Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
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Complement factor H gene associations with end-stage kidney disease in African Americans.Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome.Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognitionNew aspects in the pathogenesis and treatment of thrombotic thrombocytopenic purpura and hemolytic uremic syndrome.Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countriesMutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome.Familial mesangio-capillary glomerulonephritis with initial presentation as haemolytic uraemic syndrome.Factor H binds to washed human platelets.Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutation.Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals.Familial atypical hemolytic uremic syndrome: a review of its genetic and clinical aspects.Eculizumab in neonatal hemolytic uremic syndrome with homozygous factor H deficiency.Complement control protein factor H: the good, the bad, and the inadequate.Molecular basis of autosomal recessive diseases among the Palestinian Arabs.Mesenchymal stem cells inhibit complement activation by secreting factor H.Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy.The Genetics of Ultra-Rare Renal Disease.Serum cystatin C level, kidney disease markers, and incidence of age-related macular degeneration: the Beaver Dam Eye Study.New functional and structural insights from updated mutational databases for complement factor H, Factor I, membrane cofactor protein and C3.Complement factor H in host defense and immune evasion.Idiopathic Atypical Hemolytic Uremic Syndrome (aHUS) with Trilineage Myelodysplasia.Complement factor H in AMD: Bridging genetic associations and pathobiology.Reply to buddles et al.Atypical hemolytic-uremic syndrome due to complement factor I mutation.Proteomics in Ménière disease.Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family.Determination of complement factor H functional polymorphisms (V62I, Y402H, and E936D) using sequence-specific primer PCR and restriction fragment length polymorphisms.Concomitant anuric post-streptococcal glomerulonephritis and autoimmune hemolytic anemia
P2860
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P2860
Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.
description
1999 nî lūn-bûn
@nan
1999 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Complement factor H gene mutat ...... cal hemolytic uremic syndrome.
@ast
Complement factor H gene mutat ...... cal hemolytic uremic syndrome.
@en
Complement factor H gene mutat ...... cal hemolytic uremic syndrome.
@nl
type
label
Complement factor H gene mutat ...... cal hemolytic uremic syndrome.
@ast
Complement factor H gene mutat ...... cal hemolytic uremic syndrome.
@en
Complement factor H gene mutat ...... cal hemolytic uremic syndrome.
@nl
prefLabel
Complement factor H gene mutat ...... cal hemolytic uremic syndrome.
@ast
Complement factor H gene mutat ...... cal hemolytic uremic syndrome.
@en
Complement factor H gene mutat ...... cal hemolytic uremic syndrome.
@nl
P2093
P2860
P356
P1476
Complement factor H gene mutat ...... cal hemolytic uremic syndrome.
@en
P2093
Schlesinger M
Sheffield VC
P2860
P304
P356
10.1086/302673
P407
P577
1999-12-01T00:00:00Z