A. Kıykım

A. Somer, S. Barış, M. Muftuoglu, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

M. Haimel, L. Cinel, I. Gursel, 2022, Journal of Clinical Immunology.

Lymphoma Predisposing Gene in an Extended Family: CD70 Signaling Defect

R. Kebudi, A. Kıykım, Aysenur Kaya, 2020, Journal of Clinical Immunology.

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

T. Chatila, D. Krappmann, N. Rezaei, 2022, Journal of Clinical Immunology.

Two patients with chronic mucocutaneous candidiasis caused by TRAF3IP2 deficiency.

M. Lenardo, S. Barış, G. Yeşil, 2020, The Journal of allergy and clinical immunology.

Exaggerated follicular helper T‐cell responses in patients with LRBA deficiency caused by failure of CTLA4‐mediated regulation

R. Geha, J. Chou, T. Chatila, 2017, The Journal of allergy and clinical immunology.

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

F. Rieux-Laucat, A. Schulz, H. Kanegane, 2017, The Journal of allergy and clinical immunology.

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

S. Barış, E. Nain, Ahmet Özen, 2016, Turk pediatri arsivi.

Immunization practices in children with a history of allergies

S. Barış, Ahmet Özen, A. Kıykım, 2020, Turk pediatri arsivi.

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

I. Barlan, S. Barış, E. Karakoc‐Aydiner, 2015, Respiratory medicine.

Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia

J. Casanova, R. Lifton, M. Zatz, 2022, The Journal of experimental medicine.

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

I. Barlan, S. Barış, E. Karakoc‐Aydiner, 2014, Allergy.

Genetic Characteristics, Infectious, and Noninfectious Manifestations of 32 Patients with Chronic Granulomatous Disease

T. Kuijpers, M. de Boer, D. Roos, 2020, International Archives of Allergy and Immunology.

A Stk4-Foxp3–NF-κB p65 transcriptional complex promotes Treg cell activation and homeostasis

T. Chatila, C. Angelini, Mehdi Benamar, 2022, Science Immunology.

A Case Report with a Considerably Delayed Diagnosis of Immunodeficiency: Good's Syndrome

E. Nain, A. Kıykım, F. Akyil, 2017 .

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

G. Mumcu, H. Direskeneli, S. Barış, 2017, International Archives of Allergy and Immunology.

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

İ. Reisli, A. Yildiran, S. Barış, 2022, Allergy.

Effects of Vitamin D on House Dust Mite Sensitized Children with Atopic Dermatitis

S. Barış, E. Nain, A. Kıykım, 2018 .

Therapeutic options for CTLA-4 Insufficiency.

V. Lougaris, T. Morio, K. Sullivan, 2021, The Journal of allergy and clinical immunology.

The Notch1/CD22 signaling axis disrupts Treg function in SARS-CoV-2–associated multisystem inflammatory syndrome in children

A. Randolph, R. Geha, J. Chou, 2022, The Journal of clinical investigation.

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

T. Hirschmugl, I. Barlan, S. Barış, 2015, Journal of Clinical Immunology.

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

A. Fischer, C. Picard, P. Soler-Palacín, 2018, Front. Immunol..

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

M. Hershfield, E. Kıykım, I. Barlan, 2016 .

Biotinidase deficiency mimicking primary immune deficiencies

E. Kıykım, A. Kıykım, M. Cansever, 2015, BMJ Case Reports.

Immediate adverse reactions to intravenous immunoglobulin in primary immune deficiencies: a single center experience.

S. Barış, E. Nain, Ahmet Özen, 2020, The Turkish journal of pediatrics.

The Evaluation of Our Patients with Chronic Granulomatous Disease

I. Barlan, S. Barış, A. Kıykım, 2014 .

Altered Immune Response in Organic Acidemia.

