Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome
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Atypical hemolytic uremic syndromeClinical Practice Guidelines for the Management of Atypical Hemolytic Uremic Syndrome in KoreaAdvances and challenges in the management of complement-mediated thrombotic microangiopathiesCurrent treatment of atypical hemolytic uremic syndromeComplement regulator CD46: genetic variants and disease associationsGenetics and complement in atypical HUS.Do complement factor H 402Y and C7 M allotypes predispose to (typical) haemolytic uraemic syndrome?Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP.Age-related penetrance of hereditary atypical hemolytic uremic syndrome.Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?Thrombotic microangiopathy and associated renal disorders.Familial atypical hemolytic uremic syndrome: a review of its genetic and clinical aspects.Multifaceted hemolytic uremic syndrome in pediatrics.Complement therapy in atypical haemolytic uraemic syndrome (aHUS).Dynamics of complement activation in aHUS and how to monitor eculizumab therapyAtypical 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.The role of ADAMTS-13 activity and complement mutational analysis in differentiating acute thrombotic microangiopathiesReview: Complement and its regulatory proteins in kidney diseases.Guidelines on the use of therapeutic apheresis in clinical practice--evidence-based approach from the Apheresis Applications Committee of the American Society for Apheresis.Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levelsComplement Dysregulation and Disease: Insights from Contemporary Genetics.Update on hemolytic uremic syndrome: Diagnostic and therapeutic recommendations.Atypical hemolytic uremic syndrome: a clinical conundrum.Atypical hemolytic uremic syndromeHemolytic uremic syndrome
P2860
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P2860
Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին 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
Epidemiological approach to id ...... ical hemolytic uremic syndrome
@ast
Epidemiological approach to id ...... ical hemolytic uremic syndrome
@en
Epidemiological approach to id ...... ical hemolytic uremic syndrome
@nl
type
label
Epidemiological approach to id ...... ical hemolytic uremic syndrome
@ast
Epidemiological approach to id ...... ical hemolytic uremic syndrome
@en
Epidemiological approach to id ...... ical hemolytic uremic syndrome
@nl
prefLabel
Epidemiological approach to id ...... ical hemolytic uremic syndrome
@ast
Epidemiological approach to id ...... ical hemolytic uremic syndrome
@en
Epidemiological approach to id ...... ical hemolytic uremic syndrome
@nl
P2093
P3181
P1476
Epidemiological approach to id ...... ical hemolytic uremic syndrome
@en
P2093
Andreas Bock
Bernd Hoppe
Gani Berisha
Hartmut P H Neumann
Karl Lhotta
Klaus Arbeiter
Klemens Budde
Lisa A Rybicki
Ludwig Patzer
Maren Sullivan
P3181
P356
10.1111/J.1469-1809.2009.00554.X
P407
P577
2010-01-01T00:00:00Z