Prof. DENİZ NAZİRE ÇAĞDAŞ AYVAZ

Publication Network

Journal articles indexed in SCI, SSCI, and AHCI

Comprehensive αβ T-Cell Receptor Repertoire Analysis Reveals a Unique CD8+ TCR Landscape in DOCK8-Deficient Patients.

Bozkurt C., Cildir G., Aba U., Erdogan R. K., Warnock N. I., Kok C. H., et al.

Allergy , 2025 (SCI-Expanded)

Amyloidosis in Human Inborn Errors of Immunity Predicts Poor Prognosis.

Aytekin E. S., Tagiyev A., Silleli O., Samur İ., Demirel F., Esenboğa S., et al.

Journal of clinical immunology , vol.45, no.1, pp.88, 2025 (SCI-Expanded)

A patient with RFX5 variant causing an expression defect in both HLA ABC and HLA DR.

Goktas S., Sonmez G., Şahin A., Çevik N. N., Caka C., Yaz İ., et al.

Immunologic research , vol.73, no.1, pp.72, 2025 (SCI-Expanded) Sustainable Development

Genetic Variants in Early-Onset Inflammatory Bowel Disease: Monogenic Causes and Clinical Implications

Demirtas Guner D., Bildik H. N., Demir H., Çağdaş Ayvaz D. N., Saltik Temizel I. N., Ozgul R. K., et al.

CHILDREN (BASEL) , vol.12, no.5, pp.1-8, 2025 (SCI-Expanded) Sustainable Development

Five Patients with Two Novel Homozygous Variants in CD3 Subunits and Comprehensive Review of the Literature.

Sonmez G., Kazancıoglu A., Yazarkan Y., Tenekeci A. K., Yaz İ., Esenboga S., et al.

The journal of allergy and clinical immunology. In practice , 2025 (SCI-Expanded)

Challenge in a Malrotation Case: Presentation Mimicking Severe Combined Immunodeficiency.

Fathelbab J., Cagdas D. N., Emet D. C., Oguz B., Andiran F.

Journal of paediatrics and child health , 2025 (SCI-Expanded)

Phenotypic diversity in NAXE mutations.

Solmaz I., Yalnızoğlu D., Dursun A., Çıkı K., Akar H. T., Özgül R. K., et al.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology , 2025 (SCI-Expanded)

Recurrent eosinophilia with a novel homozygous ARPC1B mutation.

Sonmez G., Ulum B., Tenekeci A. K., Caka C., Şahin A., Kazancıoğlu A., et al.

Frontiers of medicine , vol.19, no.1, pp.174-180, 2025 (SCI-Expanded)

Human FCHO1 deficiency: review of the literature and additional two cases.

Özdemiral C., Yaz İ., Esenboga S., Nabiyeva Cevik N., Bildik H. N., Kilic M., et al.

Clinical and experimental immunology , vol.219, no.1, 2025 (SCI-Expanded)

Inborn errors of immunity-related immunological mechanisms and pharmacological therapy alternatives in periodontitis.

Nabiyeva Çevik N., Berker E., Tezcan I., Cagdas D. N.

Clinical and experimental immunology , vol.219, no.1, 2025 (SCI-Expanded)

Rare Case of Recurrent Salmonella Typhimurium Meningitis in a 55-day-old Infant: Importance of Immunodeficiency Susceptibility.

Uzuner S., Turel O., Yozgat C. Y., Erenberk U., Ayvaz D. N., Boisson-Dupuis S.

Klinische Padiatrie , vol.237, no.1, pp.50-52, 2025 (SCI-Expanded)

Respiratory system evaluation of adult primary immunodeficiency patients: a tertiary care center experience

Kaya S. B., Çakmak M. E., Bostan Ö. C., Damadoğlu E., Karakaya G., Kalyoncu A. F., et al.

POSTEÓPY HIGIENY I MEDYCYNY DOSÂWIADCZALNEJ , vol.79, no.1, pp.1-3, 2025 (SCI-Expanded)

Characteristics of patients with low serum IgE levels and selective IgE deficiency: Data from an immunodeficiency referral center

Ünsal H., Ekinci A., Aliyeva G., Bildik H. N., Esenboğa S., Çağdaş Ayvaz D. N.

CLINICAL IMMUNOLOGY , vol.1, no.1, pp.1-7, 2025 (SCI-Expanded) Sustainable Development

Comparative analysis of protein expression profiles with genotypes in the diagnosis of Inborn Errors of Immunity.

Oskay Halacli S., Cagdas D. N., Esenboga S., Inan D., Yaz İ., Cicek B., et al.

Scandinavian journal of clinical and laboratory investigation , pp.1-10, 2024 (SCI-Expanded) Sustainable Development

A large cohort from an immunology reference center and an algorithm for the follow-up of chronic neutropenia.

Caka C., Ergenoğlu D. N., Sinanoğlu N., Maslak I. C., Bildik H. N., Çiçek B., et al.

Journal of clinical immunology , vol.45, no.1, pp.38, 2024 (SCI-Expanded)

Human DNA-dependent protein kinase catalytic subunit deficiency: a comprehensive review and update.

Adelon J., Abolhassani H., Esenboga S., Fouyssac F., Cagdas D. N., Tezcan I., et al.

The Journal of allergy and clinical immunology , vol.154, pp.1300-1312, 2024 (SCI-Expanded)

Frequencies of Human Leukocyte Antigen Alleles in Turkish Children with Kawasaki Disease

Teke T. A., TAN Ç., Aydin Z. G. G., Kaman A., ÇİÇEK B., Oz F. N., et al.

JOURNAL OF PEDIATRIC INFECTIOUS DISEASES , no.06, pp.309-316, 2024 (SCI-Expanded)

Newborn screening for SCID: the very first prospective pilot study from Türkiye

Haskologlu S., Kocak S., Tufan L. S., Aksoy F. E., Bastug D., Oner D. A., et al.

FRONTIERS IN IMMUNOLOGY , vol.15, pp.1-12, 2024 (SCI-Expanded) Sustainable Development

A single center experience on PI3K/AKT/MTOR signaling defects: Towards pathogenicity assessment for four novel defects.

Bildik H. N., Esenboga S., Halaclı S., Karaatmaca B., Aytekin E. S., Nabiyeva N., et al.

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology , vol.35, no.9, 2024 (SCI-Expanded)

Evaluation of patients with Primary Ciliary Dyskinesia in terms of humoral immunodeficiency

Buyuksahin H. N., EMİRALİOĞLU ORDUKAYA N., CAKA C., ESENBOĞA S., ÇAĞDAŞ AYVAZ D. N., ATAN R., et al.

EUROPEAN RESPIRATORY JOURNAL , 2024 (SCI-Expanded)

Regulation of MYC by CARD14 in human epithelium is a determinant of epidermal homeostasis and disease.

DeVore S. B., Schuetz M., Alvey L., Lujan H., Ochayon D. E., Williams L., et al.

Cell reports , vol.43, no.8, pp.114589, 2024 (SCI-Expanded)

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.

Erman B., Aba U., Ipsir C., Pehlivan D., Aytekin C., Cildir G., et al.

Journal of clinical immunology , vol.44, no.7, pp.157, 2024 (SCI-Expanded)

Indolent B-cell non-Hodgkin lymphomas in children: high association with inborn errors of immunity

Kurucu N., Kutluk T., Sağlam A., Çağdaş Ayvaz D. N., Haliloğlu M., Salancı B. V., et al.

LEUKEMIA AND LYMPHOMA , vol.1, no.1, pp.1-3, 2024 (SCI-Expanded)

Inborn Errors of Immunity in Adults with Autoimmune Liver Diseases.

Ayar Ş. N., Aytekin E. S., Şimşek C., Dağ O., Çağdaş D. N., Balaban Y. H.

The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology , vol.35, no.7, pp.560-567, 2024 (SCI-Expanded) Sustainable Development

Clinical efficacy of SARS-CoV-2 Omicron-neutralizing antibodies in immunoglobulin preparations for the treatment of agammaglobulinemia in patients with primary antibody deficiency.

Karbiener M., Kindle G., Meyts I., Seppänen M. R. J., Candotti F., Kamieniak M., et al.

Journal of medical virology , vol.96, no.6, 2024 (SCI-Expanded)

Ocular Changes and Tear Cytokines in Individuals with Low Serum Vitamin D Levels: A Cross-Sectional, Controlled Study.

Çalık Başaran N., Kırağı D., Tan Ç., Özışık L., Çağdaş Ayvaz D. N., Kocabeyoğlu S., et al.

OCULAR IMMUNOLOGY AND INFLAMMATION , vol.32, no.3, pp.287-294, 2024 (SCI-Expanded)

Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre.

Karaatmaca B., Cagdas D. N., Esenboga S., Erman B., Tan C., Ozgur T. T., et al.

Clinical and experimental immunology , vol.215, no.2, pp.160-176, 2024 (SCI-Expanded)

The spectrum of side effects associated with COVID-19 vaccines in patients with inborn errors of immunity.

Özdemiral C., Cevik N. N., Yavuz G., Gormez O., Zengin A. B., Esenboga S., et al.

Clinical immunology (Orlando, Fla.) , vol.259, pp.109878, 2024 (SCI-Expanded)

GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway.

Park A. Y., Leney-Greene M., Lynberg M., Gabrielski J. Q., Xu X., Schwarz B., et al.