B. Topçu, E. Kıykım, A. Kıykım, 2021, Pediatrics international : official journal of the Japan Pediatric Society.

Primary antibody deficiencies in Turkey: molecular and clinical aspects

U. Ozbek, S. Barış, Y. Camcıoğlu, 2021, Immunologic Research.

Initial presenting manifestations in 16,486 patients with Inborn Errors of Immunity include infections and non-infectious manifestations.

Nurit Assia Batzir, K. Schwarz, D. Foell, 2021, The Journal of allergy and clinical immunology.

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

T. Chatila, I. Barlan, S. Barış, 2016, Journal of Clinical Immunology.

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

S. Barış, N. Kutukculer, C. Aytekin, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

A. Koc, A. Somer, S. Barış, 2019, Pediatric blood & cancer.

Primary Immunodeficiency and Cancer in Children; A Review of the Literature

R. Kebudi, A. Kıykım, M. Şahin, 2019, Current pediatric reviews.

CPR-Content 15-4

R. Kebudi, A. Kıykım, M. Şahin, 2019 .

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

T. Chatila, H. Su, G. Baysoy, 2021, Allergy.

Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2

G. Driessen, L. Daxinger, S. M. van der Maarel, 2017, Clinical genetics.

Clinical and Laboratory Factors Affecting the Prognosis of Severe Combined Immunodeficiency

S. Barış, E. Nain, E. Karakoc‐Aydiner, 2022, Journal of Clinical Immunology.

Natural history and genetic spectrum of the Turkish metaphyseal dysplasia cohort, including rare types caused by biallelic COL10A1, COL2A1, and LBR variants.

B. Tüysüz, H. Apak, A. Kıykım, 2022, Bone.

Polymerase δ deficiency causes syndromic immunodeficiency with replicative stress.

G. Superti-Furga, M. van der Burg, W. Pickl, 2019, The Journal of clinical investigation.

Proven Food-Induced Acute Urticaria and Predictive Factors for Definitive Diagnosis in Childhood

Ç. Aydoğmuş, F. Orhan, O. Cavkaytar, 2021, International Archives of Allergy and Immunology.

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

S. Barış, C. Saçkesen, D. Yazici, 2018, International Archives of Allergy and Immunology.

Notch4 signaling limits regulatory T-cell-mediated tissue repair and promotes severe lung inflammation in viral infections

E. Crestani, T. Chatila, Xu G. Yu, 2021, Immunity.

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

S. Barış, E. Karakoc‐Aydiner, A. Kıykım, 2017, International journal of pediatric otorhinolaryngology.

CD55 Deficiency, Early‐Onset Protein‐Losing Enteropathy, and Thrombosis

J. McElwee, S. Pittaluga, L. Folio, 2017, The New England journal of medicine.

Clinical, Genetic, and Outcome Characteristics of Pediatric Patients with Primary Hemophagocytic Lymphohistiocytosis

M. Elli, Y. Yaman, A. Kıykım, 2022, Turkish archives of pediatrics.

Mutational landscape of severe combined immunodeficiency patients from Turkey

Ozden Hatirnaz Ng, U. Ozbek, S. Barış, 2020, International journal of immunogenetics.

Immune system defects in DiGeorge syndrome and association with clinical course

S. Barış, E. Nain, E. Karakoc‐Aydiner, 2019, Scandinavian journal of immunology.

G6PC3 Deficiency: Primary Immune Deficiency Beyond Just Neutropenia.

I. Barlan, S. Barış, K. Boztug, 2015, Journal of pediatric hematology/oncology.

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

L. Notarangelo, J. Walter, R. Geha, 2019, The journal of allergy and clinical immunology. In practice.

Use of subcutaneous immunoglobulin in primary immune deficiencies.

