Acquired partial lipodystrophy and C3 glomerulopathy: Dysregulation of the complement system as a common mechanism-Reference-Cited by-同舟云学术

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Acquired partial lipodystrophy and C3 glomerulopathy: Dysregulation of the complement system as a common mechanism

Published:2018-05 Issue:3 Volume:38 Page:258-266
ISSN:2013-2514
Container-title:Nefrología (English Edition)
language:en
Short-container-title:Nefrología (English Edition)

Author:

Corvillo Fernando,López-Trascasa Margarita

Funder

Instituto de Salud Carlos III Health Research Fund

Sociedad Española de Nefrología (Spanish Society of Nephrology) (Fundación SENEFRO Aid for Research, 2016)

CIBERER (Center for Biomedical Network Research on Rare Diseases)

Publisher

Elsevier BV

Subject

Nephrology

Reference32 articles.

1. Complement: a key system for immune surveillance and homeostasis;Ricklin;Nat. Immunol.,2010

2. Properdin: a tightly regulated critical inflammatory modulator;Blatt;Immunol. Rev.,2016

3. The complotype: dictating risk for inflammation and infection;Harris;Trends Immunol.,2012

4. All things complement;Thurman;Clin J Am Soc Nephrol,2016

5. Autoantibodies to complement components in C3 glomerulopathy and atypical hemolytic uremic syndrome;Józsi;Immunol. Lett.,2014

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Barraquer-Simons Syndrome: An Unusual Form of Acquired Partial Lipodystrophy in a Child with Lupus Nephritis;Indian Dermatology Online Journal;2023

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