Nature immunology , vol.25, pp.282-293, 2024 (SCI-Expanded)

JAK inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID/EBMT-IEWP retrospective study.

Fischer M., Olbrich P., Hadjadj J., Aumann V., Bakhtiar S., Barlogis V., et al.

The Journal of allergy and clinical immunology , vol.153, no.1, 2024 (SCI-Expanded)

A large single-center cohort of bare lymphocyte syndrome: Immunological and genetic features in Turkey

Ünsal H., Caka C., Bildik H. N., Esenboğa S., Kupesiz A., Kuşkonmaz B. B., et al.

Scandinavian Journal of Immunology , vol.99, no.1, 2024 (SCI-Expanded) Sustainable Development

COVID-19-related multiple inflammatory syndrome-C and pulmonary embolism in Aicardi-Goutries syndrome.

Çevik N. N., Aytekin E., Esenboğa S., Özbek B., Aytaç Ş. S., Özen S., et al.

Pediatric pulmonology , vol.58, pp.3326-3329, 2023 (SCI-Expanded)

APECED and the place of AIRE in the puzzle of the immune network associated with autoimmunity

Aytekin E. S., Çağdaş Ayvaz D. N.

Scandinavian Journal of Immunology , vol.98, no.2, 2023 (SCI-Expanded) Sustainable Development

Clinical and Osteopetrosis-Like Radiological Findings in Patients with Leukocyte Adhesion Deficiency Type III.

Kahraman A. B., Yaz İ., Gocmen R., Aytac Ş. S., Metin A., Kilic S. S., et al.

Journal of clinical immunology , vol.43, no.6, pp.1250-1258, 2023 (SCI-Expanded)

Eosinophilia in children: characteristics, etiology and diagnostic algorithm.

Cetinkaya P. G., Aytekin E. S., Esenboga S., Cagdas D. N., Sahiner Ü. M., Sekerel B. E., et al.

European journal of pediatrics , vol.182, no.6, pp.2833-2842, 2023 (SCI-Expanded) Sustainable Development

Cutaneous findings in Inborn Errors of Immunity: An immunologist`s perspective

Çağdaş Ayvaz D. N., Ayasun R., Gulseren D., Sanal O., Tezcan I.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY: IN PRACTICE , vol.1, no.1, pp.1-10, 2023 (SCI-Expanded) Sustainable Development

Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.

Lévy R., Gothe F., Momenilandi M., Magg T., Materna M., Peters P., et al.

The Journal of experimental medicine , vol.220, no.2, 2023 (SCI-Expanded)

Orai1 defect in a patient with disseminated cmv infection and severe hypotonia

Deveci K., Esenboğa S., Bildik H. N., Ocak M., Gülşen H. H., Ertuğrul İ., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.65, no.4, pp.698-703, 2023 (SCI-Expanded)

A novel variant in severe disease of DADA2: involving vasculitic and haematologic features

AYAN G., Yagiz B., ÇINAR O. E., ÇAĞDAŞ AYVAZ D. N., ÖZBEK D. A., TUNCER A., et al.

SCANDINAVIAN JOURNAL OF RHEUMATOLOGY , vol.52, no.1, pp.93-95, 2023 (SCI-Expanded)

D-dimer elevation during tranexamic acid therapyand the debate on the therapeutic approach in hereditaryangioedema type I

Özdemiral C., Cagdas D. N.

ALERGOLOGIA POLSKA-POLISH JOURNAL OF ALLERGOLOGY , vol.10, no.1, pp.63-67, 2023 (SCI-Expanded) Sustainable Development

Dock8 deficiency with hypereosinophilia and the syndrome of inappropriate antidiuretic hormone secretion during herpes infection

Mete Yeşil A., Kayaoğlu B., Gül E., Gönç N., Özön A., Tezcan İ., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.65, no.3, pp.536-541, 2023 (SCI-Expanded) Sustainable Development

The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity.

Baris S., Abolhassani H., Massaad M. J., Al-Nesf M., Chavoshzadeh Z., Keles S., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY: IN PRACTICE , vol.11, no.1, pp.158-180, 2023 (SCI-Expanded) Sustainable Development

High Inborn Errors of Immunity Risk in Patients with Granuloma

Süleyman M., Serin O., Koçali B., Orhan D., Yalçın E. E., Özçelik U., et al.

Journal of Clinical Immunology , vol.42, no.8, pp.1795-1809, 2022 (SCI-Expanded)

A single-center study points to diverse features and outcome in patients with Hyperimmunoglobulin M Syndrome and Class- Switch Recombination defects

Akarsu A., Halaçlı S., Tan Ç., Kuşkonmaz B. B., Küpesiz A., Çetinkaya D., et al.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY , vol.96, no.5, 2022 (SCI-Expanded)

Childhood-onset Takayasu arteritis and immunodeficiency: case-based review.

Sener S., Basaran O., Batu E. D., Atalay E., Esenboga S., Cagdas D. N., et al.

Clinical rheumatology , vol.41, no.9, pp.2883-2892, 2022 (SCI-Expanded) Sustainable Development

A Rare Central Nervous System Involvement Due to CTLA-4 Gene Defect

Rovshanov S., GÖÇMEN R., BARIŞTA İ., ÇAĞDAŞ AYVAZ D. N., ÜNER A., Çilingir V., et al.

NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY , vol.59, no.3, pp.248-252, 2022 (SCI-Expanded)

Antimycobacterial prophylaxis regarding Bacillus Calmette-Guérin -associated complications in children with primary immunodeficiency

Ozsezen B., Yalçın E., Ademhan Tural D., Sunman B., Nayır Buyuksahin H., Guzelkas İ., et al.

Respiratory Medicine , vol.200, 2022 (SCI-Expanded)

The clinical and demographical characteristics of Turkish pediatric lymphedema patients: a multicenter study.

Borman P., Balcan A., Eyigör S., Coşkun E., Ayhan F., Çakıt B. D., et al.

Turkish journal of medical sciences , vol.52, no.4, pp.1139-1147, 2022 (SCI-Expanded)

Clinical, Laboratory Features and Clinical Courses of Patients with Wiskott Aldrich Syndrome and X-linked Thrombocytopenia-A single center study.

Bildik H. N., Cagdas D. N., Ozturk Kura A., Oskay Halacli S., Sanal O., Tezcan I.

Immunological investigations , vol.51, no.5, pp.1272-1283, 2022 (SCI-Expanded)

Central Nervous System Vasculitis in Primary Immune Deficiency

Sayici B. U., Oz S., Gocmen R., Tezcan F., ÇAĞDAŞ AYVAZ D. N., Esenboga S., et al.

EUROPEAN JOURNAL OF NEUROLOGY , vol.29, pp.556, 2022 (SCI-Expanded)

First allogeneic hematopoietic stem cell transplantation in RASGRP1 deficiency: long-term follow-up.

Kuskonmaz B. B., Ayvaz D. N., Okur F. V., Aydın B., Tezcan I., Uckan Cetinkaya D.

Bone marrow transplantation , vol.57, pp.1210-1212, 2022 (SCI-Expanded)

Cytokine profile in serum and gingival crevicular fluid of children with inflammatory bowel disease: A case-control study

Acar B., Gümüş E., Özcan-Bulut S., Özşin-Özler C., Boyraz M. S., Tan Ç., et al.

JOURNAL OF PERIODONTOLOGY , vol.93, no.7, pp.1048-1059, 2022 (SCI-Expanded)

GIMAP6 regulates autophagy, immune competence, and inflammation in mice and humans.

Yao Y., Du Jiang P., Chao B. N., Cagdas D. N., Kubo S., Balasubramaniyam A., et al.

The Journal of experimental medicine , vol.219, no.6, 2022 (SCI-Expanded)

Long Term Follow-Up of the Patients with Severe Combined Immunodeficiency After Hematopoietic Stem Cell Transplantation: A Single-Center Study.

Demirtas D., Cagdas D. N., Turul Ozgur T., Kuskonmaz B. B., Uckan Cetinkaya D., Sanal O., et al.

Immunological investigations , vol.51, no.4, pp.739-747, 2022 (SCI-Expanded)

Association between idiopathic thrombocytopenic purpura and HLA genotype in Turkish patients

Arbag S. N., Guleryuz G. O., TEZCAN F. İ., ÇAĞDAŞ AYVAZ D. N., ÖZMEN F.

HLA , vol.99, no.5, pp.509, 2022 (SCI-Expanded)

TMC8 mutation in a Turkish family with epidermodysplasia verruciformis including laryngeal papilloma and recurrent skin carcinoma.

Esenboga S., Cagdas D. N., Alkanat N. E., Güler Tezel G., Ersoy Evans S., Boztug K., et al.

Journal of cosmetic dermatology , vol.21, no.5, pp.2263-2267, 2022 (SCI-Expanded)

Adenosine Deaminase Type II Deficiency: Severe Chronic Neutropenia, Lymphoid Infiltration in Bone Marrow, and Inflammatory Features.

SÜLEYMAN M., TAN Ç., ÜNER A., Inkaya C., Aytac Ş. S., BÜYÜKAŞIK Y., et al.

Immunological investigations , vol.51, no.3, pp.558-566, 2022 (SCI-Expanded)

Combined immunodeficiency due to purine nucleoside phosphorylase deficiency: Outcome of three patients

Torun B., Bilgin A., ORHAN D., GÖÇMEN R., KILIÇ GÜLTEKİN S. Ş., KUŞKONMAZ B. B., et al.

