Prof.Dr. ELİF AYDINER

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome

Werren E. A., LaForce G. R., Srivastava A., Perillo D. R., Li S., Johnson K., et al.

Nature Communications , cilt.15, sa.1, 2024 (SCI-Expanded)

Rapamycin Controls Lymphoproliferation and Reverses T-Cell Responses in a Patient with a Novel STIM1 Loss-of-Function Deletion

Karakus I. S., Catak M. C., Frohne A., Bayram Catak F., Yorgun Altunbas M., Babayeva R., et al.

Journal of clinical immunology , cilt.44, sa.4, ss.94, 2024 (SCI-Expanded)

Evaluating the efficacy and safety of pozelimab in patients with CD55 deficiency with hyperactivation of complement, angiopathic thrombosis, and protein-losing enteropathy disease: an open-label phase 2 and 3 study

ÖZEN A. O., Chongsrisawat V., Sefer A. P., KOLUKISA B., Jalbert J. J., Meagher K. A., et al.

The Lancet , cilt.403, sa.10427, ss.645-656, 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 , cilt.25, sa.2, ss.282-293, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma

Evaluation of Clinical and Immunological Alterations Associated with ICF Syndrome

Bilgic Eltan S., Nain E., Catak M. C., Ezen E., Sefer A. P., Karimi N., et al.

Journal of Clinical Immunology , cilt.44, sa.1, 2024 (SCI-Expanded)

Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis

Kostel Bal S., Giuliani S., Block J., Repiscak P., Hafemeister C., Shahin T., et al.

Blood , cilt.142, sa.9, ss.827-845, 2023 (SCI-Expanded)

Severe allergic dysregulation due to a gain of function mutation in the transcription factor STAT6

BARIŞ S., Benamar M., Chen Q., Catak M. C., Martínez-Blanco M., Wang M., et al.

Journal of Allergy and Clinical Immunology , cilt.152, sa.1, ss.182, 2023 (SCI-Expanded)

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 , cilt.11, sa.1, 2023 (SCI-Expanded) Sürdürülebilir Kalkınma

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.

JOURNAL OF EXPERIMENTAL MEDICINE , cilt.220, sa.2, 2022 (SCI-Expanded)

Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry

Jamee M., Azizi G., BARIŞ S., Karakoc-Aydiner E., ÖZEN A. O., KILIÇ GÜLTEKİN S. Ş., et al.

CLINICAL IMMUNOLOGY , cilt.244, 2022 (SCI-Expanded)

Comparing the levels of CTLA-4-dependent biological defects in patients with LRBA deficiency and CTLA-4 insufficiency

Catak M. C., Akcam B., Bilgic Eltan S., Babayeva R., Karakus I. S., Akgun G., et al.

ALLERGY , cilt.77, sa.10, ss.3108-3123, 2022 (SCI-Expanded)

Increased radiosensitivity and impaired DNA repair in patients with STAT3-LOF and ZNF341 deficiency, potentially contributing to malignant transformations

Cekic S., Huriyet H., Hortoglu M., Kasap N., Ozen A. O., Karakoc-Aydiner E., et al.

CLINICAL AND EXPERIMENTAL IMMUNOLOGY , cilt.209, sa.1, ss.83-89, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Clinical and Laboratory Factors Affecting the Prognosis of Severe Combined Immunodeficiency

Ozturk E., Catak M. C., Kiykim A., Baser D., Bilgic Eltan S., Yalcin K., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.42, sa.5, ss.1036-1050, 2022 (SCI-Expanded)

Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency

Sefer A. P., Abolhassani H., Ober F., KAYAOĞLU B., Eltan S. B., Kara A., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.42, sa.3, ss.634-652, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Low Density Granulocytes and Dysregulated Neutrophils Driving Autoinflammatory Manifestations in NEMO Deficiency

Yilmaz N. S., Eltan S. B., KAYAOĞLU B., Geckin B., Heredia R. J., Sefer A. P., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.42, ss.582-596, 2022 (SCI-Expanded)

Food immunotherapy practice: Nation differences across Europe, The FIND project

Rodriguez del Rio P., Alvarez-Perea A., Blumchen K., Caimmi D., Christoph Caubet J., Panagiotis Konstantinopoulos A., et al.

ALLERGY , cilt.77, sa.3, ss.920-932, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

A boy with a novel homozygous ZAP70 mutation presenting with a dermatological phenotype and postnatal decrease in CD8(+) T cells

Babayeva R., Mongellaz C., Karakus I. S., Cansever M., Bilgic Eltan S., Catak M. C., et al.

PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.33, sa.3, 2022 (SCI-Expanded)

Evolution and long-term outcomes of combined immunodeficiency due to CARMIL2 deficiency

Kolukisa B., Baser D., Akcam B., Danielson J., Bilgic Eltan S., Haliloglu Y., et al.

ALLERGY , cilt.77, sa.3, ss.1004-1019, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Determining T and B Cell development by TREC/KREC analysis in primary immunodeficiency patients and healthy controls

Senturk G., Ng Y. Y., Eltan S. B., Baser D., Ogulur I., Altindirek D., et al.

SCANDINAVIAN JOURNAL OF IMMUNOLOGY , cilt.95, 2022 (SCI-Expanded)

Therapeutic options for CTLA-4 insufficiency.

Egg D., Rump I. C., Mitsuiki N., Rojas-Restrepo J., Maccari M., Schwab C., et al.

The Journal of allergy and clinical immunology , cilt.149, ss.736-746, 2022 (SCI-Expanded)

Primary antibody deficiencies in Turkey: molecular and clinical aspects

Firtina S., Ng Y. Y., HATIRNAZ NG Ö., Kiykim A., Ozek E. Y., Kara M., et al.

IMMUNOLOGIC RESEARCH , cilt.70, sa.1, ss.44-55, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory disease

Kubo S., Fritz J. M., Raquer-McKay H. M., Kataria R., Vujkovic-Cvijin I., Al-Shaibi A., et al.

NATURE IMMUNOLOGY , cilt.23, sa.1, ss.75-101, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

COVID-19 disease characteristics in different pediatric age groups

KEPENEKLİ KADAYİFCİ E., YAKUT N., Ergenc Z., Aydiner O., Sarinoglu R. C., KARAHASAN A., et al.

JOURNAL OF INFECTION IN DEVELOPING COUNTRIES , cilt.16, sa.1, ss.16-24, 2022 (SCI-Expanded)

Adverse COVID-19 outcomes in immune deficiencies: Inequality exists between subclasses.

AYDINER E., Eltan S. B., Babayeva R., Aydiner O., KEPENEKLİ KADAYİFCİ E., KOCAMIŞ B., et al.

Allergy , cilt.77, sa.1, ss.282-295, 2022 (SCI-Expanded)

Functions of NK and iNKT cells in pediatric and adult CVID, ataxia telangiectasia and agammaglobulinemia patients

Adin-Cinar S., Gelmez M. Y., Akdeniz N., Ozcit-Gurel G., KIYKIM A., Karakoc-Aydiner E., et al.

IMMUNOLOGY LETTERS , cilt.240, ss.46-55, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

Impaired respiratory burst contributes to infections in PKC-deficient patients

Neehus A., Moriya K., Nieto-Patlán A., Le Voyer T., Lévy R., Özen A. O., et al.

JOURNAL OF EXPERIMENTAL MEDICINE , cilt.218, sa.9, 2021 (SCI-Expanded)

Reference values for T and B lymphocyte subpopulations in Turkish children and adults.

Besci Ö., Başer D., Öğülür İ., Berberoğlu A. C., Kıykım A., Besci T., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.30, sa.51 (4), ss.1814-1824, 2021 (SCI-Expanded)

Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency

Aydemir S., Islek A., Nepesov S., Yaman Y., Baysoy G., Beser O. F., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.6, ss.1406-1410, 2021 (SCI-Expanded)

Single cell sequencing of peripheral mononuclear cells reveals CHAPLE-specific distinct signaling pathways

Ogulur I., Kim J., Ruckert B., Pat Y., AYDINER E., BARIŞ S., et al.

EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.372, 2021 (SCI-Expanded)

Adverse COVID outcomes in youngsters with immune deficiencies; inequality exists between subclasses

AYDINER E., Eltan S. B., Babayeva R., Aydiner O., KEPENEKLİ KADAYİFCİ E., KOLUKISA B., et al.

EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.285, 2021 (SCI-Expanded)

Reversal clinical and immunological effects of abatacept in patients with LRBA and CTLA4 deficiencies

BARIŞ S., Babayeva R., Catak M. C., Baser D., Eltan S. B., Akgun G., et al.

EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.77, 2021 (SCI-Expanded)

CHAPLE disease and non-CHAPLE protein losing enteropathies: natural history and immune characteristics

Selcuk M., Sefer A. P., Baser D., Ogulur I., Eltan S. B., Dursun E., et al.

EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.83, 2021 (SCI-Expanded)

Genomic investigation into early onset protein-losing enteropathies: therapeutic implications and insights into clusters of shared pathomechanisms

Sefer A. P., AYDINER E., Urganci N., Kiykim E., Baysoy G., Fisher M., et al.

EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.371, 2021 (SCI-Expanded)

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

ÇAĞDAŞ AYVAZ D. N., Mayr D., BARIŞ S., Worley L., Langley D. B., Metin A., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.6, ss.1272-1290, 2021 (SCI-Expanded)

Consensus Middle East and North Africa Registry on Inborn Errors of Immunity

Aghamohammadi A., Rezaei N., Yazdani R., Delavari S., KÜTÜKÇÜLER N., Topyildiz E., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, ss.1339-1351, 2021 (SCI-Expanded)

Autoinflammatory manifestations as a result of an elevated type I IFN signature in a case of NEMO deficiency

Yilmaz N. S., Eltan S. B., KAYAOĞLU B., Geckin B., Sozeri B., KIYKIM A., et al.

EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.51, ss.370, 2021 (SCI-Expanded)

Two patients with chronic mucocutaneous candidiasis caused by TRAF3IP2 deficiency

Shafer S., Yao Y., Comrie W., Cook S., Zhang Y., Yesil G., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.148, sa.1, ss.256-263, 2021 (SCI-Expanded)

GIMAP5 maintains liver endothelial cell homeostasis and prevents portal hypertension

Drzewiecki K., Choi J., Brancale J., Leney-Greene M. A., Sari S., Dalgiç B., et al.

