Bilimsel çalışmalar
Prof. Dr. Çiğdem Aydoğmuş
102 yayın. Her yayının yanında bilginin kaynağı yazar.
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Clinical Manifestations and Immunologic Phenotype in Patients With RAG1/2 Mutations: A Single Centre Experience and Description of A Novel Mutation
Scandinavian Journal of Immunology, 2026
DOI 10.1111/sji.70116 PMID 42032428 Kaynak: OpenAlex
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Recent Thymic Emigrant Levels in Inborn Errors of Immunity: Is Their Diagnostic Value Greater Than We Think?
Scandinavian Journal of Immunology, 2026
DOI 10.1111/sji.70133 PMID 42385203 Kaynak: OpenAlex
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Clinical Spectrum of Cutaneous, Ocular, and Hair Manifestations in Patients With Inborn Errors of Immunity: Insights From a Single Center in Turkey
Immunity Inflammation and Disease, 2026
DOI 10.1002/iid3.70384 PMID 41738375 Açık erişimli tam metinKaynak: OpenAlex
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Pediatric Severe Cutaneous Adverse Drug Reactions: Clinical Characteristics and Comparison of Causality Assessment Tools and Severity Scoring Systems in Relation to Clinical Outcomes from a Single-Center Experience
International Archives of Allergy and Immunology, 2026
DOI 10.1159/000551609 PMID 41955167 Kaynak: OpenAlex
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From Idiopathic to Identifiable: Oral Mite Sensitization Revealed by Component-Resolved Diagnostics
Pediatric Allergy Immunology and Pulmonology, 2026
DOI 10.1177/2151321x261448302 PMID 42085204 Kaynak: OpenAlex
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Successful Rapid Desensitization with Nitrofurantoin in a Patient with Multiple Drug Allergy Syndrome
Pediatric Allergy Immunology and Pulmonology, 2026
DOI 10.1177/2151321x261459959 PMID 42267790 Kaynak: OpenAlex
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A Rare Pediatric Case of Valproic Acid-Induced Dress Syndrome with Concomitant Pulmonary and Hepatic Involvement
Pediatric Allergy Immunology and Pulmonology, 2026
DOI 10.1177/2151321x261486686 PMID 42713870 Kaynak: OpenAlex
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Disseminated Tuberculosis and Early-Onset SLE in a Child with a Novel STAT1 Gain-of-Function Mutation: a Case Report
Journal of Clinical Immunology, 2026
DOI 10.1007/s10875-026-02040-y PMID 42319627 Açık erişimli tam metinKaynak: ORCID
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When cure is not enough: Parental anxiety, depression, and caregiver burden after HSCT for inborn errors of immunity
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 2026
DOI 10.1111/pai.70543 PMID 42969273 Kaynak: Europe PMC
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Beyond immune recovery: Quality of life and psychosocial challenges in children with inborn errors of immunity after transplantation
Irish journal of medical science, 2026
DOI 10.1007/s11845-026-04480-2 PMID 42287508 Açık erişimli tam metinKaynak: Europe PMC
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Immune Checkpoint Dysfunction Remodels Adaptive Immune Receptor Repertoires in CTLA-4 Insufficiency and LRBA Deficiency
Clinical reviews in allergy & immunology, 2026
DOI 10.1007/s12016-026-09209-8 PMID 42895678 Kaynak: Europe PMC
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A Novel Phosphoglucomutase-3 Gene Variant Causing Milder Phenotype in Two Families
Journal of Clinical Immunology, 2026
DOI 10.1007/s10875-026-02012-2 PMID 41904308 Açık erişimli tam metinKaynak: OpenAlex
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Selective IgA deficiency and allergic diseases: Clinical and immunological evaluation
Allergologia et Immunopathologia, 2025
DOI 10.15586/aei.v53i5.1374 PMID 40923423 1 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Enhancing Primary Immunodeficiency Diagnosis: Findings From Targeted Genetic Testing in a Turkish Cohort
Scandinavian Journal of Immunology, 2025
DOI 10.1111/sji.70031 PMID 40518733 Açık erişimli tam metinKaynak: OpenAlex
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Early-onset neutropenia and mixed phenotype in ADA2 deficiency: diagnostic and therapeutic challenges
Frontiers in Immunology, 2025
DOI 10.3389/fimmu.2025.1639318 PMID 41112235 Açık erişimli tam metinKaynak: OpenAlex
