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(2024) Early diagnosis of immunodeficient patients with partial albinism: The role of hair study and peripheral blood smear. Pediatric Allergy and Immunology. ISSN 09056157 (ISSN)
(2021) The critical role of prenatal genetic study in prevention of primary immunodeficiency in high-risk families: The largest report of 107 cases. Iranian Journal of Allergy, Asthma and Immunology. pp. 478-483.
(2020) Recent developments in electrochemical sensors for detecting hydrazine with different modified electrodes. RSC Advances. pp. 30481-30498.
(2019) Comparison of interleukin 17 and interleukin 22 inflammatory cytokines in peripheral blood mononuclear cells of children with and without asthma. Journal of Isfahan Medical School. pp. 1376-1381. ISSN 10277595 (ISSN)
(2012) MOLECULAR ANALYSIS OF CHRONIC GRANULOMATOUS DISEASE CAUSED BY DEFECTS IN NCF-2: THE GENE ENCODING THE P67-<i>PHOX</i>. Journal of clinical immunology. p. 229. ISSN 0271-9142
(2012) Molecular Analysis of Four Cases of Chronic Granulomatous Disease Caused by Defects in NCF-2: The Gene Encoding the p67-<i>phox</i>. Iranian Journal of Allergy Asthma and Immunology. pp. 340-344. ISSN 1735-1502
(2012) Molecular analysis of four cases of chronic granulomatous disease caused by defects in NCF-2: The gene encoding the p67-phox. Iranian Journal of Allergy, Asthma and Immunology. pp. 340-344. ISSN 17355249 (ISSN)
(2011) Inheritance Pattern and Clinical Aspects of 93 Iranian Patients with Chronic Granulomatous Disease. Journal of clinical immunology. pp. 792-801. ISSN 0271-9142
(2010) Inheritance pattern and clinical aspects of chronic granulomatous disease in Iran. Allergy. p. 114. ISSN 0105-4538