European Journal of Medical Genetics , vol.65, no.3, 2022 (SCI-Expanded)

STK4 deficiency and EBV-associated lymphoproliferative disorders, emphasis on histomorphology, and review of literature.

Saglam A., Cagdas D. N., Aydin B., Keles S., Reisli I., Arslankoz S., et al.

Virchows Archiv : an international journal of pathology , vol.480, no.2, pp.393-401, 2022 (SCI-Expanded)

Multicentric Castleman disease in a DOCK8-deficient patient with Orf virus infection.

Aydin Goker E. T., Cagdas D. N., Bajin I. Y., Kukul M. G., Aytekin E. S., Orhan D., et al.

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology , vol.33, no.1, 2022 (SCI-Expanded)

Double Trouble in an Adult Patient with UNC13D mutation: EBV-Associated Lymphoproliferation and Kaposi Sarcoma

Nabiyeva N., Esenboga S., Ozdemir E., Berber I., Yaz İ., Bildik H. N., et al.

UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI , vol.32, no.4, pp.246-250, 2022 (SCI-Expanded)

Nutritional status of children with primary immunodeficiency: A single center experience

Karhan A. N., Esenboğa S., Gümüş E., Karaatmaca B., Cagdas D. N., Demir H., et al.

PEDIATRICS INTERNATIONAL , vol.64, no.1, 2022 (SCI-Expanded) Sustainable Development

Respiratory system findings in pediatric patients with primary immunodeficiency

Esenboga S., Oguz B., Cagdas D. N., Karaatmaca B., Emiralioglu N., Yalcin E., et al.

Pediatric Pulmonology , vol.56, no.12, pp.4011-4019, 2021 (SCI-Expanded)

Hematopoietic stem cell transplantation complicated with EBV associated hemophagocytic lymphohistiocytosis in a patient with DOCK2 deficiency

Aytekin E. S., ÇAĞDAŞ AYVAZ D. N., TAN Ç., Cavdarli B., Bilgic I., Tezcan I.

TURKISH JOURNAL OF PEDIATRICS , vol.63, no.6, pp.1072-1077, 2021 (SCI-Expanded)

Expression of HLA class I and class II genes in patients with multiple skin warts

Gülseren D., Tan Ç., Yaz İ., Özbek B., Çağdaş D. N., Tezcan İ.

EXPERIMENTAL DERMATOLOGY , vol.30, no.11, pp.1642-1649, 2021 (SCI-Expanded) Sustainable Development

EBV Associated Smooth Muscle Tumors in Children with Primary Immunodeficiency Disorders

Bajin I. Y., KÖSEMEHMETOĞLU K., ORHAN D., ÇAĞDAŞ AYVAZ D. N., Kutluk T.

PEDIATRIC BLOOD & CANCER , vol.68, 2021 (SCI-Expanded)

Maternofetal Transfusion, Maternal Chimerism, and Maternal Engraftment: A Mystery in Health and Disease

ÇAĞDAŞ AYVAZ D. N.

Journal of Allergy and Clinical Immunology: In Practice , vol.9, no.11, pp.4154-4155, 2021 (SCI-Expanded)

Differential diagnosis of primary immunodeficiency in patients with BCGitis and BCGosis: A single-centre study

SOYAK AYTEKİN E., KESKİN A., TAN Ç., Yalcin E., DOĞRU ERSÖZ D., Ozcelik U., et al.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY , vol.94, no.4, 2021 (SCI-Expanded) Sustainable Development

Clinical and laboratory findings in patients with leukocyte adhesion deficiency type I: A multicenter study in Turkey

Yaz İ., Ozbek B., Bildik H. N., Tan C., Oskay Halacli S., Soyak Aytekin E., et al.

CLINICAL AND EXPERIMENTAL IMMUNOLOGY , vol.206, no.1, pp.47-55, 2021 (SCI-Expanded)

Diversity in Serine/Threonine Protein Kinase-4 Deficiency and Review of the Literature

Cagdas D. N., Halacli S., Tan C., Esenboğa S., Karaatmaca B., Cetinkaya P. G., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE , vol.9, no.10, pp.3752-3770, 2021 (SCI-Expanded)

COVID-19 in Patients with Primary Immunodeficiency

Esenboga S., Ocak M., Akarsu A., Bildik H. N., Cagdas D. N., Iskit A. T., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , vol.41, no.7, pp.1515-1522, 2021 (SCI-Expanded)

Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child

Ogishi M., Yang R., Aytekin C., Langlais D., Bourgey M., Khan T., et al.

NATURE MEDICINE , vol.27, no.9, pp.1646-1680, 2021 (SCI-Expanded) Sustainable Development

Hematologically important mutations: X-linked chronic granulomatous disease (fourth update)

Roos D., van Leeuwen K., Hsu A. P., Priel D. L., Begtrup A., Brandon R., et al.

BLOOD CELLS MOLECULES AND DISEASES , vol.90, 2021 (SCI-Expanded)

Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency

Cagdas D. N., Mayr D., Baris S., Worley L., Langley D. B., Metin A., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , vol.41, no.6, pp.1272-1290, 2021 (SCI-Expanded)

The imbalance of the circulating regulatory B cell subsets in patients with primary immunodeficiencies

Halacli S., Inan D., BİLDİK H. N., AKARSU A., Kahveci M., Ozbek B., et al.

EUROPEAN JOURNAL OF IMMUNOLOGY , vol.51, pp.83, 2021 (SCI-Expanded)

Selective IgM deficiency: Follow-up and outcome

Caka C., Cimen O., Kahyaoğlu P., Tezcan İ., Cagdas D. N.

PEDIATRIC ALLERGY AND IMMUNOLOGY , vol.32, no.6, pp.1327-1334, 2021 (SCI-Expanded)

Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update).

Roos D., van Leeuwen K., Hsu A. P., Priel D. L., Begtrup A., Brandon R., et al.

Blood cells, molecules & diseases , vol.92, pp.102596, 2021 (SCI-Expanded)

Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience

Akar H. T., Esenboga S., Cagdas D. N., Halacli S., Ozbek B., van Leeuwen K., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , vol.41, no.5, pp.992-1003, 2021 (SCI-Expanded)

Impact of Mannose-Binding Lectin 2 Gene Polymorphism on Disease Severity in Non-Cystic Fibrosis Bronchiectasis in Children

Dogru D., Polat E. S., Tan C., Tezcan I., YALÇIN S. S., Utine E., et al.

PEDIATRIC PULMONOLOGY , vol.56, 2021 (SCI-Expanded)

Frequency of HLA Class I and Class II Alleles in Patients with CVID from Turkey

Ozbek B., TAN Ç., Yaz I., KOŞUKCU C., Esenboga S., Cetinkaya P. G., et al.

IMMUNOLOGICAL INVESTIGATIONS , vol.50, no.4, pp.363-371, 2021 (SCI-Expanded)

Evaluation of periodontal status and cytokine/chemokine profile of GCF in patients with severe congenital neutropenia

Acar B., Ayvaz D. N., Tan Ç., Özbek B., Yaz İ., Yıldırım Y., et al.

ODONTOLOGY , vol.109, no.2, pp.474-482, 2021 (SCI-Expanded)

Convalescent Plasma and Hyperimmune Globulin Therapy in COVID-19.

Cagdas D. N.

Expert review of clinical immunology , vol.17, pp.309-315, 2021 (SCI-Expanded) Sustainable Development

Living the SARS-CoV-2 pandemic in Turkey.

Çağdaş D. N.

Nature immunology , vol.22, pp.260, 2021 (SCI-Expanded)

A Patient With AIRE Mutation Who Presented With Severe Diarrhea and Lung Abscess

Soyak A., Serin O., Cagdas D. N., Tan C., Aksu T., Unsal Y., et al.

Pediatric Infectious Disease Journal , vol.40, no.1, pp.66-69, 2021 (SCI-Expanded) Sustainable Development

First Allogeneic Hematopoietic Stem Cell Transplantation in RASGRP1 Deficieny

KUŞKONMAZ B. B., ÇAĞDAŞ AYVAZ D. N., OKUR F. V., Tezcan I., ÇETİNKAYA F. D.

BONE MARROW TRANSPLANTATION , vol.55, pp.653-654, 2020 (SCI-Expanded)

Mutational landscape of severe combined immunodeficiency patients from Turkey

Firtina S., Ng Y. Y., Ng O. H., KIYKIM A., ÖZEN A. O., ÖZEN A. O., et al.

INTERNATIONAL JOURNAL OF IMMUNOGENETICS , vol.47, no.6, pp.529-538, 2020 (SCI-Expanded)

Hemophagocytic Lymphohistiocytosis in Patients With Primary Immunodeficiency

Cetinkaya P. G., ÇAĞDAŞ AYVAZ D. N., GÜMRÜK F., Tezcan I.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , vol.42, no.6, 2020 (SCI-Expanded)

Three patients with glucose-6 phosphatase catalytic subunit 3 deficiency

Cetinkaya P. G., Cagdas D. N., Arikoglu T., GÜMRÜK F., Tezcan I.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.33, no.7, pp.957-961, 2020 (SCI-Expanded)

Recurrent skin abscesses in a female X-linked chronic granulomatous disease carrier

Altintas B., Cagdas D. N., van Leeuwen K., de Boer M., Roos D., Tezcan I.