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Monocyte plasticity and HLA-DR expression in patients with X-linked agammaglobulinemia
Immunologic Research, 2025
DOI 10.1007/s12026-025-09690-x PMID 40970998 Kaynak: OpenAlex
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Expansion of Myeloid‐Derived Suppressor Cells and Lymphocyte Apoptosis Beyond B‐Cell Deficiency in X‐Linked Agammaglobulinemia
Scandinavian Journal of Immunology, 2025
DOI 10.1111/sji.70063 PMID 41208023 Açık erişimli tam metinKaynak: OpenAlex
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Evaluation of T-cell repertoire by flow cytometric analysis in primary immunodeficiencies with DNA repair defects
Scandinavian journal of immunology, 2025
DOI 10.1111/sji.70003 PMID 39967281 3 atıf (Europe PMC) Açık erişimli tam metinKaynak: Europe PMC
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Abatacept restores dysregulated transcriptomic and proteomic profile in disorders of CTLA-4 insufficiency
Journal of Allergy and Clinical Immunology, 2025
DOI 10.1016/j.jaci.2025.08.027 PMID 40967277 9 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Comprehensive αβ T‐Cell Receptor Repertoire Analysis Reveals a Unique CD8+ TCR Landscape in DOCK8‐Deficient Patients
Allergy, 2025
DOI 10.1111/all.16580 PMID 40346988 3 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Phenotypes of Food Allergies in Patients with Atopic Dermatitis Aged Under 24 Months: A Multicenter Study
Diagnostics, 2025
DOI 10.3390/diagnostics15202656 PMID 41153328 1 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Clinical and Genetic Characteristics of Global Cohort of 132 Individuals with Janus Kinase-3 Deficiency
Journal of Human Immunity, 2025
DOI 10.70962/cis2025abstract.169 Açık erişimli tam metinKaynak: OpenAlex
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Health-related quality of life in pediatric patients with asthma receiving medical treatment and immunotherapy
Gazzetta Medica Italiana Archivio per le Scienze Mediche, 2025
DOI 10.23736/s0393-3660.24.05654-7 Kaynak: OpenAlex
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Malignancies and Lymphoproliferations in Children With Primary Immune Deficiency—A Single-center Experience
Journal of Pediatric Hematology/Oncology, 2024
DOI 10.1097/mph.0000000000002817 PMID 38277623 1 atıf (Europe PMC) Kaynak: OpenAlex
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Salmonella Osteomyelitis Due to IRAK-4 Deficiency
Journal of Pediatric Hematology/Oncology, 2024
DOI 10.1097/mph.0000000000002887 PMID 38857180 Kaynak: OpenAlex
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MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort
The Journal of Allergy and Clinical Immunology In Practice, 2024
DOI 10.1016/j.jaip.2024.06.046 PMID 38996837 7 atıf (Europe PMC) Kaynak: OpenAlex
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Life quality, depression, and anxiety levels in parents of children with primary immunodeficiency
Pediatric Allergy and Immunology, 2024
DOI 10.1111/pai.14068 PMID 38284917 5 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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Single Mutation different Clinical Findings: IGLL1 Defect
Iranian Journal of Allergy Asthma and Immunology, 2024
DOI 10.18502/ijaai.v23i4.16218 PMID 39549297 2 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Successful Oral Acetazolamide Desensitization in a Pediatric Patient with Anaphylaxis
Asthma Allergy Immunology, 2024
DOI 10.21911/aai.2024.464 1 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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A Novel Homozygous Six Base Pair Deletion Found in the NFATC2 Gene in a Patient with EBV-Associated Lymphoproliferation
Journal of clinical immunology, 2024
DOI 10.1007/s10875-024-01675-z PMID 38427060 2 atıf (Europe PMC) Açık erişimli tam metinKaynak: Europe PMC
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Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye
Journal of Clinical Immunology, 2024
DOI 10.1007/s10875-024-01759-w PMID 38954121 14 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Expanding the phenotypic and genotypic characteristics of trichohepatoenteric syndrome: a report of eight patients from five unrelated families
Molecular Biology Reports, 2024
DOI 10.1007/s11033-024-09656-6 PMID 38874671 2 atıf (OpenAlex) Kaynak: OpenAlex
