Novel factor H mutation associated with familial membranoproliferative glomerulonephritis type I.

about

Anti-Factor B and Anti-C3b Autoantibodies in C3 Glomerulopathy and Ig-Associated Membranoproliferative GN.Diseases of complement dysregulation-an overview.

P2860

Q39016179-900B86A6-EEAA-43E0-AAC3-9B2756B5961C Q48256943-05466676-F094-45E1-ACA4-A6F1C70EC398

P2860

Novel factor H mutation associated with familial membranoproliferative glomerulonephritis type I.

Item

http://www.wikidata.org/entity/Q40626473

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Novel factor H mutation associ ...... ive glomerulonephritis type I.

@en

type

Item

label

Novel factor H mutation associ ...... ive glomerulonephritis type I.

@en

prefLabel

Novel factor H mutation associ ...... ive glomerulonephritis type I.

@en

P1476

Novel factor H mutation associ ...... tive glomerulonephritis type I

@en

P2093

Miriam Davidovits

http://www.w3.org/2001/XMLSchema#string

P2860

Membranoproliferative glomerulonephritis--a new look at an old entity

Eculizumab in a patient with dense-deposit disease

Eculizumab for the Treatment of Dense-Deposit Disease

Eculizumab and Refractory Membranoproliferative Glomerulonephritis

Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.

Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome.

Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.

Dense deposit disease: clinicopathologic study of 32 pediatric and adult patients

Atypical hemolytic-uremic syndrome.

Efficacy of eculizumab in a patient with factor-H-associated atypical hemolytic uremic syndrome.

P2888

s00467-015-3166-7

P304

2129-2134

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1007/S00467-015-3166-7

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Hadas Alfandary

P577

2015-08-20T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P6179

1039740689

http://www.w3.org/2001/XMLSchema#string

P698

26289290

http://www.w3.org/2001/XMLSchema#string

P921

glomerulonephritis

Novel factor H mutation associated with familial membranoproliferative glomerulonephritis type I.

about

P2860

P2860

Novel factor H mutation associated with familial membranoproliferative glomerulonephritis type I.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P921

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P921