JOURNAL OF COSMETIC DERMATOLOGY , vol.19, no.7, pp.1810-1812, 2020 (SCI-Expanded)

Recurrent Demyelinating Episodes as Sole Manifestation of Inherited CD59 Deficiency

SOLMAZ İ., Aytekin E. S., Cagdas D. N., TAN Ç., Tezcan I., GÖÇMEN R., et al.

NEUROPEDIATRICS , vol.51, no.3, pp.206-210, 2020 (SCI-Expanded)

Autoinflammation in addition to combined immunodeficiency: SLC29A3 gene defect

Cagdas D. N., Surucu N., TAN Ç., ÖZGÜL R. K., Akkaya-Ulum Y. Z., Aydinoglu A. T., et al.

MOLECULAR IMMUNOLOGY , vol.121, pp.28-37, 2020 (SCI-Expanded)

Impact of mannose-binding lectin 2 gene polymorphisms on disease severity in noncystic fibrosis bronchiectasis in children

Dogru D., Polat S. E., Tan Ç., Tezcan İ., Yalçın S. S., Utine E., et al.

PEDIATRIC PULMONOLOGY , vol.55, no.5, pp.1190-1198, 2020 (SCI-Expanded) Sustainable Development

A rare form of congenital neutropenia: VPS45 deficiency

Karaatmaca B., Cagdas D. N., TAN Ç., Aytac Ş. S., Ozbek B., ÜNER A., et al.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY , vol.91, no.5, 2020 (SCI-Expanded)

Lymphocyte Subgroups and KREC Numbers in Common Variable Immunodeficiency: A Single Center Study

Yaz I., Ozbek B., Ng Y. Y., Cetinkaya P. G., Halacli S., TAN Ç., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , vol.40, no.3, pp.494-502, 2020 (SCI-Expanded)

A clinical score to guide in decision making for monogenic type I IFNopathies.

Sönmez H., Karaaslan C., de J., Batu E., Anlar B., Sözeri B., et al.

Pediatric research , vol.87, no.4, pp.745-752, 2020 (SCI-Expanded)

A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2

Ozen S., Bilginer Y., Batu E., Taşkıran E., Özkara H. A., Ünal Ş., et al.

JOURNAL OF RHEUMATOLOGY , vol.47, no.1, pp.117-125, 2020 (SCI-Expanded)

In case of recurrent wheezing and bronchiolitis: Think again, it may be a primary immunodeficiency.

Ozbek B., Ayvaz D. N., Esenboga S., Halaçlι S., Aytekin E., Yaz İ., et al.

Asian Pacific journal of allergy and immunology , 2019 (SCI-Expanded)

ADA2 deficiency in a patient with Noonan syndrome-like disorder with loose anagen hair: The co-occurrence of two rare syndromes

Akgun-Dogan O., Simsek-Kiper P. O., Taskiran E., Lissewski C., Brinkmann J., Schanze D., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.179, no.12, pp.2474-2480, 2019 (SCI-Expanded)

A Spectrum of Clinical Findings from ALPS to CVID: Several Novel LRBA Defects.

Cagdas D. N., Halaçlı S., Tan Ç., Lo B., Çetinkaya P., Esenboğa S., et al.

Journal of clinical immunology , vol.39, no.7, pp.726-738, 2019 (SCI-Expanded) Sustainable Development

Bone marrow transplantation with Favorable outcome in three patients with LPS-responsive beige like anchor (LRBA) deficiency

OKUR F. V., KUŞKONMAZ B. B., Cagdas D. N., Tezcan I., Uckan-Cetinkaya D.

CLINICAL IMMUNOLOGY , vol.203, pp.162-165, 2019 (SCI-Expanded)

Clinical Features and HSCT Outcome for SCID in Turkey

Ikinciogullari A., Cagdas D. N., Dogu F., Tugrul T., Karasu G., Haskologlu S., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , vol.39, no.3, pp.316-323, 2019 (SCI-Expanded)

Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function

Shahin T., Aschenbrenner D., Cagdas D., Bal S. K., Conde C. D., Garncarz W., et al.

HAEMATOLOGICA , vol.104, no.3, pp.609-621, 2019 (SCI-Expanded)

Tumor necrosis factor alpha-308 G/A and interleukin 1 beta-511 C/T gene polymorphisms in patients with scarring acne

Akoglu G., TAN Ç., Ayvaz D. N., Tezcan I.

JOURNAL OF COSMETIC DERMATOLOGY , vol.18, no.1, pp.395-400, 2019 (SCI-Expanded)

Two siblings with PRKDC defect who presented with cutaneous granulomas and review of the literature

Esenboga S., AKAL C., Karaatmaca B., Erman B., Dogan S., ORHAN D., et al.

CLINICAL IMMUNOLOGY , vol.197, pp.1-5, 2018 (SCI-Expanded)

B lymphocyte subsets and outcomes in patients with an initial diagnosis of transient hypogammaglobulinemia of infancy

Eroglu F. K., Kaya F. S. F., Cagdas D. N., Ozgur T. T., Yılmaz T., Tezcan I., et al.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY , vol.88, no.4, 2018 (SCI-Expanded)

Type I IFN-related NETosis in ataxia telangiectasia and Artemis deficiency

Gul E., Sayar E. H., Gungor B., Eroglu F. K., Surucu N., Keles S., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , vol.142, no.1, pp.246-257, 2018 (SCI-Expanded)

A young girl with severe cerebral fungal infection due to card 9 deficiency

Cetinkaya P. G., Ayvaz D. N., KARAATMACA B., GÖÇMEN R., Soylemezoglu F., Bainter W., et al.

CLINICAL IMMUNOLOGY , vol.191, pp.21-26, 2018 (SCI-Expanded)

ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome

CAGDAS D., CETINKAYA P. G., KARAATMACA B., Esenboga S., TAN Ç., YILMAZ T., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , vol.38, no.4, pp.484-493, 2018 (SCI-Expanded)

Advantage of the subcutaneous immunoglobulin replacement therapy in primary immunodeficient patients with or without secondary protein loss

Gur-Cetinkaya P., Cagdas-Ayvaz D. N., Oksuz A. B., Ertoy A., Hayran U., Ozkan F., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.60, no.3, pp.270-276, 2018 (SCI-Expanded)

Neurologic Involvement in Primary Immunodeficiency Disorders

Yildirim M., Ayvaz D. N., Konuskan B., GÖÇMEN R., Tezcan I., TOPÇU M., et al.

JOURNAL OF CHILD NEUROLOGY , vol.33, no.5, pp.320-328, 2018 (SCI-Expanded)

A Rare Cause of Secondary Immunodeficiency: Generalized Lymphatic Anomaly

Esenboga S., Cagdas D. N., OĞUZ B., Bajin I., AYDIN G. B., Akyuz C., et al.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , vol.40, no.3, pp.248-251, 2018 (SCI-Expanded)

Clinical and genetic features of the patients with X-Linked agammaglobulinemia from Turkey: Single-centre experience

Esenboga S., Cagdas D. N., Ozgur T. T., Cetinkaya P. G., Turkdemir L. M., Sanal O., et al.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY , vol.87, no.3, 2018 (SCI-Expanded)

Successful hematopoietic stem cell transplantation after myeloablative conditioning in three patients with dedicator of cytokinesis 8 deficiency (DOCK8) related Hyper IgE syndrome

Kuskonmaz B. B., Ayvaz D. N., Tezcan I., YÜCE A., Sanal O., ÇETİNKAYA F. D.

BONE MARROW TRANSPLANTATION , vol.53, no.3, pp.339-343, 2018 (SCI-Expanded)

Hypomorphic RAG1 defect in a child presented with pulmonary hemorrhage and digital necrosis

Taşkıran E., Sönmez H., Ayvaz D. N., Koşukcu C., Batu E. D., Esenboğa S., et al.

CLINICAL IMMUNOLOGY , vol.187, pp.92-94, 2018 (SCI-Expanded)

A Novel Homozygous Mutation With Different Clinical Presentations in 2 IRAK-4-Deficient Siblings: First Case With Recurrent Salmonellosis and Non-Hodgkin Lymphoma

Gokturk B., Casanova J. L., Picard C., Ayvaz C. D., ERMAN B., Tezcan I., et al.

JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY , vol.28, no.4, pp.271-273, 2018 (SCI-Expanded)

The 44th Annual Meeting of the European Society for Blood and Marrow Transplantation: Physicians Poster Sessions

ÇAĞDAŞ AYVAZ D. N., GÜR ÇETİNKAYA P., KARAATMACA b., ESENBOĞA S., TAN Ç., YILMAZ T., et al.

Bone Marrow Transplantation , 2018 (SCI-Expanded)

Acute myeloid leukemia in a child with dedicator of cytokinesis 8 (DOCK8) deficiency

Kuşkonmaz B. B., Ayvaz D. N., Barış S., Ünal Ş., Tezcan İ., Uçkan D.

PEDIATRIC BLOOD & CANCER , vol.64, no.12, 2017 (SCI-Expanded)

Hematopoietic stem cell transplantation in children with Griscelli syndrome: A single-center experience

Kuskonmaz B. B., ÇAĞDAŞ AYVAZ D. N., Gokce M., Ozgur T. T., OKUR F. V., Cetin M., et al.

PEDIATRIC TRANSPLANTATION , vol.21, no.7, 2017 (SCI-Expanded)

Progressive multifocal leukoencephalopathy in a patient with lymphoma and presumptive hyper IgE syndrome

GÖÇMEN R., Acar N. P., Cagdas D. N., Kurne A.