I. Barlan, S. Barış, Ahmet Özen, 2016, Turk pediatri arsivi.

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

E. Kıykım, S. Barış, K. Boztug, 2016, Clinical immunology.

LRBA deficiency: a rare cause of type 1 diabetes, colitis, and severe immunodeficiency

S. Poyrazoglu, F. Baş, F. Darendeliler, 2020, Hormones.

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

T. Chatila, I. Barlan, S. Barış, 2016, Journal of Clinical Immunology.

Oral Moniliasis and Failure to Thrive

S. Barış, A. Kıykım, 2019, Pediatric Immunology.

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

T. Chatila, S. Barış, L. Charbonnier, 2018, Journal of Clinical Immunology.

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

S. Barış, A. Bereket, S. Turan, 2020, Hormone Research in Paediatrics.

Chronic Rhinosinusitis in Patients with Primary Immunodeficiency

A. Kıykım, Sezin Aydemir, H. Çokuğraş, 2022, International Archives of Allergy and Immunology.

Humoral and cellular immune response to SARS-CoV-2 mRNA BNT162b2 vaccine in pediatric kidney transplant recipients compared with dialysis patients and healthy children

A. Nayır, B. Kocazeybek, N. Yıldız, 2022, Pediatric nephrology.

Nijmegen-Breakage Syndrome; Two Siblings Presenting with Different Phenotypes

M. Tekin, G. Bademci, I. Barlan, 2016 .

A rare cause of severe superficial herpetic skin infection in a 13-month-old female patient: Autosomal recessive HIES -

E. Topal, A. Kıykım, M. Demirtaş, 2018 .

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

S. Barış, E. Nain, A. Kıykım, 2017 .

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

S. Barış, H. Artaç, F. Orhan, 2021, Allergy.

Food-induced anaphylaxis in early childhood and factors associated with its severity.

Ç. Aydoğmuş, F. Orhan, H. Yüksel, 2021, Allergy and asthma proceedings.

Primary antibody deficiencies in Turkey: molecular and clinical aspects

U. Ozbek, S. Barış, Y. Camcıoğlu, 2021, Immunologic Research.

Protein Expression in the Diagnosis of LRBA Deficiency by Flow Cytometer

A. Somer, S. Barış, Ayla Güven, 2018 .

Serving Healthy (?) Food on Toxic Plates

A. Kıykım, 2023, Turkish archives of pediatrics.

Chronic granulomatous disease: is it always associated with infections?

I. Barlan, S. Barış, A. Kıykım, 2012 .

Epithelial Barrier Hypothesis and Its Comparison with the Hygiene Hypothesis

C. Akdis, M. Akdiş, D. Yazici, 2023, Turkish archives of pediatrics.

Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency

J. Casanova, A. Bousfiha, S. Ehl, 2022, The Journal of experimental medicine.

Primary immunodeficiencies: HSCT experiences of a single center in Turkey

C. Bozkurt, Ç. Aydoğmuş, S. Aydoğdu, 2021, Pediatric transplantation.

Functions of NK and iNKT cells in pediatric and adult CVID, Ataxia Telangiectasia and Agammaglobulinemia Patients.

G. Deniz, I. Barlan, E. Karakoc‐Aydiner, 2021, Immunology letters.

Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants

N. Kutukculer, G. Aksu, Ç. Aydoğmuş, 2022, Scandinavian journal of immunology.

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

S. Barış, U. Özbek, Y. Camcıoğlu, 2021, Scandinavian journal of immunology.

Successful Rapid Desensitization of a Pediatric Multiple Sclerosis Patient with Anaphylaxis to Ocrelizumab

Hatice Karaaslan, A. Kıykım, Sezin Aydemir, 2022, Annals of Indian Academy of Neurology.

