@Article{Polańska2009,
journal="Central European Journal of\ Immunology",
issn="1426-3912",
volume="34",
number="3",
year="2009",
title="Review paper Chronic granulomatous disease \– primary phagocytic immunodeficiency",
abstract="Chronic granulomatous disease (CGD) is a rare hereditary primary immunodeficiency, in which defective production of microbicidal oxidants by phagocytes (neutrophils, eosinophils, monocytes, and macrophages) leads to severe recurrent infections. This article reviews pathogenesis, diagnostic criteria, clinical signs, and treatment of CGD.",
author="Polańska, Bożena",
pages="182--191",
url="https://www.termedia.pl/Review-paper-Chronic-granulomatous-disease-8211-primary-phagocytic-immunodeficiency,10,13193,1,1.html"
}