Journal of NeuroVirology , vol.23, no.4, pp.632-636, 2017 (SCI-Expanded)

A novel mutation in TAP1 gene leading to MHC class I deficiency: Report of two cases and review of the literature

HANALİOĞLU D., ÇAĞDAŞ AYVAZ D. N., Ozgur T. T., van der Burg M., Sanal O., Tezcan I.

CLINICAL IMMUNOLOGY , vol.178, pp.74-78, 2017 (SCI-Expanded) Sustainable Development

Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD

Esenboga S., EMİRALİOĞLU N., Cagdas D. N., Erman B., De Boer M., OĞUZ B., et al.

Journal of Clinical Immunology , vol.37, no.3, pp.269-272, 2017 (SCI-Expanded)

Investigation of Genetic Defects in Severe Combined Immunodeficiency Patients from Turkey by Targeted Sequencing

ERMAN B., Bilic I., Hirschmugl T., Salzer E., Boztug H., Sanal O., et al.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY , vol.85, no.3, pp.227-234, 2017 (SCI-Expanded)

Course of IL-2-inducible T-cell kinase deficiency in a family: lymphomatoid granulomatosis, lymphoma and allogeneic bone marrow transplantation in one sibling; and death in the other

ÇAĞDAŞ AYVAZ D. N., ERMAN B., Hanoglu D., Tavil B., KUŞKONMAZ B. B., AYDIN G. B., et al.

BONE MARROW TRANSPLANTATION , vol.52, no.1, pp.126-129, 2017 (SCI-Expanded)

Low T Cell Numbers Resembling T-B plus SCID in a Patient with Wiskott-Aldrich Syndrome and the Outcome of Two Hematopoietic Stem Cell Transplantations

ÇAĞDAŞ AYVAZ D. N., Aytac Ş. S., Kuskonmaz B. B., Ariga T., van der Burg M., ÇETİNKAYA F. D., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , vol.37, no.1, pp.18-21, 2017 (SCI-Expanded)

Defective pneumococcal antibody response in patients with recurrent respiratory tract infections.

Erman B., Demirtaş D., Bildik H., Çağdaş-Ayvaz D. N., Sanal Ö., Tezcan İ.

The Turkish journal of pediatrics , vol.59, no.5, pp.555-560, 2017 (SCI-Expanded)

RASGRP1 deficiency causes immunodeficiency with impaired cytoskeletal dynamics

Salzer E., ÇAĞDAŞ AYVAZ D. N., Hons M., Mace E. M., Garncarz W., Petronczki O. Y., et al.

NATURE IMMUNOLOGY , vol.17, no.12, pp.1352-1360, 2016 (SCI-Expanded)

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

Toubiana J., Okada S., Hiller J., Oleastro M., Lagos Gomez M., Aldave Becerra J. C., et al.

BLOOD , vol.127, no.25, pp.3154-3164, 2016 (SCI-Expanded)

Detection of parasites in children with chronic diarrhea

Macin S., Kaya F., Cagdas D. N., HIZARCIOGLU-GULSEN H., Saltik-Temizel I. N., Tezcan I., et al.

Pediatrics International , vol.58, no.6, pp.531-533, 2016 (SCI-Expanded) Sustainable Development

Successful outcome with second hematopoietic stem cell transplantation in a patient with IL-10R deficiency

KUŞKONMAZ B. B., Ayvaz D. N., Aydemir Y., Erman B., Tavil B., ÖZEN H., et al.

BONE MARROW TRANSPLANTATION , vol.51, no.4, pp.615-616, 2016 (SCI-Expanded)

Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal association

Yee C., Massaad M., Bainter W., Ohsumi T., Föger N., Chan A., et al.

Journal of Allergy and Clinical Immunology , vol.137, no.3, pp.879, 2016 (SCI-Expanded)

An infant with ZAP-70 deficiency with disseminated mycobacterial disease

Esenboga S., ÇAĞDAŞ AYVAZ D. N., Cetinkaya P. G., van der Burg M., Tezcan I.

JOURNAL OF CLINICAL IMMUNOLOGY , vol.36, no.2, pp.103-106, 2016 (SCI-Expanded)

Clinical and genetic features of IL12Rβ1 deficiency: Single center experience of 18 patients

TAN Ç., Cagdas-Ayvaz D. N., Metin A., Keskin O., Tezcan I., Sanal O.

Turkish Journal of Pediatrics , vol.58, no.4, pp.356-361, 2016 (SCI-Expanded)

Pediatric-onset adult type sarcoidosis: A case report

ÖZSÜREKCİ Y., CENGİZ A. B., DÜZOVA A., SAĞ E., KADAYIFÇILAR S., ERSOZ D., et al.

ARCHIVOS ARGENTINOS DE PEDIATRIA , vol.113, no.6, 2015 (SCI-Expanded)

STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation

HALACLI S. O., AYVAZ D. N., Sun-Tan C., Erman B., Uz E., YILMAZ D. Y., et al.

CLINICAL IMMUNOLOGY , vol.161, no.2, pp.316-323, 2015 (SCI-Expanded)

Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R.

Erman B., Bilic I., Hirschmugl T., Salzer E., ÇAĞDAŞ AYVAZ D. N., Esenboga S., et al.

Haematologica , vol.100, no.6, 2015 (SCI-Expanded)

Polymorphisms in FAS and CASP8 genes may contribute to the development of ALPS phenotype: A study in 25 patients with probable ALPS

TAN Ç., ÖZGÜL R. K., CAGDAS-AYVAZ D. N., TEZCAN I., SANAL O.

Turkish Journal of Pediatrics , vol.57, no.2, pp.141-145, 2015 (SCI-Expanded)

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients

Aydin S. E., Kilic S. S., Aytekin C., Kumar A., Porras O., Kainulainen L., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , vol.35, no.2, pp.189-198, 2015 (SCI-Expanded) Sustainable Development

Diagnosis: Melanoderma after Hematopoietic Stem Cell Transplantation

ÜNAL Ş., Tezcan I., Gucer S., Boyraz M. S., Cagdas D. N., Cetinkaya D. U.

TURKISH JOURNAL OF HEMATOLOGY , vol.32, no.4, pp.378-379, 2015 (SCI-Expanded)

Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion

YILMAZ M., ÇAĞDAŞ AYVAZ D. N., Grandin V., ALTINTAŞ D. U., Tezcan I., de Saint Basile G., et al.

PEDIATRIC ALLERGY AND IMMUNOLOGY , vol.25, no.8, pp.817-819, 2014 (SCI-Expanded)

A Novel Mutation in Leukocyte Adhesion Deficiency Type II/CDGIIc

ÇAĞDAŞ AYVAZ D. N., YILMAZ M., KANDEMİR N., Tezcan I., Etzioni A., Sanal O.

JOURNAL OF CLINICAL IMMUNOLOGY , vol.34, no.8, pp.1009-1014, 2014 (SCI-Expanded) Sustainable Development

Identification of ITK deficiency as a novel genetic cause of idiopathic CD4(+) T-cell lymphopenia

Serwas N. K., ÇAĞDAŞ AYVAZ D. N., Ban S. A., Bienemann K., Salzer E., Tezcan I., et al.

BLOOD , vol.124, no.4, pp.655-657, 2014 (SCI-Expanded)

Successful Treatment of Severe Myasthenia Gravis Developed After Allogeneic Hematopoietic Stem Cell Transplantation With Plasma Exchange and Rituximab

ÜNAL Ş., SAĞ E., KUSKONMAZ B. B., Kesici S., BAYRAKCİ B., AYVAZ D. N., et al.

PEDIATRIC BLOOD & CANCER , vol.61, no.5, pp.928-930, 2014 (SCI-Expanded)

Metamizole-Induced Bicytopenia Reversed by G-CSF and IVIG Treatment in a Child

Tavil B., Cetin M., Gumruk F., ÇAĞDAŞ AYVAZ D. N., CENGİZ A. B.

PEDIATRIC HEMATOLOGY AND ONCOLOGY , vol.31, no.2, pp.117-119, 2014 (SCI-Expanded)

Progressive neurodegenerative syndrome in a patient with x-linked agammaglobulinemia receiving intravenous immunoglobulin therapy

Sag A., SAKA E., Ozgur T. T., SANAL O., AYVAZ D. N., ELİBOL B., et al.

Cognitive and Behavioral Neurology , vol.27, no.3, pp.155-159, 2014 (SCI-Expanded)

Atypical combined immunodeficiency due to Artemis defect: a case presenting as hyperimmunoglobulin M syndrome and with LGLL.

Bajin İ., Ayvaz D. N., Ünal Ş., Özgür T., Çetin M., Gümrük F., et al.

Molecular immunology , vol.56, no.4, pp.354-7, 2013 (SCI-Expanded)

IL-12R beta 1 Deficiency: Mutation Update and Description of the IL12RB1 Variation Database

VAN DE VOSSE E., HAVERKAMP M. H., RAMIREZ-ALEJO N., MARTINEZ-GALLO M., BLANCAS-GALICIA L., METIN A., et al.

HUMAN MUTATION , vol.34, no.10, pp.1329-1339, 2013 (SCI-Expanded)

Diet and physical activity interventions do have effects on body composition and metabolic syndrome parameters in overweight and obese adolescents and their mothers

Nişanci-Kilinç F., Çaǧdaş D. N.

