Evaluation of Hemopoietic Disorders and Renal Function in Children with Chronic Glomerulonephritis Depending on Allelic Gene Polymorphism of IL-10 and IL-1β

We have examined 20 children suffering from chronic glomerulonephritis with torpid course of disease and persistent urinary syndrome. It was defined that in children with torpid course of disease genotype C/T gene IL-1β (-511) (p < 0.05) was significantly more common. Also, we found the relations...

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Auteurs principaux: V.M. Dudnyk (Auteur), G.Yu. Zvenigorodska (Auteur)
Format: Livre
Publié: Zaslavsky O.Yu., 2012-03-01T00:00:00Z.
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