Items where Author is "Sherkat, R."

(2022) Ciliary and immune dysfunctions and their genetic background in patients with non-cystic fibrosis bronchiectasis in Central Iran. Ir J Med Sci. ISSN 0021-1265

(2022) Clinical and Laboratory Parameters of Autoinflammatory Disorders in Single Tertiary Care Center. IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY. pp. 197-206. ISSN 1735-1502 1735-5249 J9 - IRAN J ALLERGY ASTHM

(2022) Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and Gains. J Clin Immunol. pp. 1083-1092. ISSN 0271-9142 (Print) 0271-9142

(2022) The First Iranian Cohort of Pediatric Patients with Activated Phosphoinositide 3-Kinase-δ (PI3Kδ) Syndrome (APDS). Immunological Investigations. pp. 644-659. ISSN 08820139 (ISSN)

(2022) Spontaneous regression of diffuse large B-cell lymphoma in a patient with ataxia-telangiectasia. ADVANCED BIOMEDICAL RESEARCH. ISSN 2277-9175 J9 - ADV BIOMED RES-INDIA

(2021) Autoimmune manifestations among 461 patients with monogenic inborn errors of immunity. Pediatr Allergy Immunol. pp. 1335-1348. ISSN 0905-6157

(2021) Component-Resolved Diagnosis of American Cockroach (Periplaneta americana) Allergy in Patients From Different Geographical Areas. Front Allergy. p. 691627. ISSN 2673-6101 (Print) 2673-6101

(2021) Dimethylaminoparthenolide (DMAPT) as an alternative approach for treatment of Familial Mediterranean Fever (FMF). IRANIAN JOURNAL OF BASIC MEDICAL SCIENCES. pp. 1421-1427. ISSN 2008-3866 2008-3874 J9 - IRAN J BASIC MED SCI

(2021) Diversity of HLA class I and class II alleles in Iran populations: Systematic review and Meta-Analaysis. TRANSPLANT IMMUNOLOGY. ISSN 0966-3274 1878-5492 J9 - TRANSPL IMMUNOL

(2021) Functional analysis of two STAT1 gain-of-function mutations in two Iranian families with autosomal dominant chronic mucocutaneous candidiasis. Medical Mycology. pp. 180-188. ISSN 1369-3786

(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

(2021) Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update). BLOOD CELLS MOLECULES AND DISEASES. ISSN 1079-9796 1096-0961 J9 - BLOOD CELL MOL DIS

(2021) Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy. Cell. 3812-+. ISSN 0092-8674

(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

(2016) Evaluation of mutation in B cell maturation antigen (BCMA) gene in patients with common variable immunodeficiency (CVID). Journal of Isfahan Medical School. pp. 555-562. ISSN 10277595 (ISSN)

(2016) Gene mutations responsible for primary immunodeficiency disorders: A report from the first primary immunodeficiency biobank in Iran. Allergy Asthma and Clinical Immunology. ISSN 1710-1484

(2016) Investigating the frequency of the peripheral blood B and transitional B cells in the patients with common variable immunodeficiency. Journal of Isfahan Medical School. pp. 1851-1856. ISSN 10277595 (ISSN)

(2015) Primary Antibody Deficiency in a Tertiary Referral Hospital: A 30-Year Experiment. Journal of Investigational Allergology and Clinical Immunology. pp. 416-425. ISSN 1018-9068