Turkish Journal of Pediatrics , vol.55, no.3, pp.292-299, 2013 (SCI-Expanded) Sustainable Development

A Case of DOCK8 Deficient Hyper-IgE Syndrome Presenting Primarily With Eczema, Food Allergy, and Asthma

Cavkaytar O., ÇAĞDAŞ AYVAZ D. N., Keskin O., Yilmaz E. A., Buyuktiryaki B., ŞAHİNER Ü. M., et al.

PEDIATRIC ALLERGY IMMUNOLOGY AND PULMONOLOGY , vol.26, no.1, pp.48-51, 2013 (SCI-Expanded) Sustainable Development

Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients

ÇAĞDAŞ AYVAZ D. N., Ozgur T. T., Asal G. T., Tezcan I., Metin A., Lambert N., et al.

EUROPEAN JOURNAL OF PEDIATRICS , vol.171, no.10, pp.1527-1531, 2012 (SCI-Expanded)

Evaluation of body compositions, dietary habits and nutritional knowledge of health college students

Kilinc F. N., ÇAĞDAŞ AYVAZ D. N.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.47, no.3, pp.181-188, 2012 (SCI-Expanded)

Additional Diverse Findings Expand the Clinical Presentation of DOCK8 Deficiency

Sanal O., Jing H., Ozgur T., Ayvaz D. N., Strauss-Albee D. M., Ersoy-Evans S., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , vol.32, no.4, pp.698-708, 2012 (SCI-Expanded)

Two SCID cases with Cernunnos-XLF deficiency successfully treated by hematopoietic stem cell transplantation

ÇAĞDAŞ AYVAZ D. N., Ozgur T. T., Asal G. T., Revy P., De Villartay J., van der Burg M., et al.

PEDIATRIC TRANSPLANTATION , vol.16, no.5, 2012 (SCI-Expanded) Sustainable Development

Chronic granulomatous disease presenting with hypogammaglobulinemia

Hanoglu D., OZGUR T. T., Ayvaz D. N., KOKER M. Y., Sanal O.

Journal of Investigational Allergology and Clinical Immunology , vol.21, no.4, pp.310-312, 2011 (SCI-Expanded)

Anthropometric measurements and body composition analysis of obese adolescents with and without metabolic syndrome

Ayvaz D. N., Kilinc F. N., Pac F. A., Cakal E.

TURKISH JOURNAL OF MEDICAL SCIENCES , vol.41, no.2, pp.267-274, 2011 (SCI-Expanded)

Author's reply

ÇAĞDAŞ AYVAZ D. N.

Anadolu Kardiyoloji Dergisi , vol.10, no.4, pp.383, 2010 (SCI-Expanded)

Kounis syndrome: A forgotten cause of chest pain/Cardiac chest pain in children Reply

Ayvaz D. N.

ANATOLIAN JOURNAL OF CARDIOLOGY , vol.10, no.4, pp.382-383, 2010 (SCI-Expanded)

Hepatopulmonary syndrome associated with budd-chiari syndrome Budd-Chiari sendromu ile birliktelik gösteren hepatopulmoner sendrom

Paç F. A., Çaǧdaş D. N., Akdoǧan M., Zengin N. I., Şaşmaz N.

Anadolu Kardiyoloji Dergisi , vol.10, no.3, pp.286-288, 2010 (SCI-Expanded)

Cardiac chest pain in children

Çaǧdaş D. N., Paç F. A.

Anadolu Kardiyoloji Dergisi , vol.9, no.5, pp.401-406, 2009 (SCI-Expanded)

A case of cardiac valvular dysplasia

Çaǧdaş D. N., Ayşenur Paç F.

Anadolu Kardiyoloji Dergisi , vol.9, no.6, 2009 (SCI-Expanded)

Ventricular septal diverticule and ventricular septal defect after penetrating cardiac trauma

Paç F. A., Çaǧdaş D. N.

Anadolu Kardiyoloji Dergisi , vol.9, no.1, pp.62-63, 2009 (SCI-Expanded)

Glucocorticoid-induced Diabetic Ketoacidosis in Acute Rheumatic Fever

Cagdas D. N., Pac F. A., Cakal E.

JOURNAL OF CARDIOVASCULAR PHARMACOLOGY AND THERAPEUTICS , vol.13, no.4, pp.298-300, 2008 (SCI-Expanded) Sustainable Development

A Turkish family with Ellis-van Creveld syndrome in six siblings; linkage analysis on 4p16 region (D4S3360-D4S2366)

Çaǧdaş D. N., Parlar A., Pac A., Tutun U., Pac M., Balci A. S.

Genetic Counseling , vol.19, no.4, pp.387-395, 2008 (SCI-Expanded)

Premature ventricular contractions in normal children

ÇAĞDAŞ AYVAZ D. N., Çeliker A., Özer S.

Turkish Journal of Pediatrics , vol.50, no.3, pp.260-264, 2008 (SCI-Expanded)

Axenfeld-Rieger syndrome and pseudotruncus arteriosus

Pac F. A., Cagdas D. N., Demir M. N.

INTERNATIONAL JOURNAL OF CARDIOLOGY , vol.126, no.1, 2008 (SCI-Expanded)

Congenital left ventricular apical diverticulum

Pac F. A., Cagdas D. N.

ANADOLU KARDIYOLOJI DERGISI-THE ANATOLIAN JOURNAL OF CARDIOLOGY , vol.8, no.1, pp.91, 2008 (SCI-Expanded)

Community-acquired pneumonia and parapneumonic effusions in developing countries

Seçmeer G., ÇİFTÇİ A. Ö., Kanra G., CEYHAN M., KARA A., CENGİZ A. B., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.50, no.1, pp.51-57, 2008 (SCI-Expanded)

Treatment of massive cardiac thrombi in a patient with protein C and protein S deficiency

Pac F. A., Cagdas D. N.

BLOOD COAGULATION & FIBRINOLYSIS , vol.18, no.7, pp.699-702, 2007 (SCI-Expanded)

Left main coronary artery and aortic root compression associated with atrial septal defect and pulmonary hypertension

Paç F. A., Çaǧdaş D. N., Ulaş M., Özatik M. A., Paç M.

International Journal of Cardiology , vol.118, no.2, 2007 (SCI-Expanded)

Familial Mediterranean fever and mesangial proliferative glomerulonephritis: Report of a case and review of the literature

Cagdas D. N., Gucer S., Kale G., Duzova A., Ozen S.

Pediatric Nephrology , vol.20, no.9, pp.1352-1354, 2005 (SCI-Expanded)

Right-sided Duane retraction syndrome associated with multiple malformations

Yalcin S. S., Cagdas D. N., Sener E., Yurdakok K.

Pediatrics International , vol.45, no.5, pp.577-579, 2003 (SCI-Expanded)

Articles Published in Other Journals

Is Cauda Equina Involvement Related to BK Virus in Patients with Combined Immunodeficiency?

Sonmez G., Kalaycı F. N. C., Gocmen R., Ozsurekcı Y., Çağdaş Ayvaz D. N.

INDIAN JOURNAL OF RADIOLOGY AND IMAGING , vol.1, no.1, pp.1-3, 2025 (ESCI) Sustainable Development

An Adult-Onset Chronic Granulomatous Disease Case with Hemophagocytic Lymphohistiocytosis Caused by Burkholderia and Aspergillus Infections.

Kaygusuz Y., Üstün C., Er A. G., Kiki Z., Yaz İ., Tüten-Dal S., et al.

Infectious diseases & clinical microbiology , vol.6, no.4, pp.334-338, 2024 (Peer-Reviewed Journal)

Griscelli syndrome: Erdheim-Chester disease-like local presentation progressing to accelerated phase

Solakoğlu T., Sönmez G., Tenekeci A. K., Altunbüker H., Akar H. T., Tezcan F. İ., et al.

The Turkish Journal of Pediatrics , vol.1, no.1, pp.1-5, 2024 (Peer-Reviewed Journal) Sustainable Development

False Negative Next-Generation-Sequencing Analysis in a Lipopolysa ccharide-Responsive Beige-Like Anchor Defect.

Ünal T., Esenboğa S., Oskay Halaçlı S., Tezcan I., Çağdaş D. N.

Turkish archives of pediatrics , vol.59, no.2, pp.221-223, 2024 (ESCI) Sustainable Development

Psychosocial Functionality in Adolescents with Inborn Errors of Immunity During the COVID-19 Pandemic

Güven A. G., Esenboğa S., Kızılkan M. P., Aslan C., Akarsu A., Karabulut E., et al.

Turkish Journal of Pediatric Disease , vol.1, no.1, pp.1-2, 2024 (Peer-Reviewed Journal)

A Novel Interleukin 17 Receptor A Mutation in a Child with Chronic Mucocutaneous Candidiasis and Staphylococcal Skin Infections

Yakici N., , Oskay Halacli S., Tan C., Gur Cetinkaya P., Akar H. T., et al.

TURK PEDIATRI ARSIVI , vol.1, no.1, pp.1-3, 2023 (Scopus) Sustainable Development

Liver immunity, autoimmunity, and inborn errors of immunity

PARLAR Y. E., AYAR Ş. N., ÇAĞDAŞ AYVAZ D. N., BALABAN H. Y.

World Journal of Hepatology , vol.15, no.1, pp.52-67, 2023 (ESCI)

Hyper IgM Syndrome with a Novel Mutation in the AICDA Gene: Easy to Diagnose

ÖZDEMİRAL C., ESENBOĞA S., BİLDİK H. N., ÇAĞDAŞ AYVAZ D. N., Tezcan I.

