(Q51333222)

3 April 2018

title

Antibody mediated rejection associated with complement factor h-related protein 3/1 deficiency successfully treated with eculizumab. (English)

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3

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Guido Filler

9

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author name string

D Noone

1

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J Al-Matrafi

2

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P F Zipfel

4

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A M Herzenberg

5

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P S Thorner

6

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F G Pluthero

7

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W H A Kahr

8

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D Hebert

10

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E Harvey

11

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C Licht

12

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language of work or name

English

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publication date

8 June 2012

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American Journal of Transplantation

published in

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volume

12

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issue

9

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page(s)

2546-2553

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Antibody-mediated rejection in kidney transplantation: an update

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

Antibody-mediated rejection criteria - an addition to the Banff 97 classification of renal allograft rejection

21 January 2018

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Thrombotic thrombocytopenia purpura (TTP) and other thrombotic microangiopathies

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Thrombotic microangiopathy and peritubular capillary C4d expression in renal allograft biopsies

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https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

Treatment options and strategies for antibody mediated rejection after renal transplantation

21 January 2018

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Inhibiting the C5-C5a receptor axis

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

Treatment of paroxysmal nocturnal hemoglobinuria in the era of eculizumab

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

Complement inhibitor eculizumab in atypical hemolytic uremic syndrome

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

The use of antibody to complement protein C5 for salvage treatment of severe antibody-mediated rejection

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

Rejection of the kidney allograft

21 January 2018

1 reference

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Thrombotic microangiopathy after kidney transplantation

21 January 2018

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Eculizumab for the treatment of de novo thrombotic microangiopathy post simultaneous pancreas-kidney transplantation--a case report

21 January 2018

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Complement inhibition enables renal allograft accommodation and long-term engraftment in presensitized nonhuman primates

21 January 2018

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The human complement factor H: functional roles, genetic variations and disease associations

21 January 2018

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An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD)

21 January 2018

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Metabolism of the fifth component of complement, and its relation to metabolism of the third component, in patients with complement activation

21 January 2018

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Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

21 January 2018

1 reference

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Mutations of factor H impair regulation of surface-bound C3b by three mechanisms in atypical hemolytic uremic syndrome

21 January 2018

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Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation

21 January 2018

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DEAP-HUS: deficiency of CFHR plasma proteins and autoantibody-positive form of hemolytic uremic syndrome

21 January 2018

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Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

Genome-wide association study identifies susceptibility loci for IgA nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

Complement Mutation-AssociatedDe NovoThrombotic Microangiopathy Following Kidney Transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-6143.2012.04124.X

10.1111/J.1600-6143.2012.04124.X

21 January 2018

Identifiers

DOI

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3 April 2018

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3 April 2018