Lymphocyte Subset Abnormalities in Pediatric-Onset Common Variable Immunodeficiency

S. Barış, E. Karakoc‐Aydiner, A. Kıykım, 2020, International Archives of Allergy and Immunology.

Lymphoma Predisposing Gene in an Extended Family: CD70 Signaling Defect

R. Kebudi, A. Kıykım, Aysenur Kaya, 2020, Journal of Clinical Immunology.

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

S. Barış, Ç. Aydoğmuş, A. Kıykım, 2019, Journal of Clinical Immunology.

Omalizumab may facilitate drug desensitization in patients failing standard protocols

A. Kıykım, N. Canpolat, H. Çokuğraş, 2022, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

J. Casanova, A. Bousfiha, B. Fevang, 2022, The Journal of experimental medicine.

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

David A. Williams, F. Bushman, L. Notarangelo, 2015 .

Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency

G. Baysoy, S. Barış, A. Islek, 2021, Journal of Clinical Immunology.

Profile of the patients who present to immunology outpatient clinics because of frequent infections.

Y. Camcıoğlu, A. Kıykım, N. Akçakaya, 2014, Turk pediatri arsivi.

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

T. Hirschmugl, I. Barlan, S. Barış, 2015, Journal of Clinical Immunology.

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

R. Geha, A. Bousfiha, W. Al-Herz, 2022, The journal of allergy and clinical immunology. In practice.

Immune Reconstitution Inflammatory Syndrome After Hematopoietic Stem Cell Transplantation in a FOXN1-deficient Patient

A. Kıykım, Pinar Onal, S. Nepesov, 2023, Journal of pediatric hematology/oncology.

[Analysis of IFN-γR1 (CD119) and IL-12Rβ1 (CD212) Deficiency by Flow Cytometry].

G. Deniz, N. Hatipoğlu, A. Kıykım, 2023, Mikrobiyoloji bulteni.

Human immunodeficiency reveals GIMAP5 as lymphocyte-specific regulator of senescence

R. Lifton, M. Lenardo, H. Su, 2021, bioRxiv.

Comparison of mitogen-induced proliferation in child and adult healthy groups by flow cytometry revealed similarities

G. Deniz, Y. Camcıoğlu, A. Kıykım, 2022, Immunologic Research.

Monogenic Early-Onset Lymphoproliferation and Autoimmunity: The Natural History of STAT3 GOF Syndrome.

K. Schwarz, M. Weinrich, F. Rieux-Laucat, 2022, The Journal of allergy and clinical immunology.

Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients.

L. Notarangelo, A. Worth, M. Bosticardo, 2023, Clinical immunology.

The Notch1/CD22 signaling axis disrupts Treg function in SARS-CoV-2–associated multisystem inflammatory syndrome in children

A. Randolph, R. Geha, E. Crestani, 2023 .

Evaluation of Clinical and Immunological Alterations Associated with ICF Syndrome.

S. Barış, E. Karakoc‐Aydiner, A. Kıykım, 2023, Journal of clinical immunology.

Polymerase δ deficiency causes syndromic immunodeficiency with replicative stress.

G. Superti-Furga, M. van der Burg, W. Pickl, 2019, The Journal of clinical investigation.

GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway

R. Lifton, I. Tezcan, D. Schwefel, 2024, Nature immunology.

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

S. Barış, Ç. Aydoğmuş, A. Kıykım, 2019, Journal of Clinical Immunology.

Insights into Patient Experiences with Facilitated Subcutaneous Immunoglobulin Therapy in Primary Immune Deficiency: A Prospective Observational Cohort

S. Barış, E. Karakoc‐Aydiner, A. Kıykım, 2024, Journal of clinical immunology.

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

I. Tezcan, S. Barış, A. Ikinciogullari, 2024, Journal of clinical immunology.

Allergen-specific B cell responses in oral immunotherapy-induced desensitization, remission, and natural outgrowth in cow's milk allergy.

C. Akdis, M. Akdiş, M. Sokolowska, 2024, Allergy.

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

L. Notarangelo, J. Walter, R. Geha, 2019, The journal of allergy and clinical immunology. In practice.

Artemis deficiency: A large cohort including a novel variant with increased radiosensitivity

S. Barış, E. Karakoc‐Aydiner, A. Kıykım, 2024, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.