Asthma Allergy Immunology , vol.21, no.1, pp.64-67, 2023 (Scopus)

A Patient Presenting with Chronic Mucocutaneous Candidiasis: A Novel IL12RB1 Mutation

ESENBOĞA S., BİLDİK H. N., OCAK M., ÇAĞDAŞ AYVAZ D. N., TEZCAN F. İ.

ASTIM ALLERJI IMMUNOLOJI , vol.20, pp.194-196, 2022 (ESCI)

Mutation in BTK Gene Causing an Atypical Presentation of XLA

Esenboğa S., Ucler H., Oskay Halaclı S., Tan C., Kendırcı N., Zhang Y., et al.

ASTIM ALLERJI IMMUNOLOJI , vol.20, no.3, pp.197-201, 2022 (Scopus) Sustainable Development

Evaluation of Health Status and Quality of Life in Patients Using Intravenous and Subcutaneous Forms of Immunoglobulin Replacement İntravenöz ve Subkütan İmmünoglobulin Replasman Tedavisi Kullanan Hastalarda Sağlık Durumu ve Yaşam Kalitesinin Değerlendirilmesi

ESENBOĞA S., AKARSU A., BİLDİK H. N., ÇAĞDAŞ AYVAZ D. N., TEZCAN F. İ.

Ankara Üniversitesi Tıp Fakültesi Mecmuası , vol.75, no.1, pp.77-83, 2022 (Peer-Reviewed Journal)

Evaluation of Health Status and Quality of Life in Patients Using Intravenous and Subcutaneous Forms of Immunoglobulin Replacement

Esenboğa S., Akarsu A., Bildik H. N., Çağdaş Ayvaz D. N., Tezcan İ.

Ankara Üniversitesi Tıp Fakültesi Mecmuası , vol.75, no.1, pp.77-83, 2022 (Peer-Reviewed Journal)

Awareness Concerning Primary Immunodeficiencies Among Physicians in Turkey

ESENBOĞA S., BİLDİK H. N., OCAK M., Aytekin E. S. O. Y. A. K., ÇAĞDAŞ AYVAZ D. N., TEZCAN F. İ.

ASTIM ALLERJI IMMUNOLOJI , vol.20, no.1, pp.55-63, 2022 (ESCI)

Evaluation of the peripheral blood T and B cell subsets and IRF-7 variants in adult patients with severe influenza virus infection

Basaran N. C., TAN Ç., ÖZIŞIK L., ÖZBEK B., İNKAYA A. Ç., ÖZYAVUZ ALP Ş., et al.

HEALTH SCIENCE REPORTS , vol.5, no.1, 2022 (ESCI)

Uzamış bakteriyel bronşit tanısı alan hastalarda immunolojik değerlendirme yapılmalı mıdır?

ÇAĞDAŞ AYVAZ D. N., TEZCAN F. İ., KİPER E. N., GÜZELKAŞ İ., EMİRALİOĞLU N., YALÇIN E. E., et al.

COCUK SAGLIGI VE HASTALIKLARI DERGISI , vol.65, no.1, pp.14-18, 2022 (Scopus)

DiGeorge Syndrome: Simultaneously Diagnosis of A Mother-Baby Pair With Great Clinical Variability

Dokuzboy R. S., Sari F. N., Beser E., ÇAĞDAŞ AYVAZ D. N., Dizdar E. A.

GAZI MEDICAL JOURNAL , vol.33, no.2, pp.179-182, 2022 (ESCI)

Should immunological evaluation be performed in patients diagnosed with protracted bacterial bronchitis? Uzamış bakteriyel bronşit tanısı alan hastalarda immunolojik değerlendirme yapılmalı mıdır?

GÜZELKAŞ İ., EMİRALİOĞLU ORDUKAYA N., Yalçın E., DOĞRU ERSÖZ D., ÇAĞDAŞ AYVAZ D. N., Tezcan İ., et al.

Cocuk Sagligi ve Hastaliklari Dergisi , vol.65, no.1, pp.14-18, 2022 (Scopus)

Characteristics of patients with C1 esterase inhibitor deficiency: a single center study.

Aytekin E., Cagdas D. N., Tan C., Tezcan I.

European annals of allergy and clinical immunology , vol.53, pp.75-79, 2021 (ESCI)

Flow Cytometric Analysis of T Cell V beta Repertoire in Common Variable Immunodeficiency Patients with TACI Mutations

OSKAY HALAÇLI S., ÖZBEK B., Aytekin E. S., YAZ İ., TAN Ç., ÇAĞDAŞ AYVAZ D. N., et al.

TURKISH JOURNAL OF IMMUNOLOGY , vol.9, no.1, pp.12-19, 2021 (ESCI)

Flow Cytometric Analysis of T Cell Vβ Repertoire in Common Variable Immunodeficiency Patients with TACI Mutations

OSKAY HALAÇLI S., ÖZBEK B., SOYAK AYTEKİN E., YAZ İ., TAN Ç., ÇAĞDAŞ AYVAZ D. N., et al.

TURKISH JOURNAL OF IMMUNOLOGY , vol.9, no.1, pp.12-19, 2021 (ESCI)

Primary immunodeficiency disorders in children with Non-Cystic Fibrosis Bronchiectasis.

Cagdas D. N., Pehlivanturk K., Tagiyev A., Emiralioglu N., Keleþ A., Yalcyn E., et al.

European annals of allergy and clinical immunology , vol.52, pp.271-276, 2020 (ESCI)

Flow Cytometry is a Reliable Tool in the Diagnosis of STK4 Deficiency

Oskay Halaçlı S., Çağdaş Ayvaz D. N., Tezcan F. İ.

ASTIM ALLERJI IMMUNOLOJI , vol.18, pp.113-117, 2020 (ESCI)

Retroperitoneal Abscess in Severe Combined Immunodeficiency Probably Due to BCG Vaccine

Gur Cetinkaya P., Cagdas D. N., Ozcelik U., Tezcan I.

ASTIM ALLERJI IMMUNOLOJI , vol.18, no.2, pp.98-101, 2020 (ESCI) Sustainable Development

The significance of Western Blot in Primary Immunodeficiencies: Examples from two families

Halacli S., Cagdas D. N., TEZCAN F. İ.

TURKISH JOURNAL OF IMMUNOLOGY , vol.7, no.3, pp.120-124, 2019 (ESCI)

Axillary Lymphadenopathy: Only Presentation in an Infant Diagnosed with Chronic Granulomatous Disease

GÜR ÇETİNKAYA P., ÇAĞDAŞ AYVAZ D. N., TEZCAN F. İ.

Kafkas Journal of Medical Sciences , vol.9, 2019 (Peer-Reviewed Journal)

The Association Between Vitamin D Levels and Infections in Patients with Primary Immunodeficiency

Gur Cetinkaya P., ÇAĞDAŞ AYVAZ D. N., Cuzdanci H., Tezcan I.

TURKISH JOURNAL OF IMMUNOLOGY , vol.7, no.2, pp.83-92, 2019 (ESCI)

Besin Alerjisi: Türk Ulusal Rehberi 2017

ALTINTAŞ D. U., BÜYÜKTİRYAKİ A. B., ÇAĞDAŞ AYVAZ D. N., BABAYİĞİT HOCAOĞLU A., BİNGÖL G., BİNGÖL A., et al.

Astım Allerji İmmünoloji , vol.15, 2017 (Peer-Reviewed Journal)

Besin allerjisi: Türk Ulusal Rehber 2017 (Besin katkı maddeleri allerjisi)

ALTINTAŞ D. U., BÜYÜKTİRYAKİ A. B., ÇAĞDAŞ AYVAZ D. N., BABAYİĞİT HOCAOĞLU A., BİNGÖL A., BİNGÖL G., et al.

Astım Allerji İmmunoloji , vol.15, 2017 (Peer-Reviewed Journal)

An Adult Patient with Monosomy 18p Growth Hormone Deficiency and Selective IgA Deficiency

ZENGİN AKKUŞ P., çetinkaya a., ÇAĞDAŞ AYVAZ D. N., ALİKAŞİFOĞLU M., ALİKAŞİFOĞLU A., KANDEMİR N., et al.

Journal of Genetic Syndromes & Gene Therapy , vol.7, no.2, 2016 (Peer-Reviewed Journal)

65 Year Old Patient with Common Variable Immunodeficiency: 3 Years Followup and Development of Lung Adeno Carcinoma, is it a Coincidence?

Çağdaş Ayvaz D. N.

Journal of Pulmonary & Respiratory Medicine , vol.5, no.4, pp.277-279, 2015 (Peer-Reviewed Journal)

CVID Associated with Systemic Amyloidosis

Esenboga S., ÇAĞDAŞ AYVAZ D. N., Ayhan A. S., PEYNİRCİOĞLU B., Sanal O., Tezcan I.

CASE REPORTS IN IMMUNOLOGY , 2015 (ESCI)

Politik İstikrarsızlık ve Yolsuzluk İlişkisi Bir Panel Veri Analizi

ERKAL G., AKINCI M., YILMAZ Ö., ÇAĞDAŞ AYVAZ D. N., ESENBOĞA S.

EGE ACADEMIC REVIEW , vol.15, no.3, pp.327-342, 2015 (Peer-Reviewed Journal)

The Role of IL 12Rß1 Expression Analysis Using Flow Cytometry in the Diagnosis of IL 12Rß1 Deficiency

TAN Ç., ÇAĞDAŞ AYVAZ D. N., TEZCAN F. İ., SANAL Ö.

