Evaluation of complement regulatory components in patients with atypical hemolytic uremic syndrome

BACKGROUND: Atypical hemolytic uremic syndrome (aHUS), a rare disorder characterized by thrombocytopenia, microangiopathic hemolytic anemia, and acute renal failure, is associated with mutations and polymorphisms in various components and regulators of the complement alternative pathway (AP), includ...

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Detalles Bibliográficos
Autores principales: Soudabeh, Hosseini, Ebrahim, Kalantar, Nakisa, Hooman, Akbar, Dorgalaleh, Rozita, Hosseini Shamsabadi, Bamedi, Taregh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Society of Experimental and Clinical Immunology 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439977/
https://www.ncbi.nlm.nih.gov/pubmed/26155102
http://dx.doi.org/10.5114/ceji.2014.42127

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439977/
https://www.ncbi.nlm.nih.gov/pubmed/26155102
http://dx.doi.org/10.5114/ceji.2014.42127

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