JOURNAL OF EXPERIMENTAL MEDICINE , cilt.218, sa.7, 2021 (SCI-Expanded)

Lymphopenia with Low T and NK Cells in a Patient with USB1 Mutation, Rare Findings in Clericuzio-Type Poikiloderma with Neutropenia

Bilgic Eltan S., Sefer A. P., Karakus İ. S., ÖZEN A. O., Karakoc-Aydiner E., BARIŞ S.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.5, ss.1106-1111, 2021 (SCI-Expanded)

Stepwise Reversal of Immune Dysregulation Due to STAT1 Gain-of-Function Mutation Following Ruxolitinib Bridge Therapy and Transplantation

Kayaoglu B., Kasap N., Yilmaz N. S., Charbonnier L. M., Geckin B., Akcay A., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.4, ss.769-779, 2021 (SCI-Expanded)

Heterozygous AIRE Mutation in a Family with Multiple Autoimmune Organ Involvement

Sefer A. P., Kolukisa B. K., Akcam B., Demirkol Y. K., Aydiner E., Ozen A., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.41, sa.SUPPL 1, 2021 (SCI-Expanded)

Homozygous IL37 mutation associated with infantile inflammatory bowel disease

Zhang Z. Z., Zhang Y., He T., Sweeney C. L., Baris S., Karakoc-Aydiner E., et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA , cilt.118, sa.10, 2021 (SCI-Expanded)

Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

Meyts I., Bucciol G., Quinti I., Neven B., Fischer A., Seoane E., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.147, sa.2, ss.520-531, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

Broadly effective metabolic and immune recovery with C5 inhibition in CHAPLE disease

Ozen A. O., Kasap N., Vujkovic-Cvijin I., Apps R., Cheung F., Karakoc-Aydiner E., et al.

NATURE IMMUNOLOGY , cilt.22, sa.2, ss.128-151, 2021 (SCI-Expanded)

Reference values for T and B lymphocyte subpopulations in Turkish children and adults

Bescİ Ö., BaŞer D., ÖĞÜlÜr İ., BerberoĞlu A. C., Kiykim A., Bescİ T., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.51, sa.4, ss.1814-1824, 2021 (SCI-Expanded)

Prevalence of allergic disorders and risk factors associated with food allergy in Turkish preschoolers

Aksoy A. G., BORAN P., Karakoc-Aydiner E., Gokcay G., TAMAY Z. Ü., Devecioglu E., et al.

ALLERGOLOGIA ET IMMUNOPATHOLOGIA , cilt.49, sa.1, ss.11-16, 2021 (SCI-Expanded)

Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

Ghosh S., Köstel B., Edwards E., Pillay B., Jiménez H., Erol C., et al.

BLOOD , cilt.136, sa.23, ss.2638-2655, 2020 (SCI-Expanded)

Diagnostic Modalities Based on Flow Cytometry for Chronic Granulomatous Disease: A Multicenter Study in a Well-Defined Cohort

Baris H. E., Ogulur I., Akcam B., Kiykim A., Karagoz D., Saraymen B., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE , cilt.8, sa.10, ss.3525-3535, 2020 (SCI-Expanded)

Interleukin 12-23 deficiency in the interferon gamma pathway in a6-month-oldtoddler who hasBCGvaccine complications

BURSAL DURAMAZ B., TÜREL Ö., Akkoc G., Yozgat C. Y., Kasap N. A., AYDINER E., et al.

DERMATOLOGIC THERAPY , cilt.33, sa.6, 2020 (SCI-Expanded)

The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study

Cekic S., Metin A., Aytekin C., Edeer Karaca N., Baris S., Karali Y., et al.

PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.31, sa.5, ss.528-536, 2020 (SCI-Expanded)

Management of Systemic Hypersensitivity Reactions to Gonadotropin-Releasing Hormone Analogues during Treatment of Central Precocious Puberty

Kirkgoz T., Karakoc-Aydiner E., Bugrul F., Yavas Abali Z., Helvacioglu D., Kiykim A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.93, sa.1, ss.66-72, 2020 (SCI-Expanded)

Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score.

Tesch V., Abolhassani H., Shadur B., Zobel J., Mareika Y., Sharapova S., et al.

The Journal of allergy and clinical immunology , cilt.145, ss.1452-1463, 2020 (SCI-Expanded)

ILC3 deficiency and generalized ILC abnormalities in DOCK8-deficient patients

Eken A., Cansever M., Okus F. Z., Erdem S., Nain E., Azizoglu Z. B., et al.

Allergy: European Journal of Allergy and Clinical Immunology , cilt.75, sa.4, ss.921-932, 2020 (SCI-Expanded)

Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat

Kiykim A., Eker N., Surekli O., Nain E., Kasap N., Aktürk H., et al.

Pediatric Blood and Cancer , cilt.67, sa.2, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype

Nain E., ÜLGEN Ö., Kiykim A., Aydiner E., Ozen A. O., BARIŞ S.

CLINICAL IMMUNOLOGY , cilt.210, 2020 (SCI-Expanded)

Lymphocyte Subset Abnormalities in Pediatric-Onset Common Variable Immunodeficiency.

Ogulur I., Kiykim A., Baser D., Karakoc-Aydiner E., Ozen A. O., Baris S.

International archives of allergy and immunology , cilt.181, sa.3, ss.228-237, 2020 (SCI-Expanded)

Immune system defects in DiGeorge syndrome and association with clinical course.

Nain E., Kiykim A., ÖĞÜLÜR İ., Kasap N., Karakoc-Aydiner E., Ozen A. O., et al.

Scandinavian journal of immunology , cilt.90, sa.5, 2019 (SCI-Expanded)

Polymerase δ deficiency causes syndromic immunodeficiency with replicative stress.

Conde C. D., Petronczki Ö. Y., Baris S., Willmann K. L., Girardi E., Salzer E., et al.

The Journal of clinical investigation , cilt.129, sa.10, ss.4194-4206, 2019 (SCI-Expanded)

How to Approach Systemic Hypersensitivity reactions to Gonadotropin Releasing Hormone Analogues during treatment of Central Precocious Puberty

KIRKGÖZ T., Karakoc E., Kiykim A., Bugrul F., Helvacioglu D., Eltan S. B., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.185, 2019 (SCI-Expanded)

IFN-gamma stimulation of dental follicle mesenchymal stem cells modulates immune response of CD4(+) T lymphocytes in Der p1(+) asthmatic patients in vitro

Genç D., Zibandeh N., Nain E., Arığ Ü., Göker K., Aydıner E., et al.

ALLERGOLOGIA ET IMMUNOPATHOLOGIA , cilt.47, sa.5, ss.467-476, 2019 (SCI-Expanded)

A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency

Firtina S., Cipe F., Ng Y. Y., KIYKIM A., Ng O. H., Sudutan T., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.39, sa.2, ss.144-147, 2019 (SCI-Expanded)

Hematopoietic Stem Cell Transplantation in Patients with Heterozygous STAT1 Gain-of-Function Mutation.

Kiykim A., Charbonnier L. M., Akcay A., Karakoc-Aydiner E., Ozen A. O., Ozturk G., et al.

Journal of clinical immunology , cilt.39, sa.1, ss.37-44, 2019 (SCI-Expanded)

Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency.

Farmer J. R., Foldvari Z., Ujhazi B., De Ravin S. S., Chen K., Bleesing J. J., et al.

The journal of allergy and clinical immunology. In practice , cilt.7, sa.6, 2019 (SCI-Expanded)

Evaluation of a Standardized Bakery Product (SUTMEK) as a Potential Tool for Baked-Milk Tolerance and Immunotherapy Research Studies

Kiykim A., Karakoc-Aydiner E., Gunes E., Nain E., Öğülür İ., Yazici D., et al.

INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY , cilt.178, sa.1, ss.1-9, 2019 (SCI-Expanded)

Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency.

Kiykim A., Ogulur I., Dursun E., Charbonnier L. M., Nain E., Cekic S., et al.

The journal of allergy and clinical immunology. In practice , cilt.7, sa.8, 2019 (SCI-Expanded)

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry.

Maccari M. E., Abolhassani H., Aghamohammadi A., Aiuti A., Aleinikova O., Bangs C., et al.

Frontiers in immunology , cilt.9, ss.543, 2018 (SCI-Expanded)

Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study.

Barzaghi F., Hernandez L. C. A., Neven B., Ricci S., Kucuk Z. Y., Bleesing J. J., et al.

The Journal of allergy and clinical immunology , cilt.141, sa.3, 2018 (SCI-Expanded)

Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.

Petersen B., August D., Abt R., Alddafari M., Atarod L., BARIŞ S., et al.

Inflammatory bowel diseases , cilt.23, sa.12, ss.2109-2120, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

Prevalence of obesity in paediatric psoriasis and its impact on disease severity and progression.

Ergun T., SEÇKİN GENÇOSMANOĞLU D., Karakoc-Aydiner E., SALMAN A., Tekin B., BÜLBÜL BAŞKAN E., et al.

The Australasian journal of dermatology , cilt.58, sa.4, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

Predictive risk factors for relapse after cessation of inhaled corticosteroids in well-controlled childhood asthma

akturk h., Karakoc-Aydiner E., ÖZEN A. O., Baris S., akkoc T., bahceciler n., et al.

MINERVA PEDIATRICA , cilt.69, sa.4, ss.274-280, 2017 (SCI-Expanded)

CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis.

Ozen A. O., Comrie W. A., Ardy R. C., Conde C. D., Dalgıç B., Beser O. F., et al.

The New England journal of medicine , cilt.377, sa.1, ss.52-61, 2017 (SCI-Expanded)

Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication.

Aghamohammadi A., Hassan A., KÜTÜKÇÜLER N., Wassilak S. G., Pallansch M. A., Kluglein S., et al.

Frontiers in immunology , cilt.8, ss.685, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

Haploidentical Related Donor Hematopoietic Stem Cell Transplantation for Dedicator-of-Cytokinesis 8 Deficiency Using Post-Transplantation Cyclophosphamide.