Turkish Journal of Immunology , vol.1, pp.1-4, 2013 (Scopus)

The Role of IL-12R beta 1 Expression Analysis Using Flow Cytometry in the Diagnosis of IL-12R beta 1 Deficiency

Tan C. S., Ayvaz D. N., Tezcan I., Sanal O.

TURKISH JOURNAL OF IMMUNOLOGY , vol.1, no.1, pp.1-4, 2013 (Scopus)

Apoptosis in Autoimmune Lymphoproliferative Syndrome Suspected Patients with Clinical and Laboratory Findings

ERMAN B., ÇAĞDAŞ AYVAZ D. N., Metin A., Tezcan I., Sanal O.

TURKISH JOURNAL OF IMMUNOLOGY , vol.1, no.1, pp.5-12, 2013 (ESCI)

Klinik ve Laboratuvar Özellikleri ile Otoimmün Lenfoproliferatif Sendrom Düşünülen Hastalarda Apoptoz

ERMAN B., ÇAĞDAŞ AYVAZ D. N., Metin A., TEZCAN F. İ., SANAL Ş. Ö.

TURKISH JOURNAL OF IMMUNOLOGY , vol.1, no.1, pp.5-12, 2013 (Scopus)

Glycogen storage disease and hemophagocytosis: A case report Glikojen depo hastaliǧi ve hemofagositik lenfohistiyositoz birlikteliǧi: Bir vaka takdimi

Çaǧdaš D. N., YURDAKÖK M., COŞKUN T., DEMİR H.

Cocuk Sagligi ve Hastaliklari Dergisi , vol.53, no.3, pp.216-219, 2010 (Scopus)

Glikojen depo hastalığı ve hemofagositik lenfohistiyositoz birlikteliği:Bir vaka takdimi

Çağdaş Ayvaz D. N., Yurdakök M., Coşkun T., Demir H.

Çocuk Sağlığı ve Hastalıkları Dergisi , no.53, pp.216-219, 2010 (Scopus)

Zayıflama diyetlerinde kullanılan balık yağının biyokimyasal parametreler üzerine etkisi

NİŞANCI KILINÇ F., DEMİRBAĞ A., ÇAĞDAŞ AYVAZ D. N., TEMİZHAN A., BESLER H. T.

MN Kardiyoloji , vol.16, no.4, pp.239-246, 2009 (Peer-Reviewed Journal)

Papers Presented at Peer-Reviewed Scientific Conferences

Hafif/orta ve ağır erişkin COVID-19 hastalarının immün fenotiplerinin belirlenmesi ve genetik yatkınlık varlığının araştırılması

ÇALIK BAŞARAN N., TAN Ç., ÖZDEDE M., UYAROĞLU O. A., HALAÇLI B., DEĞİRMENCİLER R. F., et al.

9.KLİNİK İMMÜNOLOJİ KONGRESİ, Antalya, Turkey, 01 May 2023, (Summary Text)

Good Sendromu: Olgu Sunumu

KAZANCIOĞLU A., CAKA C., ALİYEVA G., ÜSTÜN C., SOYAK AYTEKİN E., ESENBOĞA S., et al.

XXX. ULUSLARARASI KATILIMLI ULUSAL ALLERJİ KLİNİK İMMÜNOLOJİ KONGRESİ, Turkey, 27 November - 01 December 2024, (Summary Text)

Büyüme Gelişme Geriliği, Kraniofasiyal Dismorfizm ve Kombine İmmün Yetmezlik ile Seyreden Bir Olgu: KMT2C Mutasyonu

FATHELBAB J., DEMİRSU A., YAZ İ., KAZANCIOĞLU A., SOYAK AYTEKİN E., ESENBOĞA S., et al.

XXX. ULUSLARARASI KATILIMLI ULUSAL ALLERJİ KLİNİK İMMÜNOLOJİ KONGRESİ, Turkey, 27 November 2024, (Summary Text)

HOW EARLY DIAGNOSIS CAN BE IMPROVED IN PRIMARY IMMUNODEFICIENCY (PID): THE FIRST ITALIANTURKISH JOINT WORKSHOP

İKİNCİOĞULLARI K. A., DOĞU E. F., Guarnieri V., HASKOLOĞLU Z. Ş., Allegrini C., İSLAMOĞLU C., et al.

21th Biennial Meeting of ESID, Marseille, France, 15 - 18 October 2024, (Full Text)

Inflammatory parameters and innate lymphoid cells in chilhood interstitial lung diseases: a prospective study

Hizal M., Oskay Halaçlı S., Nayır-Büyükşahin H, H., Çiftçier B., Yılmaz K., Emiralioglu Ordukaya N., et al.

ERS Congress 2024 abstracts, 14 September 2024, pp.1, (Full Text)

ERİŞKİN İMMÜNYETMEZLİKLİ HASTALARDA SAĞLIKLA İLİŞKİLİ YAŞAM KALİTESİ VE ÇALIŞMA DURUMLARININ BELİRLENMESİ

MADEN S., ÖZDEDE M., ÖZDEMİRAL C., ESENBOĞA S., SÖNMEZER M. Ç., İNKAYA A. Ç., et al.

25. ULUSAL İÇ HASTALIKLARI KONGRESİ, Antalya, Turkey, 8 December - 12 November 2023, (Full Text)

Primer İmmün Yetmezlik ve Amiloidoz

SOYAK AYTEKİN E., TAGİYEV A., SİLLELİ O., SAMUR İ., TEZCAN F. İ., ÇAĞDAŞ AYVAZ D. N.

8. KLİNİK İMMÜNOLOJİ KONGRESİ, Antalya, Turkey, 26 - 29 October 2022, (Summary Text)

INVESTIGATION OF COMBINED IMMUNODEFICIENCIES, IMMUNODEFICIENCIES WITH IMMUNEDYSREGULATION AND INNATE IMMUNE SYSTEM DEFECTS WITH ADVANCED IMMUNOLOGICAL AND GENETIC METHODS

ESENBOĞA S., HASKOLOĞLU Z. Ş., KELEŞ S., TAN Ç., GÜNER Ş. N., ÇAĞDAŞ AYVAZ D. N., et al.

World Allergy Congress, İstanbul, Turkey, 13 October 2022, pp.78, (Summary Text)

Central Nervous System Vasculitis in Primary Immune Deficiency

Uzunyayla-Sayici B., Oz S., GÖÇMEN R., TEZCAN F. İ., ÇAĞDAŞ AYVAZ D. N., ESENBOĞA S., et al.

Pediatric Neurology, Ankara, Turkey, 21 July 2022, (Full Text)

Enigma in Immune Dysregulation

ÇAĞDAŞ AYVAZ D. N.

The Joint Işıl Berat Barlan Symosium on Immunologic Disorders and The History of Medicine Meeting along with USERN Congress 2021, İstanbul, Turkey, 10 - 12 November 2021, (Full Text)

CMV Miyokarditi ve Ağır Hipotonisi Olan Bir Hastada ORAI1 Defekti

ESENBOĞA S., DEVECİ K., AKARSU A., OCAK M., BİLDİK H. N., YAZ İ., et al.

7. Klinik İmmünoloji Kongresi, Turkey, 6 - 09 October 2021, pp.64-65, (Summary Text)

MYH9 Eksikliği: Herediter Makrotrombositopeni Olgusu

ÖZBEK B., YAZ İ., ESENBOĞA S., BİLDİK H. N., AKARSU A., AKSU T., et al.

7. klinik İmmünoloji Kongresi, Turkey, 6 - 09 October 2021, vol.1, pp.63, (Summary Text)

Primer İmmün Yetmezlik Şüpheli Hastalarda DOCK8 Protein İfadesinin İncelenmesi

İnan D., OSKAY HALAÇLI S., YAZ İ., ESENBOĞA S., ÇAĞDAŞ AYVAZ D. N., TEZCAN F. İ.

7. klinik İmmünoloji Kongresi, Turkey, 6 - 09 October 2021, vol.1, pp.90, (Summary Text)

Immunodeficiencies affecting cellular and humoral immunity

ÇAĞDAŞ AYVAZ D. N.

Sixth European Journal of Immunology, Serbia, 31 August 2021, (Full Text)

A detailed analysis of regulatory T cell subpopulations in patients with autoimmune diseases

Inan D., Halacli S. O., Ayvaz D. N., Bolat A. B., Bildik H. N., Tezcan I.

vol.51, pp.316, (Summary Text)

Effects of CARMIL2 deficiency on functional and behavioral characteristics of immune cells

Yanik H., Horzum U., Aytekin E. S., Kursunel A., Tan C., Ozbek B., et al.

vol.51, pp.356, (Summary Text)

Characterization of altered innate immune responses of RLTPR deficient patient

Ibibik B., Evcili I., Bartan A., Tan C., Aytekin E. S., Ozbek B., et al.

vol.51, pp.327, (Summary Text)

Protein expression profiles in patients with primary immunodeficiencies

Halacli S. O., Cagdas D. N., Akarsu A., Kahveci M., Aytekin E. S., Inan D., et al.

vol.51, pp.364, (Summary Text)

Investigation of immune impairment status in primary immune deficiency

Evcili I., Kaya G. G., Ibibik B., Bartan A. G., Cetinkaya P. G., Gursel M., et al.

vol.51, pp.365, (Summary Text)