Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS)
about
Atypical hemolytic uremic syndromeStructural basis for complement factor I control and its disease-associated sequence polymorphismsClinical Practice Guidelines for the Management of Atypical Hemolytic Uremic Syndrome in KoreaAdvances and challenges in the management of complement-mediated thrombotic microangiopathiesComplement regulator CD46: genetic variants and disease associationsGenetics and complement in atypical HUS.Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP.Immunogenicity of meningococcus C vaccination in a patient with atypical hemolytic uremic syndrome (aHUS) on eculizumab therapy.Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristicsAtypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 geneNovel C3 mutation p.Lys65Gln in aHUS affects complement factor H binding.Thrombotic microangiopathy and associated renal disorders.Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults.Complement therapy in atypical haemolytic uraemic syndrome (aHUS).Complement factor B mutations in atypical hemolytic uremic syndrome-disease-relevant or benign?Complement activation patterns in atypical haemolytic uraemic syndrome during acute phase and in remission.Novel aspects of atypical haemolytic uraemic syndrome and the role of eculizumab.Atypical haemolytic uraemic syndrome treated with the complement inhibitor eculizumab: the experience of the Australian compassionate access cohort.Incomplete penetrance of CD46 mutation causing familial atypical hemolytic uremic syndrome.Recovery of renal function after long-term dialysis and resolution of cardiomyopathy in a patient with aHUS receiving eculizumab.Anti-complement-factor H-associated glomerulopathies.Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levelsWhere genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.Update on hemolytic uremic syndrome: Diagnostic and therapeutic recommendations.Adjustment of Eculizumab Dosage Pattern in Patients with Atypical Hemolytic Uremic Syndrome with Suboptimal Response to Standard Treatment Pattern.Serological and genetic complement alterations in infection-induced and complement-mediated hemolytic uremic syndrome.Hemolytic Uremic Syndrome in Pregnancy and Postpartum.Complete factor I deficiency due to dysfunctional factor I with recurrent aseptic meningo-encephalitis.Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family.Overactivity of Alternative Pathway Convertases in Patients With Complement-Mediated Renal Diseases.Characterization of genetic predisposition and autoantibody profile in atypical haemolytic-uraemic syndrome.The clinical and laboratory features of Chinese Han anti-factor H autoantibody-associated hemolytic uremic syndrome.Atypical hemolytic uremic syndrome
P2860
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P2860
Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS)
description
2010 nî lūn-bûn
@nan
2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Genetic disorders in complemen ...... olytic uraemic syndrome (aHUS)
@ast
Genetic disorders in complemen ...... olytic uraemic syndrome (aHUS)
@en
Genetic disorders in complemen ...... olytic uraemic syndrome (aHUS)
@nl
type
label
Genetic disorders in complemen ...... olytic uraemic syndrome (aHUS)
@ast
Genetic disorders in complemen ...... olytic uraemic syndrome (aHUS)
@en
Genetic disorders in complemen ...... olytic uraemic syndrome (aHUS)
@nl
prefLabel
Genetic disorders in complemen ...... olytic uraemic syndrome (aHUS)
@ast
Genetic disorders in complemen ...... olytic uraemic syndrome (aHUS)
@en
Genetic disorders in complemen ...... olytic uraemic syndrome (aHUS)
@nl
P2093
P3181
P356
P1476
Genetic disorders in complemen ...... olytic uraemic syndrome (aHUS)
@en
P2093
Annemieke Vos
Dineke Westra
Edwin van Kaauwen
Eefje van der Heijden
Jitske Jansen
Lambert van den Heuvel
Marleen Huigen
Nicole van de Kar
Thea van der Velden
P304
P3181
P356
10.1093/NDT/GFQ010
P407
P577
2010-07-01T00:00:00Z