Shah N. N., Freeman A. F., Su H., Cole K., Parta M., Moutsopoulos N. M., et al.

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation , cilt.23, sa.6, ss.980-990, 2017 (SCI-Expanded)

Basophil activation test for inhalant allergens in pediatric patients with allergic rhinitis.

ÖĞÜLÜR İ., Kiykim A., BARIŞ S., Ozen A. O., Yuce E. G., Karakoc-Aydiner E.

International journal of pediatric otorhinolaryngology , cilt.97, ss.197-201, 2017 (SCI-Expanded)

Could Sublingual Immunotherapy Affect Oral Health in Children with Asthma and/or Allergic Rhinitis Sensitized to House Dust Mite?

Kiykim A., MUMCU G., ÖĞÜLÜR İ., Karakoc-Aydiner E., Direskeneli H., BARIŞ S., et al.

INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY , cilt.174, sa.1, ss.52-56, 2017 (SCI-Expanded)

Severe Early-Onset Combined Immunodeficiency due to Heterozygous Gain-of-Function Mutations in STAT1

Baris S., Alroqi F., Kiykim A., Karakoc-Aydiner E., ÖĞÜLÜR İ., Ozen A. O., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.36, sa.7, ss.641-648, 2016 (SCI-Expanded)

School Board Policies on Prevention and Management of Anaphylaxis in İstanbul: Where Do We Stand?

ÖZEN A. O., BORAN P., torlak f., Karakoc-Aydiner E., barış s., KARAVUŞ M., et al.

Balkan medical journal , cilt.33, sa.5, ss.539-542, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

House Dust Mites Confer a Distinct Immunological Feature among Dermatitis

BARIŞ S., Ozen A. O., Akdeniz T., Karakoc-Aydiner E., Aydin O., ERCAN SARIÇOBAN H., et al.

IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY , cilt.15, sa.4, ss.264-274, 2016 (SCI-Expanded)

The effect of systemic corticosteroids on the innate and adaptive immune system in children with steroid responsive nephrotic syndrome.

Baris H. E., BARIŞ S., Karakoc-Aydiner E., GÖKCE İ., YILDIZ N., Cicekkoku D., et al.

European journal of pediatrics , cilt.175, sa.5, ss.685-93, 2016 (SCI-Expanded)

Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia.

Kiykim A., Garncarz W., Karakoc-Aydiner E., Ozen A. O., KIYKIM E., Yesil G., et al.

Clinical immunology (Orlando, Fla.) , cilt.165, ss.1-3, 2016 (SCI-Expanded)

Two patients with novel missense mutation in the purine nucleoside phosphorylase gene without serious or recurrent infections

Kiykim A., Simsek I. E., Kiykim E., Karakoc-Aydiner E., BARIŞ S., ÖZEN A. O., et al.

Clinical and Experimental Neuroimmunology , cilt.7, sa.1, ss.79-82, 2016 (SCI-Expanded)

Vitamin B12 deficiency among asymptomatic healthy infants: its impact on the immune system.

BORAN P., yildirim s., Karakoc Aydiner E., Ogulur I., ÖZEN A. O., Haklar G., et al.

Minerva pediatrica , 2016 (SCI-Expanded)

G6PC3 Deficiency: Primary Immune Deficiency Beyond Just Neutropenia

Kiykim A., BARIŞ S., Karakoc-Aydiner E., ÖZEN A. O., ÖĞÜLÜR İ., Bozkurt S., et al.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY , cilt.37, sa.8, ss.616-622, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

Nebulized fluticasone propionate, a viable alternative to systemic route in the management of childhood moderate asthma attack: A double-blind, double-dummy study.

Demirca B. P., Cagan H., Kiykim A., Arig U., Arpa M., Tulunay A., et al.

Respiratory medicine , cilt.109, sa.9, ss.1120-5, 2015 (SCI-Expanded)

Potentially Beneficial Effect of Hydroxychloroquine in a Patient with a Novel Mutation in Protein Kinase Cδ Deficiency.

Kiykim A., ÖĞÜLÜR İ., BARIŞ S., Salzer E., Karakoc-Aydiner E., ÖZEN A. O., et al.

Journal of clinical immunology , cilt.35, sa.6, ss.523-6, 2015 (SCI-Expanded)

AUTOIMMUNE DISEASE. Patients with LRBA deficiency show CTLA4 loss and immune dysregulation responsive to abatacept therapy.

Lo B., Zhang K., Lu W., Zheng L., Zhang Q., Kanellopoulou C., et al.

Science (New York, N.Y.) , cilt.349, sa.6246, ss.436-40, 2015 (SCI-Expanded)

Normative Data of Thyroid Volume-Ultrasonographic Evaluation of 422 Subjects Aged 0-55 Years

Aydiner O., AYDINER E., Akpinar I., Turan S., BEREKET A.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.2, ss.98-101, 2015 (SCI-Expanded)

JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family.

Baris S., Karakoc-Aydiner E., Ozen A. O., Delil K., Kiykim A., Ogulur I., et al.

Journal of clinical immunology , cilt.35, sa.4, ss.339-43, 2015 (SCI-Expanded)

Long-Term Effect of Sublingual and Subcutaneous Immunotherapy in Dust Mite-Allergic Children With Asthma/Rhinitis: A 3-Year Prospective Randomized Controlled Trial.

Karakoc-Aydiner E., Eifan A., BARIŞ S., Gunay E., Akturk E., AKKOÇ T., et al.

Journal of investigational allergology & clinical immunology , cilt.25, sa.5, ss.334-42, 2015 (SCI-Expanded)

Clinical Heterogeneity of Immunodysregulation, Polyendocrinopathy, Enteropathy, X-linked: Pulmonary Involvement as a Non-Classical Disease Manifestation

BARIŞ S., Schulze I., Ozen A. O., AYDINER E., Altuncu E., Karasu G. T., et al.

JOURNAL OF CLINICAL IMMUNOLOGY , cilt.34, sa.6, ss.601-606, 2014 (SCI-Expanded)

Vitamin D as an adjunct to subcutaneous allergen immunotherapy in asthmatic children sensitized to house dust mite.

Baris S., Kiykim A., Ozen A. O., Tulunay A., Karakoc-Aydiner E., Barlan I. B.

Allergy , cilt.69, sa.2, ss.246-53, 2014 (SCI-Expanded)

Alteration in humoral immunity is common among family members of patients with common variable immunodeficiency.

Karakoc-Aydiner E., ÖZEN A. O., Bans S., ercan h., ozdemir c., barlan i. b.

Journal of investigational allergology & clinical immunology , cilt.24, sa.5, ss.346-51, 2014 (SCI-Expanded)

Identification of a novel mutation in ZAP70 and prenatal diagnosis in a Turkish family with severe combined immunodeficiency disorder

Karaca E., Karakoc-Aydiner E., BAYRAK Ö. F., Keles S., Sevli S., Barlan I. B., et al.

GENE , cilt.512, sa.2, ss.189-193, 2013 (SCI-Expanded)

Inhaled alpha 1-Antitrypsin Administered to Treat Pneumatocele in Autosomal Dominant Hyperimmunoglobulin E Syndrome

Karakoc-Aydiner E., Baris S., Keles S., Ozdemir C., Chatila T., Barlan I.

JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY , cilt.23, sa.5, ss.359-361, 2013 (SCI-Expanded)

The phenotype-genotype relationship in severe congenital neutropenia patients

BARIŞ S., Aydiner E., Kiykim A., Çaǧan H. H., Boztug K., Barlan I.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.47, sa.4, ss.272-277, 2012 (SCI-Expanded)

Pitfalls in the diagnosis of thyroid dysgenesis by thyroid ultrasonography and scintigraphy

Karakoc-Aydiner E., Turan S., Akpinar I., Dede F., Isguven P., Adal E., et al.

EUROPEAN JOURNAL OF ENDOCRINOLOGY , cilt.166, sa.1, ss.43-48, 2012 (SCI-Expanded)

Osteoporosis: An ignored complication of CVID

BARIŞ S., Ozen A. O., ERCAN SARIÇOBAN H., Karakoc-Aydiner E., Cagan H., Ozdemir C., et al.

PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.22, sa.7, ss.676-683, 2011 (SCI-Expanded)

A novel approach in allergen-specific immunotherapy: Combination of sublingual and subcutaneous routes

Keles S., Karakoc-Aydiner E., Ozen A. O., Izgi A. G., Tevetoglu A., AKKOÇ T., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.128, sa.4, ss.808-822, 2011 (SCI-Expanded)

Serum immunoglobulin levels as a predictive factor for a better outcome of non-atopic childhood asthma

BARIŞ S., Karakoc-Aydiner E., Ozen A. O., Ozdemir C., Bahceciler N. N., Barlan I. B.

PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.22, sa.3, ss.298-304, 2011 (SCI-Expanded)

An Adolescent with Hyperimmunoglobulinemia D and Periodic Fever Syndrome Responding to Simvastatin Treatment

Karakoç-Aydiner E., Özdemir C., Keleş S., BARIŞ S., Bahçeciler N. N., Barlan I. B.

TURKISH JOURNAL OF RHEUMATOLOGY , cilt.26, sa.2, ss.167-170, 2011 (SCI-Expanded)

Efficacy of Intravenous Immunoglobulin Treatment in Children with Common Variable Immunodeficiency

BARIŞ S., ercan h., cagan h., ÖZEN A. O., Karakoc-Aydiner E., Ozdemir C., et al.

JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY , cilt.21, sa.7, ss.514-521, 2011 (SCI-Expanded)

Outcome of hypogammaglobulinemia in children: Immunoglobulin levels as predictors

ÖZEN A. O., Baris S., Karakoc-Aydiner E., Ozdemir C., Bahceciler N., Barlan I.

CLINICAL IMMUNOLOGY , cilt.137, sa.3, ss.374-383, 2010 (SCI-Expanded)

Neonatal BCG vaccination induces IL-10 production by CD4+CD25+T cells

AKKOÇ T., Aydogan M., Yildiz A., Karakoc-Aydiner E., Eifan A., Keles S., et al.

