Items where Author is "Sherkat, R."

Article

(2026) The Coexistence of Asthma and Common Variable Immunodeficiency in a Patient with TNFRSF13B Gene Mutation. Iranian Journal of Allergy Asthma and Immunology. pp. 264-268. ISSN 1735-1502

(2026) Genotype-phenotype correlations and cancer risk in monogenic epidermodysplasia verruciformis. Journal of the European Academy of Dermatology and Venereology : JEADV. e755-e758. ISSN 1468-3083 (Electronic) 0926-9959 (Print) 0926-9959 (Linking)

(2026) Human LFA-1 governs T cell immune surveillance of the skin. Science Immunology. p. 30. ISSN 2470-9468

(2026) Low-Dose Prednisolone Therapy before Pregnancy Positively Impacts the Increase of Granulocytic Myeloid-Derived Suppressor Cells Relative Monocytic MDSCs, Compared to Lymphocyte Immunotherapy, in Women with Recurrent Miscarriages. Iranian journal of immunology : IJI. p. 3. ISSN 1735-367X (Electronic) 1735-1383 (Linking)

(2025) Association Between Pathogenic Variants in NLRP12 and Autoinflammatory Disease: A Comprehensive Systematic Review. International Journal of Immunogenetics. pp. 233-248. ISSN 1744-3121

(2025) Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registry. Frontiers in Genetics. p. 17.

(2025) Clinicogenetic characterisation of SLC29A3-related syndromes: a case series, tracing ancestral variants and molecular dynamics simulation. Journal of Medical Genetics. p. 12. ISSN 0022-2593

(2025) DOCK2 Deficiency and GATA2 Haploinsufficiency Can Underlie Critical Coronavirus Disease 2019 (COVID-19) Pneumonia. Journal of Clinical Immunology. p. 14. ISSN 0271-9142

(2025) Decreased expression of hsa-miR-142-3p and hsa-miR-155-5p in common variable immunodeficiency and involvement of their target genes and biological pathways. Allergologia Et Immunopathologia. pp. 153-169. ISSN 0301-0546

(2025) Evaluation of the Sixth Exon of IL12RB1 in Patients Afflicted by the Non-Healing Form of Cutaneous Leishmaniasis. Current Genetic Medicine Reports. p. 7.

(2025) Exploring Monogenic, Polygenic, and Epigenetic Models of Common Variable Immunodeficiency. Human Mutation. ISSN 10597794 (ISSN)

(2025) Extended clinical phenotypes and treatment modalities in 32 JAGN1-deficient patients: a multicenter study by ESID and EBMT IEWP. Blood Advances. pp. 1702-1711. ISSN 2473-9529

(2025) Guillain-Barré syndrome (GBS) after severe/critical COVID-19 or COVID-19 vaccination. European Journal of Medical Research. p. 7. ISSN 0949-2321

(2025) Guillain-Barré syndrome (GBS) after severe/critical COVID-19 or COVID-19 vaccination. European Journal of Medical Research. p. 7. ISSN 0949-2321

(2025) A Systematic Review of Mendelian Pyoderma Gangrenosum: Clinical and Genetic Characteristics in 120 Published Patients. Experimental Dermatology. p. 16. ISSN 0906-6705

(2025) Unraveling a novel missense mutation (c.A248C) in Wiskott-Aldrich syndrome gene by whole exome sequencing: Insights from dynamic simulation, molecular docking and in-silico studies. International Immunopharmacology. p. 11. ISSN 1567-5769

(2025) A novel ITGB2 variant in a patient with severe recurrent pyoderma gangrenosum-like lesions and underlying leukocyte adhesion deficiency type I: case report and literature review. Archives of Dermatological Research. p. 9. ISSN 0340-3696

(2024) B-cells absence in patients diagnosed as inborn errors of immunity: a registry-based study. Immunogenetics. pp. 189-202. ISSN 0093-7711

(2024) Clinical heterogeneity in families with multiple cases of inborn errors of immunity. Clinical Immunology. p. 11. ISSN 1521-6616

(2024) Diversity in the Clinical Course and Outcome of COVID-19 in Patients with Different Inborn Errors of Immunity can be Associated with the Type of Error. Advanced Biomedical Research. p. 11. ISSN 2277-9175

(2024) Hyper IgE Cases with novel genotypes and phenotypes: How Different Do They Present? Clinical Immunology. p. 1. ISSN 1521-6616

(2024) Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review. Genetics in Medicine. p. 33. ISSN 1098-3600

(2024) Noninfectious Complications in B-Lymphopenic Common Variable Immunodeficiency. Journal of Investigational Allergology and Clinical Immunology. pp. 233-245. ISSN 1018-9068

(2024) The sufficiency of genetic diagnosis in managing patients with inborn errors of immunity during prenatal care and childbearing. Immunogenetics. pp. 271-277. ISSN 0093-7711

(2023) Ciliary and immune dysfunctions and their genetic background in patients with non-cystic fibrosis bronchiectasis in Central Iran. Irish journal of medical science. pp. 277-283. ISSN 1863-4362 (Electronic) 0021-1265 (Linking)

(2023) Clinical and immunological characteristics of 69 leukocyte adhesion deficiency-I patients. Pediatric Allergy and Immunology. p. 12. ISSN 0905-6157

(2023) Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG <i>RFXANK</i> Founder Mutation in the Iranian Population. Journal of Clinical Immunology. pp. 1941-1952. ISSN 0271-9142

(2023) Contradictory Effect of Lymphocyte Therapy and Prednisolone Therapy on CD3<SUP>+</SUP>CD8<SUP>+</SUP>CD56<SUP>+</SUP> Natural Killer T Population in Women with Recurrent Spontaneous Abortion. Journal of Human Reproductive Sciences. pp. 246-256. ISSN 0974-1208

(2023) Cytomegalovirus specific cell-mediated immunity status in women with preeclampsia: A case-control study. Advanced Biomedical Research. p. 5. ISSN 2277-9175

(2023) Hematologically important mutations: Leukocyte adhesion deficiency (second update). Blood Cells Molecules and Diseases. p. 14. ISSN 1079-9796

(2023) Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency. The Journal of experimental medicine. ISSN 1540-9538 (Electronic) 0022-1007 (Print) 0022-1007 (Linking)

(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) Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and Gains. Journal of Clinical Immunology. pp. 1083-1092. ISSN 0271-9142

(2022) Developing a logo therapy focused program for individual with common variable immunodeficiency disease (CVID): Efficacy on resilience and quality of life. Clinical and Experimental Allergy. p. 1018. ISSN 0954-7894

(2022) Diversity of malignancies in patients with different types of inborn errors of immunity. Allergy Asthma and Clinical Immunology. p. 9. ISSN 1710-1492

(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) Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency. Journal of Experimental Medicine. p. 31. ISSN 0022-1007

(2022) Impaired IL-23-dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency. Journal of Experimental Medicine. p. 33. ISSN 0022-1007

(2022) Spontaneous Regression of Diffuse Large B-cell Lymphoma in a Patient with Ataxia-Telangiectasia. Advanced Biomedical Research. p. 31. ISSN 2277-9175 (Print) 2277-9175 (Electronic) 2277-9175 (Linking)

(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) 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

(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