Items where Author is "Kotlarz, D."

Article

(2021) Congenital disorders of glycosylation with defective fucosylation. JOURNAL OF INHERITED METABOLIC DISEASE. pp. 1441-1452. ISSN 0141-8955 1573-2665 J9 - J INHERIT METAB DIS

(2020) NOX1 Regulates Collective and Planktonic Cell Migration: Insights From Patients With Pediatric-Onset IBD and NOX1 Deficiency. Inflammatory Bowel Diseases. pp. 1166-1176. ISSN 1078-0998

(2019) Enigmas of IL-12R1 Deficiency: Contemporary of Two Disease, Mendelian Susceptibility to Mycobacterial Disease and Crohn Disease. Journal of Clinical Immunology. S66-S67. ISSN 0271-9142

(2019) IL-12Rbeta1 deficiency corresponding to concurrency of two diseases, mendelian susceptibility to mycobacterial disease and Crohn's disease. J Clin Tuberc Other Mycobact Dis. p. 100123. ISSN 2405-5794 (Electronic) 2405-5794 (Linking)

(2019) An analysis and survey of interleukin-10 receptor mutation in inflammatory bowel disease (IBD) in the first Iranian IBD cohort. Journal of Laboratory Medicine. pp. 185-189. ISSN 2567-9430

(2018) Impaired IL-12-and IL-23-Mediated Immunity Due to IL-12R1 Deficiency in Iranian Patients with Mendelian Susceptibility to Mycobacterial Disease. Journal of Clinical Immunology. pp. 787-793. ISSN 0271-9142

(2017) Myb-like, SWIRM, and MPN domains 1 (MYSM1) deficiency: Genotoxic stress-associated bone marrow failure and developmental aberrations. Journal of Allergy and Clinical Immunology. pp. 1112-1119. ISSN 0091-6749