PEDIATRIC ALLERGY AND IMMUNOLOGY , cilt.21, sa.7, ss.1059-1063, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome

Engelhardt K. R., McGhee S., Winkler S., Sassi A., Woellner C., Lopez-Herrera G., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.124, sa.6, ss.1289-1302, 2009 (SCI-Expanded)

Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

Al Khatib S., Keles S., Garcia-Lioret M., Koc-Aydiner E., Reisli I., ARTAÇ H., et al.

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY , cilt.124, sa.2, ss.342-348, 2009 (SCI-Expanded)

Familial thyroid dysgenesis: Which genes could be involved?

Castenet M., Carre A., BEREKET A., Guney I., AYDINER E., Turan S., et al.

HORMONE RESEARCH , cilt.70, ss.163, 2008 (SCI-Expanded)

Polymorphisms in the vitamin D receptor gene in children with idiopathic hypercalcemia

Guney I., Turan S., Sevinc D., GÜRAN T., Akcay T., Karakoc E., et al.

HORMONE RESEARCH , cilt.70, ss.49, 2008 (SCI-Expanded)

Screening of Parents and Siblings of Patients with Thyroid Dysgenesis by Thyroid Function Tests and Ultrasound

Karakoc E., Turan S., Akpinar I., Isguven P., Adal E., Haklar G., et al.

HORMONE RESEARCH , cilt.70, sa.6, ss.329-339, 2008 (SCI-Expanded)

Screening of parents and siblings of children with thyroid dysgenesis by thyroid function tests and ultrasound

Aydiner E., Turan S., Akpinar I., Isguven P., Adal E., Akcay T., et al.

HORMONE RESEARCH , cilt.65, ss.41, 2006 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

Single-Center Experience in Vaccination of Children in Special Risk Groups: A Multidisciplinary Institutional Consensus Protocol

BARIŞ H. E., Kepenekli E., Sakar F. İ. A., ÜTÜK B., ŞAHİN P., Ergenç Z., et al.

Turkish Archives of Pediatrics , cilt.58, sa.5, ss.531-538, 2023 (ESCI) Sürdürülebilir Kalkınma

Immunization practices in children with a history of allergies

Baris H. E., BORAN P., Kiykim A., BARIŞ S., Ozen A., AYDINER E.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.55, sa.3, ss.244-250, 2020 (ESCI) Sürdürülebilir Kalkınma

Lymphocyte Functions in Patients with Chronic Granulomatous Disease and Carrier Individuals

ÖĞÜLÜR İ., Barış E., KIYKIM A., Başer D., Akgün G., ÖZEN A. O., et al.

TURKISH JOURNAL OF IMMUNOLOGY , cilt.7, sa.2, ss.93-101, 2019 (ESCI)

The Diagnostic Value of Flow Cytometry in DOCK8 Deficiency

ÖĞÜLÜR İ., Kiykim A., Nain E., Kasap N., Akgün G., Karakoç-Aydiner E., et al.

TURKISH JOURNAL OF IMMUNOLOGY , cilt.7, sa.2, ss.102-106, 2019 (ESCI)

Kronik Granülomatöz Hastalarında ve Bu Hastalığı GenetikOlarak Taşıyan Bireylerde Lenfosit Fonksiyonları

BARIŞ S., KIYKIM A., ÖZEN A. O., AYDINER E., ÖĞÜLÜR İ., Akgün G., et al.

Türk İmmünoloji Dergisi , 2019 (Scopus)

Ev Tozu Akarı Duyarlı Atopik Dermatitli Çocuklarda D Vitaminin Etkisi

Nain E., KIYKIM A., YAŞÖZ C., BAYRAMLI R., BARIŞ S., ÖZEN A. O., et al.

Astım Allerji İmmünoloji , cilt.16, ss.40-46, 2018 (Hakemli Dergi)

Diagnostic Usage of Intracellular Protein Staining by Flow Cytometer in Primary Immune Deficiencies; Marmara Experience

ÖĞÜLÜR İ., BARIŞ S., Ozen A. O., Nain E., Kiykim A., Karakoc-Aydiner E.

ASTIM ALLERJI IMMUNOLOJI , cilt.16, sa.2, ss.81-89, 2018 (ESCI)

LRBA Eksikliği Tanısında Akan Hücre Ölçerde Protein İfadesi

oğulur i., KIYKIM A., Nain E., SOMER A., GÜVEN A., BARIŞ S., et al.

Astım Allerji İmmünoloji , cilt.15, ss.123-128, 2017 (Hakemli Dergi)

Serum IgE Düzeyi ve Eozinofil Sayısı ile AtopikHastalıklar Hiper IgE Sendromu’xxndan Ayırt Edilebilir mi?

KIYKIM A., YÜCE E. G., BARIŞ E., Nain E., KELEŞ S., AKTÜRK H., et al.

Astım Allerji İmmünoloji , cilt.15, ss.1-9, 2017 (Hakemli Dergi)

Can Atopic Diseases be Differentiated from Hyper IgE Syndrome by Serum IgE and Blood Eosinophil Levels?

Kiykim A., Yuce E. G., Baris E., Nain E., KELEŞ S., Akturk H., et al.

ASTIM ALLERJI IMMUNOLOJI , cilt.15, sa.2, ss.73-81, 2017 (ESCI)

Protein Expression in the Diagnosis of LRBA Deficiency by Flow Cytometer

ÖĞÜLÜR İ., Kiykim A., Nain E., Somer A., Guven A., BARIŞ S., et al.

ASTIM ALLERJI IMMUNOLOJI , cilt.15, sa.3, ss.123-128, 2017 (ESCI)

The plethora, clinical manifestations and treatment options of autoimmunity in patients with primary immunodeficiency.

Baris H. E., Kiykim A., Nain E., ÖZEN A. O., Karakoc-Aydiner E., BARIŞ S.

Turk pediatri arsivi , cilt.51, sa.4, ss.186-192, 2016 (ESCI)

Nijmegen-Breakage Syndrome; Two Siblings Presenting with Different Phenotypes

Kiykim A., AYDINER E., ÖĞÜLÜR İ., BARIŞ S., Ozen A. O., Serifov K., et al.

ASTIM ALLERJI IMMUNOLOJI , cilt.14, sa.2, ss.98-102, 2016 (ESCI)

Primary catastrophic antiphospholipid syndrome in an 8 year old girl

BARIŞ H. E., AKSU LİMON Ç., VURAL I., KEPENEKLİ KADAYİFCİ E., KOÇ A., KIYKIM A., et al.

MARMARA MEDICAL JOURNAL , cilt.29, sa.1, ss.41, 2016 (ESCI)

Use of subcutaneous immunoglobulin in primary immune deficiencies

AYDINER E., Kiykim A., BARIŞ S., Ozen A. O., Barlan I.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.51, sa.1, ss.8-14, 2016 (ESCI)

A patient with mushroom allergy; A new etiological agent of Kounis syndrome Mantar allerjisi olan bir olgu; Kounis sendromuna neden olan yeni bir etyolojik ajan

Tepetam F. M., Dağdeviren B., Bulut İ., Karabay C. Y., BARIŞ S., Aydiner Karakoç E.

Tuberkuloz ve Toraks , cilt.64, sa.2, ss.171-174, 2016 (ESCI)

Hiperimmünglobulin M sendromunun akan hücre ölçer ile değerlendirilmesi Evaluation of Hyperimmunoglobulin M syndrome by flow cytometry

ÇINAR S., GELMEZ M. Y., Safa B., AYDINER E., ÖZEN A. O., Hacer A., et al.

Turk J Immunol , 2015 (Hakemli Dergi)

Dihidrorodamin testi ile oksidatif patlama Sağlıklı kontrollerde referans değerleri Oxidative burst with Dihyrrhodamine test Reference values in healthy controls

Dilek Ç., ÖĞÜLÜR İ., AYDINER E., Safa B., ÖZEN A. O., Işıl B.

Turk J Immunol , 2015 (Hakemli Dergi)

The Effect of Vitamin D Supplementation on Subcutaneous Allergen Immunotherapy in House Dust Mite Sensitive Asthmatic Children

Baris S., Ozen A. O., Cagan H., Kiykim A., Tulunay A., Karakoc-Aydiner E., et al.

TURKISH JOURNAL OF IMMUNOLOGY , cilt.3, sa.2, ss.54-63, 2015 (ESCI)

Oxidative Burst with Dihydrorhodamine Test: Reference Values in Healthy Controls

Cicekkoku D., ÖĞÜLÜR İ., Karakoc-Aydiner E., BARIŞ S., Kiykim A., Ozen A. O., et al.

TURKISH JOURNAL OF IMMUNOLOGY , cilt.3, sa.2, ss.49-53, 2015 (ESCI)

Ev Tozu Akarı duyarlı Astımlı çocuklarda Subkutan Allerjen İmmünoterapi üzerine D Vitaminin etksis The effect of Vitamin D supplementation on subcutaneous allergen immunotherapy in house dust mite sensitive asthmatic children

ÇINAR S., GELMEZ M. Y., Safa B., AYDINER E., ÖZEN A. O., Hacer A., et al.

Turk J Immunol , 2015 (Hakemli Dergi)

Dihidrorhodamin Testi ile Oksidatif Patlama Sağlıklı KontrollerdeReferans Değerleri

ÇİÇEKKÖKÜ D., ÖĞÜLÜR İ., AYDINER E., BARIŞ S., KIYKIM A., ÖZEN A. O., et al.

Turk J Immunol , 2015 (Hakemli Dergi)

Evaluation of Hyperimmunoglobulin M Syndrome by Flow Cytometry

Cinar S., Gelmez M. Y., BARIŞ S., AYDINER E., ÖZEN A. O., Akturk H., et al.

TURKISH JOURNAL OF IMMUNOLOGY , cilt.3, sa.2, ss.64-70, 2015 (ESCI)

Atypical presentation of Takayasu's arteritis in an adolescent

Binnetoglu K. K., Karakoc Aydiner E., BARIŞ S., Ozen A. O., Zohre A. I., BALTACIOĞLU F., et al.

