Bilimsel çalışmalar
Dr. Ezgi Topyıldız
29 yayın. Her yayının yanında bilginin kaynağı yazar.
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Minimal Wheal Reactions on Skin Prick Testing Predict Future Aeroallergen Sensitization in Children: A Longitudinal Study
The Journal of Pediatric Research, 2026
DOI 10.4274/jpr.galenos.2026.04820 Kaynak: OpenAlex
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Timing of cow’s milk oral immunotherapy and adverse reactions in children: A 15-year experience
Annals of Allergy Asthma & Immunology, 2026
DOI 10.1016/j.anai.2026.01.016 PMID 41616970 1 atıf (Europe PMC) Kaynak: OpenAlex
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B cells, autoimmunity, and innate immunity in 22q11.2 deletion syndrome: a two-center study and review of the literature
Central European Journal of Immunology, 2026
DOI 10.5114/ceji/208683 PMID 42677014 Açık erişimli tam metinKaynak: OpenAlex
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Unclassified Inborn Errors of Immunity Patients without any Pathogenic Variant in Targeted Next-Generation Sequencing: Long-Term Follow-up and Whole Exome Sequencing Results
Journal of Clinical Immunology, 2026
DOI 10.1007/s10875-026-02007-z PMID 41917218 Açık erişimli tam metinKaynak: OpenAlex
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Reply to “Asymptomatic esophageal eosinophilia in oral immunotherapy: context and clinical application”
The Journal of Allergy and Clinical Immunology In Practice, 2026
DOI 10.1016/j.jaip.2026.02.017 PMID 41956624 Kaynak: OpenAlex
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Exploring the association between interleukin-27 and Dermatophagoides-specific IgE responses in children with allergic rhinitis and asthma
Allergologia et Immunopathologia, 2026
DOI 10.15586/aei.v54i3.1564 PMID 42115790 Kaynak: OpenAlex
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Short‐term early exposure to cow's milk formula increases the risk of cow's milk allergy: A critical window in early life
Pediatric Allergy and Immunology, 2026
DOI 10.1111/pai.70497 PMID 42830732 Kaynak: OpenAlex
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Aeroallergen Sensitivity Profile in Children in Hatay Province: A Single-Center Cross-Sectional Study
Çocuk Dergisi / Journal of Child, 2026
DOI 10.26650/jchild.2026.1932158 Kaynak: OpenAlex
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Endoscopic Evaluation of Patients With Food Allergy for Eosinophilic Esophagitis Before Oral Immunotherapy
The Journal of Allergy and Clinical Immunology In Practice, 2025
DOI 10.1016/j.jaip.2025.08.029 PMID 40930402 2 atıf (Europe PMC) 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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Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients
The Journal of Pediatric Research, 2024
DOI 10.4274/jpr.galenos.2024.09735 Kaynak: OpenAlex
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Facilitated Subcutaneous Immunoglobulin Treatment Increases the Quality of Life and Decreases the Number of Infections and Hospitalizations in Children with Primary Immunodeficiencies
International Archives of Allergy and Immunology, 2024
DOI 10.1159/000534900 PMID 38246144 2 atıf (Europe PMC) Kaynak: OpenAlex
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Immune Responses to Respiratory Infections
Comprehensive ENT, 2024
DOI 10.1007/978-3-031-74853-0_7 Kaynak: OpenAlex
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Factors effecting natural course of egg allergy
European Annals of Allergy and Clinical Immunology, 2023
DOI 10.23822/eurannaci.1764-1489.287 PMID 36891735 1 atıf (Europe PMC) Kaynak: OpenAlex
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Successful treatment of post-pericardiotomy syndrome via C1 inhibitor replacement therapy in a hereditary angioedema patient with Marfan syndrome
The Turkish Journal of Pediatrics, 2023
DOI 10.24953/turkjped.2022.637 PMID 37114700 1 atıf (Europe PMC) Kaynak: OpenAlex
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Autoimmune Cytopenias Are Highly Associated with Inborn Errors of Immunity and They May Be the Initial Presentations in Cases without Severe Infections
International Archives of Allergy and Immunology, 2023
DOI 10.1159/000535258 PMID 38154455 5 atıf (Europe PMC) Kaynak: OpenAlex
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Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experience
Immunologic Research, 2023
DOI 10.1007/s12026-023-09426-9 PMID 37840117 5 atıf (Europe PMC) Kaynak: OpenAlex
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Dual Diagnosis of Trichohepatoenteric Syndrome and Lipoid Proteinosis in a Turkish Child
Molecular Syndromology, 2023
DOI 10.1159/000531408 PMID 38058753 3 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Transient hypogammaglobulinemia of infancy and unclassified syndromic immunodeficiencies are highly common in oesophageal atresia patients
Scandinavian Journal of Immunology, 2023
DOI 10.1111/sji.13338 PMID 38981850 Kaynak: OpenAlex
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An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission
Case Reports in Immunology, 2023
DOI 10.1155/2023/2363760 PMID 37144156 2 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Alterations in B and NK cells highly correlate with disease severity in children with COVID-19
TURKISH JOURNAL OF MEDICAL SCIENCES, 2023
DOI 10.55730/1300-0144.5686 PMID 38813014 1 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Effectiveness and adverse reactions to subcutaneous immunotherapy in children with allergic rhinitis/asthma
International Journal of Pediatric Otorhinolaryngology, 2022
DOI 10.1016/j.ijporl.2022.111292 PMID 36007303 11 atıf (Europe PMC) Kaynak: OpenAlex
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Could Age and Oral Challenge Outcomes Identify High-Risk Patients During Cow's Milk Oral Immunotherapy?
Pediatric Allergy Immunology and Pulmonology, 2022
DOI 10.1089/ped.2022.0003 PMID 35675663 Kaynak: OpenAlex
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A Novel BLNK Gene Mutation in a Four-Year-Old Child Who Presented with Late Onset of Severe Infections and High IgM Levels and Diagnosed and Followed as X-Linked Agammaglobulinemia for Two Years
Case Reports in Immunology, 2022
DOI 10.1155/2022/7313009 PMID 35719418 Açık erişimli tam metinKaynak: OpenAlex
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Besin Alerjilerinin Tedavisinde Spesifik İmmünoterapi
2021
Kaynak: OpenAlex
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Consensus Middle East and North Africa Registry on Inborn Errors of Immunity
Journal of Clinical Immunology, 2021
DOI 10.1007/s10875-021-01053-z PMID 34052995 70 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA‐2; PLCG2): Striking clinical phenotypic overlap and difference
Clinical Case Reports, 2021
DOI 10.1002/ccr3.3934 PMID 33936634 12 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex
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A Novel Homozygous TRNT1 Mutation in a Child With an Early Diagnosis of Common Variable Immunodeficiency Leading to Mild Hypogammaglobulinemia and Hemolytic Anemia
Journal of Pediatric Hematology/Oncology, 2021
DOI 10.1097/mph.0000000000002101 PMID 33843817 10 atıf (Europe PMC) Kaynak: OpenAlex
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Erratum: X-linked agammaglobulinemia: investigation of clinical and laboratory findings, novel gene mutations and prevention of infective complications in long-term follow-up.
Europe PMC (PubMed Central), 2021
PMID 33815962 2 atıf (Europe PMC) Açık erişimli tam metinKaynak: OpenAlex