Complement related kidney diseases: Recurrence after transplantation. - Wikidata - wikimedia - TriplyDB

Complement related kidney diseases: Recurrence after transplantation.

Complement related kidney diseases: Recurrence after transplantation.

http://www.wikidata.org/entity/Q37522557

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Ficolin-2 Gene rs7851696 Polymorphism is Associated with Delayed Graft Function and Acute Rejection in Kidney Allograft Recipients.Mesenchymal Stem Cells Control Complement C5 Activation by Factor H in Lupus Nephritis.Complement-mediated renal diseases after kidney transplantation - current diagnostic and therapeutic options in and recurrent diseases Thrombotic microangiopathy after renal transplantation: Current insights in and recurrent disease

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P2860

Complement related kidney diseases: Recurrence after transplantation.

http://www.wikidata.org/entity/Q37522557

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on December 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Complement related kidney diseases: Recurrence after transplantation.

@en

Complement related kidney diseases: Recurrence after transplantation.

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type

label

Complement related kidney diseases: Recurrence after transplantation.

@en

Complement related kidney diseases: Recurrence after transplantation.

@nl

prefLabel

Complement related kidney diseases: Recurrence after transplantation.

@en

Complement related kidney diseases: Recurrence after transplantation.

@nl

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P1433

World journal of transplantation

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Complement related kidney diseases: Recurrence after transplantation.

@en

P2093

Elisabetta Bertoni

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Maurizio Salvadori

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P2860

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

Recurrent atypical hemolytic uremic syndrome associated with factor I mutation in a living related renal transplant recipient

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

Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis

Pre-emptive eculizumab and plasmapheresis for renal transplant in atypical hemolytic uremic syndrome

Eculizumab for dense deposit disease and C3 glomerulonephritis

Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome

Disease recurrence in paediatric renal transplantation

Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

Reclassification of membranoproliferative glomerulonephritis: Identification of a new GN: C3GN

P304

632-645

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scholarly article

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10.5500/WJT.V6.I4.632

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4

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6

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2016-12-01T00:00:00Z

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28058212

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5175220

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