MARMARA MEDICAL JOURNAL , cilt.28, sa.3, ss.157-160, 2015 (ESCI) Sürdürülebilir Kalkınma

Early-onset neurolupus: A challenge for pediatricians

BARIŞ S., Karakoc-Aydiner E., Ozen A. O., Kacmaz M., Namar M., YILDIZ N., et al.

MARMARA MEDICAL JOURNAL , cilt.28, sa.2, ss.105-108, 2015 (ESCI)

Kronik granülomatöz hastalıklı olgularımızın değerlendirilmesi

BARIŞ S., ÖZEN A. O., KIYKIM A., onat e. g., AYDINER E., BARLAN I.

ASTIM ALLERJI IMMUNOLOJI , ss.26-34, 2014 (Hakemli Dergi)

The evaluation of our patients with chronic granulomatous disease

BARIŞ S., ÖZEN A. O., KIYKIM A., Onat E. G., Aydiner E., Barlan I.

ASTIM ALLERJI IMMUNOLOJI , cilt.12, sa.1, ss.26-34, 2014 (ESCI)

Lymphocyte proliferation in common variable immunodeficiency (CVID) patients by carboxyfluorescein succinimidyl ester (CFSE)

Izgi A., AKKOÇ T., Ogulur I., Tevetoglu A., AYDINER E., BARIŞ S., et al.

CLINICAL AND EXPERIMENTAL HEALTH SCIENCES , cilt.1, sa.3, ss.171-177, 2011 (ESCI)

Investigation of Th17 cell differentiation in immunodeficiencies associated with high IgE levels and/or autoimmunity

AKKOÇ T., Tevetoglu A., Ogulur I., Izgi A., AYDINER E., BARIŞ S., et al.

CLINICAL AND EXPERIMENTAL HEALTH SCIENCES , cilt.1, sa.2, ss.96-102, 2011 (ESCI)

Bloom syndrome: presentation of two siblings

BARIŞ S., AYDINER E., ÖZEN A. O., ÖZDEMİR C., Bahceciler N. N., Barlan I. B.

ASTIM ALLERJI IMMUNOLOJI , cilt.8, sa.1, ss.64-68, 2010 (ESCI)

Long term follow-up of hyperimmunoglobulin M syndrome cases

AYDINER E., ÖZDEMİR C., Keles S., BARIŞ S., Cinar S. A., DENİZ G., et al.

ASTIM ALLERJI IMMUNOLOJI , cilt.8, sa.2, ss.101-107, 2010 (ESCI)

Rehospitalization rates of infants of less than 32 weeks gestation in the first year of life

AYDINER E., Akman I. Ö., Kalaça S., Ünver T., Bilgen H. S., ÖZEK E.

Marmara Medical Journal , cilt.18, sa.2, ss.71-75, 2005 (Scopus)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Primer Antikor Yetersizliği Olan Hastalarda Saptanan Bruton Tirozin Kinaz (BTK) Gen Varyasyonları

Firtina S., NG Y. Y., HATIRNAZ NG Ö., HASKOLOĞLU Z. Ş., Kıykım A., AYDINER E., et al.

24. Ulusal İmmünoloji Kongresi, Türkiye, 27 Nisan 2017 - 30 Nisan 2027

Delayed Umbilical Cord Separation and Associated Factors

AYGÜN B., BARIŞ H. E., BARIŞ S., ÖZEN A. O., AYDINER E., BORAN P.

3rd International Eurasian Congress of Social Pediatrics& 7th National Congress of Social Pediatrics, İzmir, Türkiye, 16 - 20 Kasım 2022

Allergic Diseases in Children with Behavioral Insomnia of Childhood

TORUN T., BARIŞ H. E., ÖZBÖRÜ AŞKAN Ö., ÖZEN A. O., BARIŞ S., AYDINER E., et al.

3rd International Eurasian Congress of Social Pediatrics& 7th National Congress of Social Pediatrics, İzmir, Türkiye, 16 - 20 Kasım 2022

ÇOCUKLUK ÇAĞI DAVRANIŞSAL İNSOMNİSİNDE ALLERJEN DUYARLILIK VE HASTALIK SIKLIĞI

TORUN T., BARIŞ H. E., ÖZBÖRÜ AŞKAN Ö., ÖZEN A. O., BARIŞ S., AYDINER E., et al.

57. TÜRK PEDİATRİ KONGRESİ, Kıbrıs (Kktc), 22 - 26 Mayıs 2022

BESİN ALERJİSİ OLAN ÇOCUKLARDA YAŞAM KALİTESİ VE TEDAVİ MEMNUNİYETİNİN DEĞERLENDİRİLMESİ

GÜNAL Ö., SEFER A. P., ÜTÜK B., BİLGİÇ ELTAN S., YORĞUN ALTUNBAŞ M., BARIŞ S., et al.

57. TÜRK PEDİATRİ KONGRESİ, Türkiye, 22 Mayıs 2022, ss.307-310

Besin Alerjisi Tanısına Göre Ebeveynlerin Besin Satın Alma Alışkanlıklarının Karşılaştırılması

ÇELİK Z. M., AYDINER E., FERELİ S., AKTAÇ Ş., GÜNEŞ F. E.

GIDA ALERJENLERİ, BULAŞANLARI ve HALK SAĞLIĞI AÇISINDAN ÖNEMİ (GABS2021), Türkiye, 24 Haziran 2021

The evaluation of radiosensitivity in patients with STAT3 deficiency

ÇEKİÇ Ş., Huriyet H., Hortoglu M. B., BARIŞ S., METİN A., ÖZEN A. O., et al.

the 12th Annual Meeting of the Clinical Immunology Society: 2021 Virtual Annual Meeting: Immune Deficiency and Dysregulation North American Conference, 14 Nisan 2021

Broadly Effective Metabolic And Immune Recovery With C5 inhibition in CHAPLE Disease.

ÖZEN A. O., ÖĞÜLÜR İ., BARIŞ S., AYDINER E.

19th Biennial Meeting of The European Society for Immunodeficiencies., Birmingham, Birleşik Krallık, 14 - 16 Ekim 2020

EXTENDED CLINICAL AND IMMUNOLOGICAL PHENOTYPE AND TRANSPLANT OUTCOME INCD27 AND CD70 DEFICIENCY

GHOSH S., Bal S. K., EDWARDS E. J., HEREDİA JİMENEZ R., PİLLAY B., ÇİPE F., et al.

19. Biennial Meeting of ESID, ONLİNE, Birleşik Krallık, 14 - 17 Ekim 2020

Dramatic metabolic recovery following precision therapy of CHAPLE syndrome.

ÖZEN A. O., ŞAHİN AKKELLE B., ÖĞÜLÜR İ., GÜNER Ş. N., AYDINER E., BARIŞ S., et al.

World Immune Regulation Meeting. Dramatic metabolic recovery following precision therapy of CHAPLE syndrome., DAVOS, İsviçre, 04 Ekim 2020

Functional analysis of inflammation associated parameters in a case of NEMO deficiency before and after HSCT

Surucu N., KAYAOĞLU B., Geckin B., Ayanoglu I. C., Eltan S. B., Kasap N., et al.

17th International Congress of Immunology of the International-Union-of-Immunological-Societies (IUIS), Beijing, Çin, 19 - 23 Ekim 2019, cilt.49, ss.1232-1233

Polymerase delta deficiency causes syndromic immunodeficiency with replicative stress

Conde D., Petronczki Ö., BARIŞ S., Willmann K., Girardi E., Salzer E., et al.

2nd European Society for Immunodeficiencies Focused Meeting, 18 - 21 Eylül 2019

MMR immunisation practices in children with a history of egg allergy

Baris E., BORAN P., Kiykim A., Safa B., Ahmet O., Karakoc-Aydiner E.

Congress of the European-Academy-of-Allergy-and-Clinical-Immunology (EAACI), Lisbon, Portekiz, 1 - 05 Haziran 2019, cilt.74, ss.895

Treatment forms and clinical course of LPS-Responsive beige-like anchor protein deficiency and introduction of the immune deficiency and -dysregulation activity (=IDDA) score

Tesch V. K., Abolhassani H., Grimbacher B., Lankaster A., Gennery A., Shadur B., et al.

45th Annual Meeting of the European-Society-for-Blood-and-Marrow-Transplantation (EBMT), Frankfurt, Almanya, 24 - 27 Mart 2019, cilt.54, ss.98-99

Schoolboard policies on prevention and management of anaphylaxis in Istanbul? Where do we stand?

ÖZEN A. O., BORAN P., torlak F., Eltan Bilgiç S., Baris S., KARAVUŞ M., et al.

EAACI 2019, 1 - 05 Haziran 2019

DIMINISHED CELL NUMBER AND FUNCTION OF NATURAL KILLER CELLS IN LRBA DEFICIENT PATIENTS

ÇINAR S., GELMEZ M. Y., AKDENİZ N., Özçit G., Kıykım A., AYDINER E., et al.

International Molecular Immunology Immunogenetics Congress IV (MIMIC IV), Bursa, Türkiye, 27 - 29 Nisan 2019, ss.120

IgE PRODUCTION IN CHRONIC GRANULOMATOUS DISEASE RELATED TO FUNGAL ANTIGENIC STIMULATION

ÖĞÜLÜR İ., AYDINER E., BARIŞ S., ÖZEN A. O., KIYKIM A.

MIMIC IV, 27 - 29 Nisan 2019

Betalaktam Antibiyotiklerle Allerji Öyküsü Pozitif 29 Çocukta Deri Testlerinde Reaksiyon Oranı Sadece20

Bilgiç Eltan S., KASAP N., KOCAMIŞ B., KIYKIM A., NAİN E., CAVKAYTAR Ö., et al.

14. Uluslararası Katılımlı Çocuk Allerji ve Astım Kongresi, Antalya, Türkiye, 22 - 25 Nisan 2019

Immunisation practices in children with a history of allergies

Barış H. E., BORAN P., KIYKIM A., BARIŞ S., ÖZEN A. O., AYDINER E.

1st International Eurasian Congress of Social Pediatrics, 01 Aralık 2018

CHAPLE Hastalığında Eritro-Lökosit Agregasyonu Belirteç Olarak Kullanılabilir Mi?

Akgün G., Başer D., AYDINER E., ÖĞÜLÜR İ., Kasap N., Bilgiç Eltan S., et al.

