Liver transplantation for aHUS: still needed in the eculizumab era? - Wikidata - wikimedia - TriplyDB

Liver transplantation for aHUS: still needed in the eculizumab era?

Liver transplantation for aHUS: still needed in the eculizumab era?

http://www.wikidata.org/entity/Q33427846

about

Reclassification of membranoproliferative glomerulonephritis: Identification of a new GN: C3GN At the Cross Section of Thrombotic Microangiopathy and Atypical Hemolytic Uremic Syndrome: A Narrative Review of Differential Diagnostics and a Problematization of Nomenclature.Outcomes of patients with atypical haemolytic uraemic syndrome with native and transplanted kidneys treated with eculizumab: a pooled post hoc analysis.Kidney Transplantation in Patients with Atypical Hemolytic Uremic Syndrome due to Complement Factor H Deficiency: Impact of Liver Transplantation.Long-term outcomes of the Atypical Hemolytic Uremic Syndrome after kidney transplantation treated with eculizumab as first choice.Combined and sequential liver-kidney transplantation in children.Long-term successful liver-kidney transplantation in a child with atypical hemolytic uremic syndrome caused by homozygous factor H deficiency.Thrombotic microangiopathy after renal transplantation: Current insights in and recurrent disease

P2860

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P2860

Liver transplantation for aHUS: still needed in the eculizumab era?

http://www.wikidata.org/entity/Q33427846

description

2015 nî lūn-bûn

@nan

2015 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

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

name

Liver transplantation for aHUS: still needed in the eculizumab era?

@ast

Liver transplantation for aHUS: still needed in the eculizumab era?

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type

label

Liver transplantation for aHUS: still needed in the eculizumab era?

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Liver transplantation for aHUS: still needed in the eculizumab era?

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prefLabel

Liver transplantation for aHUS: still needed in the eculizumab era?

@ast

Liver transplantation for aHUS: still needed in the eculizumab era?

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S00467-015-3278-0

P1433

Pediatric Nephrology

P1476

Liver transplantation for aHUS: still needed in the eculizumab era?

@en

P2093

Alessandro Amore

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

Andrea Brunati

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Eliana Gotti

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Erica Daina

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Marina Noris

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Mauro Salizzoni

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Miriam Galbusera

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R Licia Peruzzi

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Renato Romagnoli

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Roberto Bonaudo

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P2860

Characterization of mutations in severe methylenetetrahydrofolate reductase deficiency reveals an FAD-responsive mutation

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype

Structural and functional characterization of the product of disease-related factor H gene conversion

Complement factor H and related proteins: an expanding family of complement-regulatory proteins?

Improved survival with plasma exchange in patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome.

Combined kidney and liver transplantation for familial haemolytic uraemic syndrome.

von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome.

Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.

Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32.

P2888

s00467-015-3278-0

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759-768

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5

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31

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Giuseppe Remuzzi

P577

2015-11-24T00:00:00Z

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284711860

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P921

liver transplantation