E. Karakoc‐Aydiner

发表

Impaired respiratory burst contributes to infections in PKCδ-deficient patients

J. Casanova, L. Abel, G. Uzel, 2021, The Journal of experimental medicine.

Notch1-CD22-Dependent Immune Dysregulation in the SARS-CoV2-Associated Multisystem Inflammatory Syndrome in Children

A. Randolph, R. Geha, E. Crestani, 2022, Research square.

Diagnostic modalities based on flow cytometry for chronic granulomatous disease: a multicenter study in a well-defined cohort.

S. Barış, Y. Camcıoğlu, G. Yeşil, 2020, The journal of allergy and clinical immunology. In practice.

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

J. Hughes, J. McElwee, Y. Zhang, 2015, Science.

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

I. Barlan, S. Barış, E. Karakoc‐Aydiner, 2015, Journal of Clinical Immunology.

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

C. Klein, A. Franke, H. von Bernuth, 2017, Inflammatory bowel diseases.

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

İ. Reisli, T. Chatila, A. Al-Shaibi, 2019, The journal of allergy and clinical immunology. In practice.

Parents of ataxia‐telangiectasia patients display a distinct cellular immune phenotype mimicking ATM‐mutated patients

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

Early-onset neurolupus: A challenge for pediatricians

I. Barlan, S. Barış, N. Yıldız, 2015 .

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

T. Ergun, E. Alpsoy, E. Karakoc‐Aydiner, 2017, The Australasian journal of dermatology.

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

S. Barış, E. Karakoc‐Aydiner, G. Gokcay, 2021, Allergologia et immunopathologia.

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

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

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

S. Tangye, O. Sanal, I. Tezcan, 2021, Journal of Clinical Immunology.

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

Andrew J. Oler, S. Choo, S. Tangye, 2020, Blood.

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.

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.

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

I. Barlan, S. Barış, C. Ozdemir, 2011, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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.

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.

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

A. Eifan, I. Barlan, S. Barış, 2015, Journal of investigational allergology & clinical immunology.

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

I. Barlan, S. Barış, H. Alpay, 2016, European Journal of Pediatrics.

House Dust Mites Confer a Distinct Immunological Feature among Dermatitis.

I. Barlan, S. Barış, G. Demirel, 2016, Iranian journal of allergy, asthma, and immunology.

Defects Along the Th17 Differentiation Pathway Underlie Genetically Distinct Forms of the Hyper IgE Syndrome

İ. Reisli, T. Chatila, A. Somer, 2010 .

PRACTITIONER ’ S CORNER Inhaled 1-Antitrypsin Administered to Treat Pneumatocele in Autosomal Dominant Hyperimmunoglobulin E Syndrome

T. Chatila, I. Barlan, S. Barış, 2013 .

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.

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

T. Chatila, M. Gursel, S. Barış, 2021, Journal of clinical 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.

Efficacy of intravenous immunoglobulin treatment in children with common variable immunodeficiency.

S. Barış, E. Karakoc‐Aydiner, H. Ercan, 2011, Journal of investigational allergology & clinical immunology.

A Patient with Novel ICOS Mutation Presented with Progressive Loss of B Cells

S. Barış, L. Charbonnier, E. Karakoc‐Aydiner, 2020, Journal of clinical immunology.

Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome

R. Pfundt, R. Louie, K. Girisha, 2022, bioRxiv.

Therapeutic options for CTLA-4 Insufficiency.

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

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

D. Caimmi, J. Caubet, P. Rodríguez Del Río, 2021, Allergy.

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

J. Franco, Y. Lau, O. Sanal, 2017, Front. Immunol..

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.

Inhaled alpha1-antitrypsin administered to treat pneumatocele in autosomal dominant hyperimmunoglobulin E syndrome.

T. Chatila, I. Barlan, S. Barış, 2013, Journal of investigational allergology & clinical immunology.

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

I. Barlan, T. Akkoç, E. Karakoc‐Aydiner, 2011, The Journal of allergy and 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 .

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

B. Lambrecht, A. Fischer, E. López-Granados, 2020, Journal of Allergy and Clinical Immunology.

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

S. Barış, E. Karakoc‐Aydiner, A. Ozen, 2021, Journal of Clinical Immunology.

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.

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

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

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

Edward R B McCabe, Bodo Grimbacher, Christoph Klein, 2009, The Journal of allergy and clinical immunology.