XXV. Ulusal Allerji ve Klinik İmmünoloji Kongresi, Antalya, Türkiye, 17 - 21 Kasım 2018

Akan Hücre ile CD55 Eksikliği Hastalığı Taraması

ÖĞÜLÜR İ., SARI S., KIYKIM A., Akgün G., NAİN E., TUTAR E., et al.

XXV. Ulusal Allerji ve Klinik İmmünoloji Kongresi, Antalya, Türkiye, 17 - 21 Kasım 2018

Kronik Granülomatöz Hastalıkta Akan Hücre Ölçerde Belirlenen NADPH Oksidaz Enzim Aktivitesinin ve Alt Ünitelerinin Genotipi Öngörmede Rolü

Akçam B., Barış E., ÖĞÜLÜR İ., Kasap N., Bilgiç Eltan S., Başer D., et al.

XXV. Ulusal Allerji ve Klinik İmmünoloji Derneği, Antalya, Türkiye, 17 - 21 Kasım 2018

Ataksi Telenjiektazi Hastalarının Ebeveynlerinde Enfeksiyonlar ve Lenfosit Alt Grup Bozuklukları

ÖĞÜLÜR İ., Ertüzün T., ÖZEN A. O., UYAR E., KIYKIM A., Başer D., et al.

XXV. Ulusal Allerji ve Klinik İmmünoloji Kongresi, Antalya, Türkiye, 17 - 21 Kasım 2018

Dihidrorhodamin Testinde Yanlış Pozitiflik ile Tanınan Bir MPO Eksikliği Olgusu

Başer D., BARIŞ S., Türe Özdemir F., ÖĞÜLÜR İ., Kasap N., Bilgiç Eltan S., et al.

XXV. Ulusal Allerji ve Klinik İmmünoloji Kongresi, Antalya, Türkiye, 17 - 21 Kasım 2018

MOTHERS OF AUTOSOMAL RECESSIVE CHRONIC GRANULOMATOUS DISEASE PATIENTS DO NOT SHOW AUTOIMMUNE FINDINGS IN CONTRAST TO X-LINKED PATIENTS

Barış E., KIYKIM A., NAİN E., Aksoy G., ÖĞÜLÜR İ., Başer D., et al.

18th Biennial Meeting of ESID, Lizbon, Portekiz, 24 - 27 Ekim 2018

INTRACELLULAR STAINING OF SUBUNITS OF NADPH OXIDASE ENZYME PREDICTS DEFECTIVE GENE IN PATIENTS WITH CHRONIC GRANULOMATOUS DISEASE

Barış E., ÖĞÜLÜR İ., Akçam B., Başer D., KIYKIM A., Kasap N., et al.

18th Biennial Meeting of ESID, Lizbon, Portekiz, 24 - 27 Ekim 2018

IS IT POSSIBLE TO DISTINGUISH TRUE LRBA PATIENTS WITH THE EXPRESSION OF THE LRBA PROTEIN BY FLOW CYTOMETER?

ÖĞÜLÜR İ., KIYKIM A., AYDINER E., BARIŞ S., ÖZEN A. O.

18th Biennial Meeting of ESID, Lizbon, Portekiz, 24 - 27 Ekim 2018

IMMUNOPHENOTYPING DIFFERENCES IN HYPER-IGE SYNDROMES ASSOCIATED WITH DOCK8 AND STAT3 MUTATIONS?

Başer D., ÖĞÜLÜR İ., KIYKIM A., Kasap N., NAİN E., BARIŞ S., et al.

18th Biennial Meeting of ESID, Lizbon, Portekiz, 24 - 27 Ekim 2018

A FLOW-CYTOMETRY BASED SCREENING FOR CD55 DEFICIENCY IS A RAPID

ÖĞÜLÜR İ., SARI S., KIYKIM A., NAİN E., TUTAR E., AYDINER E., et al.

18TH BIENNIAL MEETING OF THE EUROPEAN SOCIETY FOR IMMUNODEFICIENCIES (ESID) 2018, 24 - 27 Ekim 2018

CD55 MEDIATED LOSS OF CO-STIMULATION CAUSES INSUFFICIENT IL10 PRODUCTION IN PATIENTS WITH CD55

ÖZEN A. O., ÖĞÜLÜR İ., KIYKIM A., BARIŞ S., AYDINER E.

18th Biennial Meeting of ESID, Lizbon, Portekiz, 24 - 27 Ekim 2018

A TURKISH LRBA DEFICIENCY COHORT PROVIDING CLINICAL AND LABORATORYUTILITIES

KIYKIM A., DURSUN E., NAİN E., ÇEKİÇ Ş., ÖĞÜLÜR İ., BAŞER D., et al.

The 18th Biennial Meeting of ESID, Lizbon, Portekiz, 24 - 27 Ekim 2018

POTENTIAL ROLE OF NATURAL KILLER CELLS IN LRBA DEFICIENCY

ÇINAR S., GELMEZ M. Y., AKDENİZ N., Ozcit G., KIYKIM A., ÖZEN A. O., et al.

18th ESID, 24 - 27 Ekim 2018

INFECTIONS AND LYMPHOCYTE SUBSET ALTERATIONS IN ATAXIA TELANGIECTASIA MUTATED KINASE CARRIERS

ÖĞÜLÜR İ., Ertüzün T., ÖZEN A. O., UYAR E., KIYKIM A., Başer D., et al.

18th Biennial Meeting of ESID, Lizbon, Portekiz, 24 - 27 Ekim 2018

LRBA eksikliğinde CTLA-4 analoğunun (abatacept) lenfosit alt tipleri üzerine ex-vivo etkileri

KIYKIM A., ÖĞÜLÜR İ., Dursun E., YILDIRAN A., UNCUOĞLU A., KELEŞ S., et al.

İmmünolojide Moleküller Sempozyumu, İzmir, Türkiye, 18 - 21 Ekim 2018

Cytokine patterns and impaired cytotoxic activity of NK cells in children with atopic dermatitis

ÇETİN E., AKDENİZ N., Baris S., AYDINER E., BARLAN I., DENİZ G.

Abstracts of the 5th European Congress of Immunology, Amsterdam, Hollanda, 2 - 05 Eylül 2018

Evaluation of a standardized bakery product (SUTMEK) as a potential tool for baked milk tolerance and immunotherapy research studies

KIYKIM A., AYDINER E., GÜNEŞ F. E., NAİN E., ÖĞÜLÜR İ., AKTAÇ Ş., et al.

European Academy of Allergy and Clinical ImmunologyCongress, Munich, Almanya, 26 - 30 Mayıs 2018, cilt.73

The effect of high dose vitamin‐D onlymphocytes in children with atopic dermatitis

ÖĞÜLÜR İ., ÖZEN A. O., NAİN E., KIYKIM A., BARIŞ S., AYDINER E.

European Academy of Allergy and Clinical ImmunologyCongress, 26 - 30 Mayıs 2018, cilt.73

Approaches of patients receiving subcutaneous immunotherapy to anaphylaxis

Saricoban E. H., Karakoc-Aydiner E.

Congress of the European-Academy-of-Allergy-and-Clinical-Immunology (EAACI), Munich, Almanya, 26 - 30 Mayıs 2018, cilt.73, ss.849

SOTI in IgE mediated cow's milk allergy, two case reports

Kasap N., Kiykim A., Karakoc-Aydiner E., Ozen A. O., Baris S.

Congress of the European-Academy-of-Allergy-and-Clinical-Immunology (EAACI), Munich, Almanya, 26 - 30 Mayıs 2018, cilt.73, ss.842

Evaluation of a standardized bakery product (SUTMEK) as a potential tool for baked milk tolerance and immunotherapy research studies

Kiykim A., Karakoc-Aydiner E., Gunes E., Nain E., ÖĞÜLÜR İ., AKTAÇ Ş., et al.

Congress of the European-Academy-of-Allergy-and-Clinical-Immunology (EAACI), Munich, Almanya, 26 - 30 Mayıs 2018, cilt.73, ss.122-123

Eosinophilia: Lessons from primary immunodeficiencies, Hall 14a, 28 May, 15:45-16:15, Severe combined primary immunodeficiencies with eosinophilia

AYDINER E.

EAACI 2018, Munich, Almanya, 27 - 31 Mayıs 2018

Group 3 innate lymhoid cells are absent in DOCK8-defective HIES patients

EKEN A., Okus F. Z., Patiroglu T., Erdem S., KARAKÜKCÜ M., Cansever M., et al.

Annual Meeting of the American-Association-of-Immunologists (AAI), Texas, Amerika Birleşik Devletleri, 4 - 08 Mayıs 2018, cilt.200

Detection of T-cell Receptor Excision Circles (TRECs) in Dried Blood Spot (DBS) Implementation of Routine Newborn Screening For The Diagnosis of SCID,

NG Y. Y., FIRTINA S., HATIRNAZ N. Ö., KIYKIM A., AYDINER E., ÖZEN A. O., et al.

4. Klinik İmmünoloji Kongresi, Türkiye, 11 - 14 Nisan 2018

“Çıplak” Ağır Kombine İmmün Yetmezlikli 2 Kardeşte Tanımlanan Yeni Foxn1 Mutasyonu

FIRTINA S., ÇİPE F., KIYKIM A., HATIRNAZ N. Ö., SUDUTAN T., AYDOĞMUŞ Ç., et al.

4. Klinik İmmünoloji Kongresi, Türkiye, 11 - 14 Nisan 2018

Hiper IgE hastalarında genişlenfosit alt-tiplendirme DOCK8 ve STAT3 ayrımını gösteren belirteç nedir?

Başer D., ÖĞÜLÜR İ., KIYKIM A., Kasap N., NAİN E., BARIŞ S., et al.

4. Klinik İmmünoloji Kongresi, Antalya, Türkiye, 11 - 14 Nisan 2018

Dedicator of cytokinesis 8 defektif hastalarda grup 3 innate lenfoid hücreleri eksikliği mevcuttur

EKEN A., Okus F. Z., PATIROĞLU T., CANATAN H., BARIŞ S., KARAKÜKCÜ M., et al.

