Familial hemolytic-uremic syndrome and homozygous factor H deficiency.
about
Atypical hemolytic uremic syndromeHuman factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolismPathogenesis of thrombotic microangiopathiesHeterogeneity of atypical haemolytic uraemic syndromesComplement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.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 recognitionThrombotic microangiopathies in bone marrow and organ transplant patients.Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndromeRecurrent hemolytic uremic syndrome.Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countriesFamilial mesangio-capillary glomerulonephritis with initial presentation as haemolytic uraemic syndrome.Factor H binds to washed human platelets.Atypical haemolytic uraemic syndrome and mutations in complement regulator genes.Two generations with familial thrombotic thrombocytopenic purpura.Ocular involvement in hemolytic uremic syndrome due to factor H deficiency--are there therapeutic consequences?Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H.Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals.Hemolytic uremic syndrome due to homozygous factor H deficiency.aHUS caused by complement dysregulation: new therapies on the horizon.Advances in understanding the aetiology of atypical Haemolytic Uraemic Syndrome.Complement control protein factor H: the good, the bad, and the inadequate.Kidney function, albuminuria and age-related macular degeneration in NHANES III.The molecular basis for hereditary porcine membranoproliferative glomerulonephritis type II: point mutations in the factor H coding sequence block protein secretion.Acute presentation and persistent glomerulonephritis following streptococcal infection in a patient with heterozygous complement factor H-related protein 5 deficiency.Clinical aspects and molecular basis of primary deficiencies of complement component C3 and its regulatory proteins factor I and factor H.Genetic kidney diseases in the pediatric population of southern Israel.Approach to the patient with recurrent infections.Polyanion-induced self-association of complement factor H.Post-infectious Proliferative Glomerulonephritis with Monoclonal Immunoglobulin G Deposits Associated with Complement Factor H Mutation.Disruption of disulfide bonds is responsible for impaired secretion in human complement factor H deficiency.From humoral rejection to generalized thrombotic microangiopathy--role of acquired ADAMTS13 deficiency in a renal allograft recipient.The role of von Willebrand factor in thrombotic microangiopathy.Thrombotic thrombocytopenic purpura
P2860
Q21202864-645F35CF-08CD-4B43-B0CB-C4FDF81D32D3Q24315130-541B979A-25C5-42E6-9E34-15F57E405CE6Q24658043-64144DA9-B1CD-44EA-B2B4-72E81922A990Q24676319-C0576BEE-CDE0-4508-B48D-8210737F846DQ33330770-91ED4955-D5C5-492F-85CF-1F66EF9DF81DQ33335833-401BB4C3-D3B1-44A2-9D53-203D833858F6Q33335836-1B272244-F8A0-42CF-84AD-1D2E608318F1Q33344694-15639870-167C-4391-B489-B009A55B6541Q33345226-EB62A705-9AB9-4F5B-8035-ACB2955E2CC3Q33345537-D549CE2E-523E-4C81-9EAB-D10285B26D1AQ33349831-D4059D53-7D35-4780-8BB6-C6DF429D95ECQ33358128-3FC24147-C00B-4ACF-AC5C-591C31A3B0A2Q33364421-0DA6CD9A-BAF3-4B27-AA91-85846D61C09AQ33368691-2A3CBC72-46A1-403D-9049-1EAAC30957F6Q33369891-F6604171-D87D-4A5B-A284-413BDE701AD6Q33375833-08A6079F-E479-43BE-B4E6-9BBCBB72E683Q33377799-055F615D-2F8C-4C7A-82ED-F9A3FC5D4EE1Q33378236-E5D11F2C-4A4D-42CB-AF9C-3EE3BB0E5202Q33385215-9830E7DF-2682-4E06-A1D7-769FB5B53299Q33390198-A423270B-2C90-49FB-BCB5-6AC7DF6D91BEQ33390761-6096862A-1226-4F34-B65C-05D1410FA72EQ34067107-94722FEB-9329-48FE-89B3-2ACDEE986BCBQ35639388-FA403275-D5F1-4D9D-AF5A-17D6C765F726Q35748229-D15E2D1A-CB7D-40E1-84EB-2134DD6780E5Q36057084-CF5B392E-1097-449A-ACD2-7DD4F2CBE02EQ36405585-4D312F3E-E279-4800-AA44-BCD8B938968CQ36506391-D7E4169A-54E5-417E-8296-742B95198A09Q37106302-96E5B57E-3A89-4818-9B0A-1990621C781DQ37181643-F835B9D9-0279-4622-B95D-30B70C792058Q40262931-25E99A3F-B877-4297-8A31-8DB449A1E5EBQ40960179-B2408381-DEE6-4FEC-B97C-E687CAE22F88Q48275599-05A116FA-BEC1-4205-A8BE-11543DAC763FQ48338971-E99283D7-0291-40DE-A381-A16F4A7CEF9BQ57591162-303E45F1-4533-4A03-8F4B-0FAB11697CE2
P2860
Familial hemolytic-uremic syndrome and homozygous factor H deficiency.
description
1994 nî lūn-bûn
@nan
1994 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Familial hemolytic-uremic syndrome and homozygous factor H deficiency.
@ast
Familial hemolytic-uremic syndrome and homozygous factor H deficiency.
@en
type
label
Familial hemolytic-uremic syndrome and homozygous factor H deficiency.
@ast
Familial hemolytic-uremic syndrome and homozygous factor H deficiency.
@en
prefLabel
Familial hemolytic-uremic syndrome and homozygous factor H deficiency.
@ast
Familial hemolytic-uremic syndrome and homozygous factor H deficiency.
@en
P2093
P1476
Familial hemolytic-uremic syndrome and homozygous factor H deficiency.
@en
P2093
P304
P356
10.1016/S0272-6386(12)81065-1
P577
1994-12-01T00:00:00Z