Items where Author is "Klein, C."

Article

(2021) Genetic Analysis of a Cohort of 275 Patients with Hyper-IgE Syndromes and/or Chronic Mucocutaneous Candidiasis. JOURNAL OF CLINICAL IMMUNOLOGY. pp. 1804-1838. ISSN 0271-9142 1573-2592 J9 - J CLIN IMMUNOL

(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

(2020) A case report of sinusoidal diffuse large B-cell lymphoma in a STK4 deficient patient. Medicine. ISSN 0025-7974

(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) Proteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent Acquisition. Molecular & Cellular Proteomics. pp. 760-772. ISSN 1535-9476

(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

(2018) Pregnancy, child bearing and prevention of giving birth to the affected children in patients with primary immunodeficiency disease; a case-series. Bmc Pregnancy and Childbirth. ISSN 1471-2393

(2017) EBV lymphoproliferative-associated disease and primary cardiac T-cell lymphoma in a STK4 deficient patient. Medicine (United States). ISSN 00257974 (ISSN)

(2017) EBV lymphoproliferative-associated disease and primary cardiac T-cell lymphoma in a STK4 deficient patient A case report. Medicine. ISSN 0025-7974

(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