4. klinik immunoloji kongresi, Türkiye, 11 - 14 Nisan 2018

CD55 Deficiency, Early-Onset Protein-Losing Enteropathy and Trombosis

Özen A. O., Comrıe A., Ardy R., Conde D., Dalgıç B., Beşer Ö. F., et al.

World Immune Regulation Meeting XII, Dubendorf, İsviçre, 14 - 17 Mart 2018

STAT1 gain-of-function the immune disregulated mechanisms behind the disease

BARIŞ S., ÖĞÜLÜR İ., CHARBONNIER L. M., ALROQI F., KIYKIM A., AYDINER E., et al.

World Immune Regulation Meeting XII, Davos, İsviçre, 14 - 17 Mart 2018

Akan hücre ölçerde LRBA protein ifadesi tayini ile gerçek LRBA hastaları ayırt edilebilir mi?

ÖĞÜLÜR İ., KIYKIM A., AYDINER E., BARIŞ S., ÖZEN A. O.

XXIV. Ulusal Allerji ve Klinik İmmünoloji Kongresi, Antalya, Türkiye, 18 - 21 Kasım 2017

Hypomorfic JAK3 and IL2RG Mutations Presenting with a Predominantly Antibody DEficiency Phenotype

KIYKIM A., FIRTINA S., ye z., ee n., SAYİTOĞLU M., BARIŞ S., et al.

European Society for Immunodeficiencies (ESID) Meeting, 11 - 14 Kasım 2017

Diagnostics Of Primary Antibody Deficiencies Through Targeted Next Generation Sequencing Panel

NG Y. Y., FIRTINA S., HATIRNAZ N. Ö., camcıoğlu y., AYDINER E., KIYKIM A., et al.

International Primary Immunodeficiencies Congress, 8 - 10 Kasım 2017

Molecular Dıagnosıs Of Scıd Patıents By A Custom Desıgned Targeted Next Generatıon Sequencıng Panel

FIRTINA S., SAYİTOĞLU M., HATIRNAZ N. Ö., KIYKIM A., AYDINER E., BARIŞ S., et al.

International Primary Immunodeficiencies Congress, 8 - 10 Kasım 2017

Dignostics of primary antibody deficiencies through targeted next generation sequencing panel

NG Y. Y., Firtina S., HATIRNAZ NG Ö., Kara M., Somer A., CAMCIOĞLU Y., et al.

IPIC 2017, 8 - 10 Kasım 2017

MOLECULAR DIAGNOSIS OF SCID PATIENTS BY A CUSTOM DESIGNED TARGETED NEXT GENERATION SEQUENCING PANEL

FIRTINA S., SAYİTOĞLU M., NG HATIRNAZ O., KIYKIM A., AYDINER E., BARIŞ S., et al.

ınternational Primary Immunodeficiencies Congress 2017, 8 - 10 Kasım 2017

Diagnostics of Primary Antibody Deficiencies Through Targeted Next Generation Sequencing Panel

NG Y. Y., Fırtına S., HATIRNAZ NG Ö., Kara M., CAMCIOĞLU Y., AYDINER E., et al.

IPIC 2017, 8 - 10 Kasım 2017

Molecular Diagnosis of SCID Patients by a custom designed targeted next generation sequencing panel

Fırtına S., SAYİTOĞLU M., HATIRNAZ NG Ö., Kıykım A., AYDINER E., Barış S., et al.

IPIC 2017, 8 - 10 Kasım 2017

The effect of in vitro high dose vitamin-D on lymphocytes in children with atopic dermatitis

ÖĞÜLÜR İ., ÖZEN A. O., NAİN E., KIYKIM A., BARIŞ S., AYDINER E.

PAAM 2017, 26 - 28 Ekim 2017

The applicability of our product to evaluate the baked milk tolerance in cow’s milk allergic children

KIYKIM A., ÖZEN A. O., GÜNEŞ F. E., NAİN E., ÖĞÜLÜR İ., AKTAÇ Ş., et al.

PAAM 2017, 26 - 28 Ekim 2017

Reference values for lymphocyte subsets in healthy children and adolescent JMF Marmara Center

BESCİ Ö., ÖĞÜLÜR İ., ÇİÇEKKÖKÜ D., KIYKIM A., NAİN E., BORAN P., et al.

18th Biennial Meeting of ESID 2017, 11 - 14 Ekim 2017

TREC/KREC analysis and their clinical correlation an severe combined imune deficiency

HATIRNAZ NG Ö., Fırtına S., SAYİTOĞLU M., nepesov s., Kıykım A., AYDINER E., et al.

IPIC 2017, 8 - 10 Ekim 2017

Progressive mutifocal Leukoencephalopathy in a child with DOCK8 deficiency

SOMER A., torun s., ACAR E. M., aygün e., bektaş g., ÇALIŞKAN M. M., et al.

IPIC 2017, 8 - 10 Ekim 2017

Molecular Diagnosis of SCID patients by a custom designated targeted next generation sequencing panel

Fırtına S., SAYİTOĞLU M., HATIRNAZ NG Ö., Kıykım A., AYDINER E., Baris S., et al.

IPIC 2017, 8 - 10 Ekim 2017

Adverse Reactions to IVIG in primary immune deficiency patients: MArmara experience

Kıykım A., Nain E., ÖZEN A. O., Barış S., AYDINER E.

IPIC 2017, 8 - 10 Ekim 2017

Rapid SCIG infusion in primary immune deficiency patients: Marmara experience

Kıkyım A., Ercan N., ÖZEN A. O., Barış S., AYDINER E.

IPIC 2017, 8 - 10 Ekim 2017

Immunodeficiency caused by activating mutations in the subunits of PI3K and treatment with sirolimus

KIYKIM A., AYDINER E., ÖĞÜLÜR İ., NAİN E., BARIŞ S., ÖZEN A. O.

18th Biennial Meeting of ESID 2017, 11 - 14 Eylül 2017

Hematopoietic stem cell transplantation in patients with heterozygous STAT1 gain of function mutation.

Kıykım A., Charbonnier L., AKÇAY A., Ercan N., AYDINER E., ÖZEN A. O., et al.

ESID 2017, 11 - 14 Eylül 2017

Hypomorphic JAK3 and IL2RG mutations presenting with a predominanty antibody deciency phenotype

Kıykım A., Fırtına S., zhang Y., Ercan N., SAYİTOĞLU M., Baris S., et al.

ESID 2017, 11 - 14 Eylül 2017

The Role of NK Cell Subsets in Ataxia Telangiectasia and Common Variable Immunodeficiency

DENİZ G., GELMEZ M. Y., AKDENİZ N., Özçit G., Kıykım A., AYDINER E., et al.

ISAC 2017, 10 - 14 Haziran 2017

The role of NK Cell Subsets in Ataxia Talengectasia and Common Variable Immunodeficiency

DENİZ G., GELMEZ M. Y., AKDENİZ N., özçit G., Kıykım A., AYDINER E., et al.

ISAC 2017, 10 - 14 Haziran 2017

Immune Deficiency in Patients with Non Cystic Fibrosis Bronchiectasis and Relationship with Clinical Parameters

BEKİR M., OLGUN YILDIZELİ Ş., kocakaya d., ERYÜKSEL S. E., AYDINER E., ÖĞÜLÜR İ., et al.

AMERİCAN THORACİC SOCİETY ANNUAL CONGRESS 2017, 19 - 24 Mayıs 2017

Primer Antikor Yetersizliği Olan Hastalarda Saptanan Bruton Tirozin Kinaz (BTK) Gen Varyasyonları

FIRTINA S., NG Y. Y., HATIRNAZ N. Ö., HASKOLOĞLU Z. Ş., KIYKIM A., AYDINER E., et al.

XXIV. Ulusal İmmünoloji Kongresi, Türkiye, 27 - 30 Nisan 2017

Kalıtsal İnsan CD55 Eksikliği Hastalığı Modelinde T Hücre Eş-uyarımı ve CD55 Sinyalizasyonu

ÖZEN A. O., ÖĞÜLÜR İ., KIYKIM A., BARIŞ S., AYDINER E.

XXIV. Ulusal İmmünoloji Kongresi, İstanbul, Türkiye, 27 - 30 Nisan 2017

Primer Antikor Yetersizliği Olan Hastalarda Saptanan Bruton Kinaz (BTK) Gen Varyasyonları

Fırtına S., Yin Y., HATIRNAZ NG Ö., HASKOLOĞLU Z. Ş., Kıykım A., AYDINER E., et al.

24.Ulusal İmmünoloji Kongresi, Türkiye, 27 - 30 Nisan 2017

Primer İmmünyetersizlik hastalarında NKp30, NKp46, NKG2D, Perforin ve Granzim mRNA ekspresyonu

ÇINAR S., GELMEZ M. Y., AKDENİZ N., Özçit G., Kıykım A., AYDINER E., et al.

XXIV. Ulusal İmmünoloji Kongresi, İstanbul, Türkiye, 27 - 30 Nisan 2017, ss.28

Primer İmmün Yetersizlik Hastalarında NKp30, Nkp46, NKG2D, Perforin ve Granzim mRNA Ekspresyonu

ÇINAR S., GELMEZ M. Y., AKDENİZ N., Özçit G., Kıykım A., AYDINER E., et al.

24. Ulusal İmmünoloji Kongresi, Türkiye, 27 - 30 Nisan 2017

Primer Antikor Yetmezlik Hastalarında Hastalığa Sebep Olan Varyantların Yen Nesil Genetik Tanı Paneli ile Tespiti

Firtina S., NG Y. Y., HATIRNAZ NG Ö., CAMCIOĞLU Y., AYDINER E., Kara M., et al.

3. Klinik İmmünoloji Kongresi, Türkiye, 12 - 15 Nisan 2017

Primer Antikor Yetmezlik Hastalarında Hastalığa Sebep Olan Varyantların Yeni Nesil Genetik Tanı Paneli ile Tespiti

FIRTINA S., NG Y. Y., HATIRNAZ N. Ö., CAMCIOĞLU Y., AYDINER E., kara m., et al.

3. Klinik İmmünoloji Kongresi, Türkiye, 12 - 15 Nisan 2017

Erişkin Yaşta Tanı Alan X’e Bağlı Hipomorfik İmmün Yetmezlik

KIYKIM A., FIRTINA S., NAİM E., BARIŞ S., SAYİTOĞLU M., AYDINER E., et al.

