304
P356
10.1007/978-1-62703-724-2_19
P407
P577
2014-01-01T00:00:00Z