نتایج جستجو برای: primary immunodeficiency disease

تعداد نتایج: 2088150  

2015
Morvarid Oveisi Oriyah Barzilay Ahmed A. Hanafi

Primary immunodeficiency diseases are rare hereditary conditions that usually occur at a young age; however, secondary immunodeficiency is acquired due to disease, drug treatment and is increasing in frequency among the population. Although periodontal diseases related to these conditions are secondary to other life threatening manifestations, they are very common and easily detectable by the p...

2012
Umezurike Hughes Okafor

The following conditions and diseases that are associated with primary immunodeficiency disorder include, Combined variable immunodeficiency disease, Ataxia-telangiectasia, Chediak-Higashi syndrome, Complement deficiencies, DiGeorge syndrome, Hypogammaglobulinemia, Job syndrome, Leukocyte adhesion defects, Bruton disease, Congenital agammaglobulinemia, Selective deficiency of IgA, Wiscott-Aldri...

Journal: :iranian journal of allergy, asthma and immunology 0
toshio miyawaki

epstein-barr virus (ebv) is a ubiquitous human -herpesvirus that infects about 95% of the adult population. the majority of primary infections occurs in early childhood and is generally subclinical; it can cause infectious mononucleosis (im), which is usually a self-limiting lymphoproliferative disorder. however, infection of ebv occasionally results in severe, often lethal diseases, which inc...

Journal: :iranian journal of allergy, asthma and immunology 0
m. movahedi a. aghamohammadi a. farhondi m. moin zahra pourpak m. gharagozlou

chronic granulomatous disease represents a group of inherited disorders of phagocytic system wherein recurrent infections are seen at different sites especially in the respiratory system. to determine the clinical spectrum of respiratory manifestations in chronic granulomatous disease patients, in this retrospective study, we used data from iranian primary immunodeficiency registry. the diagnos...

Journal: :Haematologica 2013
Gertjan J Driessen Virgil A S H Dalm P Martin van Hagen H Anne Grashoff Nico G Hartwig Annemarie M C van Rossum Adilia Warris Esther de Vries Barbara H Barendregt Ingrid Pico Sandra Posthumus Menno C van Zelm Jacques J M van Dongen Mirjam van der Burg

Patients with hypogammaglobulinemia who do not fulfill all the classical diagnostic criteria for common variable immunodeficiency (reduction of two immunoglobulin isotypes and a reduced response to vaccination) constitute a diagnostic and therapeutic dilemma, because information concerning the clinical and immunological characteristics of these patients with idiopathic primary hypogammaglobulin...

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