3. Klinik İmmünoloji Kongresi, Türkiye, 12 - 15 Nisan 2017

Ağır Kombine İmmün Yetmezlik Hastalarında TREC/KREC Analizleri ve Klnik Uyumunun Araştırılması

NG Y. Y., Firtina S., HATIRNAZ NG Ö., Nepesov S., Kıykım A., AYDINER E., et al.

3. Klinik İmmünoloji Kongresi, Türkiye, 12 - 15 Nisan 2017

Ağır Kombine İmmün Yetmezlik Hastalarında TREC/KREC Analizleri ve Klinik Uyumun Araştırılması

NG Y. Y., FIRTINA S., HATIRNAZ N. Ö., nepesov s., KIYKIM A., AYDINER E., et al.

3. Klinik İmmünoloji Kongresi, Türkiye, 12 - 15 Nisan 2017

Erişkin Yaşta Tanı Alan X’xxe bağlı Hipomorfik İmmün Yetmezlik

Kıykım A., Fırtına S., Naim E., Barış S., SAYİTOĞLU M., AYDINER E., et al.

3. Klinik İmmünoloji Kongresi, Türkiye, 12 - 15 Nisan 2017

KİSTİK FİBROSİS DIŞI BRONŞEKTAZİ HASTALARINDA YAŞAM KALİTESİ: PSİKOLOJİK DURUM VE HASTALIK ŞİDDETİNİN KONTROLÜ

BEKİR M., OLGUN YILDIZELİ Ş., kocakaya d., ERYÜKSEL S. E., AYDINER E., ÖĞÜLÜR İ., et al.

TÜRK TORAKS DERNEĞİ 20. YILLIK KONGRESİ, Türkiye, 5 - 09 Nisan 2017

Diagnostic Flow Cytometry And Treatment Experience in LRBA Deficiency 4 patients from Marmara

ÖĞÜLÜR İ., Kıykım A., AYDINER E., Barış S., ÖZEN A. O., NAİN E., et al.

ESID 2016 Biennial Meeting, 21 - 24 Eylül 2016

Evaluation of DOCK8 Deficienct Patients A single Center Experience From Turkey

Kıykım A., AYDINER E., ÖĞÜLÜR İ., Barış S., NAİN E., ŞAH O., et al.

ESID 2016 Biannual Meeting, 21 - 24 Eylül 2016

Early onset protein losing enteropathy bowel inflammation and thrombosis in patients with complement regulator deficiency

Ardy R., Özen A. O., Comrie W., Dominguez C., Dalgıç B., Beşer Ö., et al.

ESID 2016 Biennial Meeting, Barcelona, İspanya, 21 - 24 Eylül 2016

Lymphocyte subsets in pediatric common variable immune deficiencies with organ involvement

ÖĞÜLÜR İ., AYDINER E., ÖZEN A. O., kıykım a., NAİN E., çiçekkökü D., et al.

2016 ESID Biennal Meeting, 21 Eylül 2016

Evaluation of DOCK8 deficient patients A single center experience from Turkey

Kıykım A., AYDINER E., ÖĞÜLÜR İ., Barış S., NAİN E., ŞAH O., et al.

2016 ESID Biennal meeting, 21 - 24 Eylül 2016

Neurocognitive Impairement in Ataxia Telangiectasia Patients and Their Parents

UYAR E., AKTÜRK H., Usanmaz S., Kıykım A., Aydıner Ö., Somer A., et al.

2916 ESID Biennal Meeeting, 21 - 24 Eylül 2016

Is there immunodeficiency in heterozygous carrier for ataxia telangiectasia

ÖĞÜLÜR İ., Barış S., ÖZEN A. O., UYAR E., Kıykım A., Çiçekköükü D., et al.

2016 ESID Biennal Meeting, 21 - 24 Eylül 2016

IRAK1 mutation confers susceptibility to autoimmune manifestations

Mehawej C., Massad M., Kıykım A., AYDINER E., Barış S., Chou J., et al.

2016 ESID Biennal Meeting, 21 - 24 Eylül 2016

Identification of genetic variation by targeted next generation sequencing in Turkish SCID patient

Fırtına S., SAYİTOĞLU M., HATIRNAZ NG Ö., Kıykım A., AYDINER E., nepesov s., et al.

2016 ESID Biennal Meeting, 21 - 24 Eylül 2016

Obesity and pediatric psoriasis: Prevalence, impact on disease severity and progression

ERGUN S. A. T., SEÇKİN GENÇOSMANOĞLU D., AYDINER E., SALMAN A., TEKİN B., BÜLBÜL BAŞKAN E., et al.

13th Congress of the European Society for Pediatric Dermatology, 26 - 28 Mayıs 2016 Sürdürülebilir Kalkınma

Obesity and pediatric psoriasiS Prevalance impact on disease severity and progression

ERGUN S. A. T., SEÇKİN GENÇOSMANOĞLU D., AYDINER E., BÜLBÜL BAŞKAN E., ALPSOY E., ONSUN N.

EUROPEAN SOCIETY FOR PEDIATRIC DERMATOLOGY, 26 - 28 Mayıs 2016 Sürdürülebilir Kalkınma

Gastrointestinal tutulumu olan immun yetmezlikli olgularin endoskopik ve histopatolojik değerlendirilmesi

ŞAHİN AKKELLE B., TUTAR E., ÖZTÜRK B., AYDINER E., ERTEM ŞAHİNOĞLU D.

11.Ulusal Çocuk Gastroenteroloji ve Beslenme Kongresi, 2016., 04 Mayıs 2016

Intracellular staining of DOCK8 LRBA SAP and XIAP proteins by flow cyttometry Marmara Experience

ÖĞÜLÜR İ., barış S., ÖZEN A. O., Kıykım A., Bakır M., AYDINER E., et al.

3rd International Molecular Immunology & Immunogenetics Congress, 27 - 30 Nisan 2016

Basophil activation test is reliable for inhalant allergens in pediatric patients

ÖĞÜLÜR İ., Kıykım A., Barış S., ÖZEN A. O., Onat E. G., Bakır M., et al.

3rd International Molecular Immunology & Immunogenetics Congress, 27 - 30 Nisan 2016

Intracellular staining of DOCK8 LRBA SAP and XIAP proteins by flow cytometry Marmara experience

ÖĞÜLÜR İ., Barış S., ÖZEN A. O., Kıykım A., bakır M., AYDINER E., et al.

3rd International Molecular Immunology & Immunogenetics Congress (MIMIC-III), 27 - 30 Nisan 2016

DO CUT OFF VALUES OF IgE AND EOSINOPHIL LEVELS HELP DISCRIMINATE HYPERIGE SYNDROME FROM ATOPIC DISEASES

AYDINER E., Kiykim A., Yuce E., Barış E., NAİN E., KELEŞ S., et al.

2016 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference, 14 - 17 Nisan 2016

Monogenic Primary Immune Deficiencies Identified In a Pediatric Onset CVID Cohort Is there a predictive Marker

AYDINER E., Kiykim A., NAİN E., Kaçmaz M., ÖĞÜLÜR İ., Barış S., et al.

2016 CIS Annual Meeting: Immune Deficiency & Dyregulation North American Conference, 14 - 17 Nisan 2016

A PATIENT WITH A MUTATION IN CD40L PRESENTING WITH PANHYPOGAMMAGLOBULINEMIA AND NATURAL KILLER CELL LYMPHOPENIA

Safa B., AYDINER E., Kıykım A., NAİN E., ÖZEN A. O., bachiloğlu r., et al.

2016 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference, 14 - 17 Nisan 2016

A patient with a mutation in CD40L presenting with panhypogammaglobulinemia and natural killer lymphopenias

Barış S., AYDINER E., kıykım a., NAİN E., ÖZEN A. O., hoyosbachioglu r., et al.

2016 CIS Annual Meeting: Immune Deficiency & Dysregulation North American Conference, 14 - 17 Nisan 2016

DO CUT-OFF VALUES OF IgE AND EOSINOPHIL LEVELS HELP DISCRIMINATE HYPERIGE SYNDROME FROM ATOPIC DISEASES?

Karakoc-Aydiner E., Kiykim A., Yuce E. G., Baris E., Nain E., Keles S., et al.

CIS Annual Meeting on Immune Deficiency and Dysregulation North American Conference, Massachusetts, Amerika Birleşik Devletleri, 14 - 17 Nisan 2016, cilt.36, ss.254

MONOGENIC PRIMARY IMMUNE DEFICIENCIES IDENDIFIED IN A PEDIATRIC-ONSET CVID COHORT, IS THERE A PREDICTIVE MARKER?

Karakoc-Aydiner E., Kiykim A., Nain E., Kacmaz M., Ogulur I., BARIŞ S., et al.

CIS Annual Meeting on Immune Deficiency and Dysregulation North American Conference, Massachusetts, Amerika Birleşik Devletleri, 14 - 17 Nisan 2016, cilt.36, ss.253-254

A PATIENT WITH A MUTATION IN CD40L PRESENTING WITH PANHYPOGAMMAGLOBULINEMIA AND NATURAL KILLER CELL LYMPHOPENIA

BARIŞ S., Karakoc-Aydiner E., Kiykim A., Nain E., Ozen A. O., Hoyos-Bachiloglu R., et al.

CIS Annual Meeting on Immune Deficiency and Dysregulation North American Conference, Massachusetts, Amerika Birleşik Devletleri, 14 - 17 Nisan 2016, cilt.36, ss.311

Ataksi Telenjiektazi heterozigot taşıyıcılarda immün yetmezlik var mı

ÖĞÜLÜR İ., AYDINER E., Barış S., ÖZEN A. O., UYAR E., kıykım a., et al.

3. Marmara Pediatri Kongresi, Türkiye, 18 - 20 Şubat 2016

Gene Therapy Using a Self Inactivating Lentiviral Vector Improves Clinical and Laboratory Manifestations of Wiskott Aldrich Syndrome

Julia I., JH H., Armant M., Francis M., Danceraneu C., Brenda M. K., et al.

ASH 57th Annual Meeting and Exposition, 5 - 08 Aralık 2015