Items where Author is "Sherkat, R."

Article

(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) 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) 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

(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