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

T. Chatila, M. Yılmaz, A. Somer, 2009, The Journal of allergy and clinical immunology.

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

T. Chatila, S. Holland, C. Klein, 2009, The Journal of allergy and clinical immunology.

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

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

Clinical and Laboratory Factors Affecting the Prognosis of Severe Combined Immunodeficiency

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

Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory disease

Andrew J. Oler, I. Vujkovic-Cvijin, Y. Belkaid, 2021, Nature 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.

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.

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.

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

R. Geha, A. Bousfiha, W. Al-Herz, 2021, Journal of Clinical Immunology.

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

Thomas E. Hughes, H. Kong, A. Freeman, 2017, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Immune system defects in DiGeorge syndrome and association with clinical course

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

Immune deficiencies , infection , and systemic immune disorders Defects along the TH 17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

T. Chatila, M. Yılmaz, A. Somer, 2009 .

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.

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

S. Barış, E. Karakoc‐Aydiner, V. Zimmermann, 2022, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

R. Geha, J. Chou, W. Al-Herz, 2022, Clinical immunology.

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.

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

I. Barlan, S. Barış, E. Karakoc‐Aydiner, 2014, Journal of investigational allergology & clinical immunology.

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

I. Vujkovic-Cvijin, Y. Belkaid, R. Apps, 2020, Nature Immunology.

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

T. Chatila, M. Gursel, S. Barış, 2021, Journal of Clinical Immunology.

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

A. Gennery, A. Worth, L. Hammarström, 2019, The Journal of allergy and clinical immunology.

Outcome of hypogammaglobulinemia in children: immunoglobulin levels as predictors.

I. Barlan, S. Barış, C. Ozdemir, 2010, Clinical immunology.

GIMAP5 maintains liver endothelial cell homeostasis and prevents portal hypertension

D. Jain, R. Lifton, D. Kleiner, 2021, The Journal of experimental medicine.

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.

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

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

A Patient with Novel ICOS Mutation Presented with Progressive Loss of B Cells

S. Barış, L. Charbonnier, E. Karakoc‐Aydiner, 2020, 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.

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

A. Koc, I. Barlan, Selin Yıldırım, 2021, Minerva pediatrica.

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

T. Akçay, E. Adal, F. Dede, 2012, European journal of endocrinology.

Osteoporosis: An ignored complication of CVID

I. Barlan, S. Barış, C. Ozdemir, 2011, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

T. Chatila, E. Karaca, M. Ozen, 2013, Gene.

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

I. Barlan, S. Barış, C. Ozdemir, 2011 .

Homozygous IL37 mutation associated with infantile inflammatory bowel disease

Kenneth G. C. Smith, M. Lenardo, H. Su, 2021, Proceedings of the National Academy of Sciences.

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

I. Barlan, S. Barış, Ahmet Özen, 2016, Balkan medical journal.

Severe Allergic Dysregulation Due to A Gain of Function Mutation in the Transcription Factor STAT6.

T. Chatila, M. Massaad, Mehdi Benamar, 2023, The Journal of allergy and clinical immunology.

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.

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

A. Eifan, I. Barlan, M. Akın, 2010, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and 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.

Lymphocyte Subset Abnormalities in Pediatric-Onset Common Variable Immunodeficiency

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

Socialization During the COVID-19 Pandemic: The Role of Social and Scientific Networks During Social Distancing.

R. Kelishadi, L. Uddin, M. Khafaie, 2021, Advances in experimental medicine and biology.

COVID-19 disease characteristics in different pediatric age groups.

B. Karadag, E. Karakoc‐Aydiner, M. Aydın, 2022, Journal of infection in developing countries.

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.

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.

Efficacy of intravenous immunoglobulin treatment in children with common variable immunodeficiency.

S. Barış, C. Ozdemir, E. Karakoc‐Aydiner, 2011, Journal of investigational allergology & clinical immunology.

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.

Activated Phosphoinositide 3-Kinase δ Syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.

A. Schulz, V. Lougaris, A. Plebani, 2023, 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 .

Skin Abscesses, Eczema and Lymphopenia

E. Karakoc‐Aydiner, A. Ozen, 2019, Pediatric Immunology.

Evaluation of Clinical and Immunological Alterations Associated with ICF Syndrome.

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

Chronic Diarrhea, Recurrent Edema and Respiratory Infections

E. Karakoc‐Aydiner, D. Ertem, A. Ozen, 2019, Pediatric Immunology.

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome (vol 124, pg 1289, 2009)

T. Chatila, J. Puck, S. Ehl, 2010 .

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

R. Pfundt, R. Louie, K. Girisha, 2024, Nature communications.

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.