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Late-Onset Concurrent Infection of Vaccine Strain VZV and HSV-1 after Varicella Vaccination in a Child with Natural killer T Cell Deficiency
Journal of Pediatric Infectious Diseases, 2024
DOI 10.1055/s-0044-1786997 1 atıf (OpenAlex) Kaynak: OpenAlex
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A Rare Clinical Finding in Ataxia Telangiectasia: Granulomatous Skin Lesion
Turkish Archives of Pediatrics, 2024
DOI 10.5152/turkarchpediatr.2024.23283 PMID 38813666 1 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Hepatic Veno-Occlusive Disease with Immunodeficiency (VODI): A Case Report and Review of Literature
Journal of Molecular Virology and Immunology, 2024
DOI 10.46683/jmvi.2024.87 Açık erişimli tam metinKaynak: OpenAlex
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Comparison of Diagnostic Efficacy of Lancet, Multi-Head Applicator, and Specific Immunoglobulin E in Allergy Testing
Çocuk Dergisi / Journal of Child, 2023
DOI 10.26650/jchild.2023.1341124 Açık erişimli tam metinKaynak: OpenAlex
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Neurologic Status of Patients with Purine Nucleoside Phosphorylase Deficiency Before and After Hematopoetic Stem Cell Transplantation
Journal of Clinical Immunology, 2023
DOI 10.1007/s10875-023-01585-6 PMID 37726596 4 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency
Journal of Allergy and Clinical Immunology, 2023
DOI 10.1016/j.jaci.2023.08.004 PMID 37595759 61 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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A novel homozygous frameshift CCNO variant presenting with primary ciliary dyskinesia and selective IgM deficiency
Pediatric Pulmonology, 2023
DOI 10.1002/ppul.26607 PMID 37503872 3 atıf (Europe PMC) Açık erişimli tam metinKaynak: ORCID
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The Course of COVID-19 in a Patient with Congenital Neutropenia: A Case Report
Bagcilar Medical Bulletin, 2023
DOI 10.4274/bmb.galenos.2022.2022-07-066 Açık erişimli tam metinKaynak: ORCID
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A Case Diagnosed with Chronic Granulomatous Disease Presenting with Dactylitis
Bagcilar Medical Bulletin, 2023
DOI 10.4274/bmb.galenos.2023.2023-08-070 Açık erişimli tam metinKaynak: ORCID
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Risk factors predisposing children to food allergies
Allergologia et Immunopathologia, 2023
DOI 10.15586/aei.v51i5.937 PMID 37695233 3 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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DRESS Syndrome due to Carbamazepine Use in A Drug-Addicted Adolescent
Asthma Allergy Immunology, 2023
DOI 10.21911/aai.004 3 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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A Rare Cause of Congenital Neutropenia: SRP54 Variant
Asthma Allergy Immunology, 2023
DOI 10.21911/aai.122 1 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants
Scandinavian Journal of Immunology, 2022
DOI 10.1111/sji.13163 PMID 35303369 6 atıf (Europe PMC) Kaynak: OpenAlex
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Comparing the levels of CTLA-4-dependent biological defects in patients with LRBA deficiency and CTLA-4 insufficiency
Allergy, 2022
DOI 10.1111/all.15331 PMID 35491430 26 atıf (Europe PMC) Açık erişimli tam metinKaynak: Europe PMC
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Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency
Journal of Clinical Immunology, 2022
DOI 10.1007/s10875-021-01191-4 PMID 35079916 35 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Dupilumab combined with a short-term narrowband- ultraviolet B phototherapy in a pediatric case of severe atopic dermatitis
TURKDERM, 2022
DOI 10.4274/turkderm.galenos.2021.67424 1 atıf (OpenAlex) Açık erişimli tam metinKaynak: OpenAlex
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Lovebird-induced Aspergillus Infection in a Child with Chronic Granulomatous Disease
Cam and Sakura Medical Journal, 2022
DOI 10.4274/csmedj.galenos.2022.2022-1-1 Açık erişimli tam metinKaynak: OpenAlex
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Asthma and allergic diseases are not risk factors for hospitalization in children with coronavirus disease 2019
Annals of Allergy Asthma & Immunology, 2021
DOI 10.1016/j.anai.2021.01.018 PMID 33493639 34 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex