S. Barış

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

A regulatory T cell Notch4-GDF15 axis licenses tissue inflammation in asthma

R. Geha, E. Crestani, T. Chatila, 2020, Nature Immunology.

Early-onset neurolupus: A challenge for pediatricians

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

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.

Predictors of atopic dermatitis phenotypes and severity: roles of serum immunoglobulins and filaggrin gene mutation R501X.

S. Barış, H. Ercan, D. Kıraç, 2013, 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.

A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity

D. Chaussabel, J. Casanova, P. Li, 2018, Science 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.

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.

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.

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.

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.

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

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

House Dust Mites Confer a Distinct Immunological Feature among Dermatitis.

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

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

S. Barış, 2015 .

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

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

Comprehensive comparison between 222 CTLA‐4 haploinsufficiency and 212 LRBA deficiency patients: a systematic review

S. Barış, Niusha Sharifinejad, M. Zaki-Dizaji, 2021, Clinical and experimental immunology.

ASSOCIATION BETWEEN GENETIC POLYMORPHISM IN DNA REPAIR GENES AND RISK OF B-CELL LYMPHOMA

T. Celkan, M. Güven, B. Batar, 2009, Pediatric hematology and oncology.

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.

All together to Fight Novel Coronavirus Disease (COVID-19).

L. Uddin, M. Perc, W. Al-Herz, 2020, The American journal of tropical medicine and hygiene.

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.

Primary Immune Regulatory Disorders and Targeted Therapies.

S. Barış, Burcu Kolukisa, 2021, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Characterization of the clinical and immunological phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.

William J. Astle, Sri V. V. Deevi, Kenneth G. C. Smith, 2020, The Journal of allergy and clinical immunology.

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.

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

S. Barış, E. Nain, A. Kıykım, 2018 .

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.

Is house dust mite spesific sublingual immunotherapy successful in termination of inhaled corticosteroid treatment in children with asthma

S. Barış, C. Ozdemir, E. Aydıner, 2018 .

Clinical variability of asphyxiating thoracic dystrophy (Jeune) syndrome: Evaluation and classification of 13 patients

B. Tüysüz, S. Barış, R. Madazlı, 2009, American journal of medical genetics. Part A.

Long Term Follow-up of Hyperimmunoglobulin M Syndrome Cases

G. Deniz, I. Barlan, S. Barış, 2010 .

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.

Immune alterations in subacute sclerosing panencephalitis reflect an incompetent response to eliminate the measles virus

C. Gurses, S. Barış, G. Saruhan-Direskeneli, 2021, PloS one.

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..

Atypical presentation of Takayasu’s arteritis in an adolescent

H. Direskeneli, I. Barlan, S. Barış, 2015 .

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

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

A patient with mushroom allergy; a new etiological agent of Kounis syndrome.

S. Barış, C. Karabay, Fatma Merve Tepetam, 2016, Tuberkuloz ve toraks.

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.

Experience with intravenous immunoglobulin in severe childhood atopic dermatitis.

S. Barış, A. Ozen, Elif Karakoç Aydıner, 2012, Allergologia et immunopathologia.

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 .

Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness.

A. Aydın, T. Celkan, H. Onal, 2009, The Turkish journal of pediatrics.

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.

Sinus pericranii: Diagnosis with contrast enhanced MRI venography

S. Barış, S. Albayram, Isa Ozyilmaz, 2015 .

Granzyme B Gene Polymorphism Associated with Subacute Sclerosing Panencephalitis

C. Gurses, S. Barış, A. Gokyigit, 2014, Neuropediatrics.

Immune dysfunction in inborn errors of immunity causing malignancies

S. Barış, Burcu Kolukisa, 2021, Expert review 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.

Mucus sialylation determines intestinal host-commensal homeostasis

A. Griffiths, N. Warner, C. Bertozzi, 2022, Cell.

A scoring system predicting the clinical course of CLPB defect based on the foetal and neonatal presentation of 31 patients

C. Saunders, S. Rahman, S. Wortmann, 2017, Journal of Inherited Metabolic Disease.

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.

Congenital iRHOM2 deficiency causes ADAM17 dysfunction and environmentally directed immunodysregulatory disease

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

Outcome of Hematopoietic Stem Cell Gene Therapy for Wiskott-Aldrich Syndrome

Julia T. Chu, David A. Williams, F. Bushman, 2019, Blood.

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.

A regulatory T cell Notch4–GDF15 axis licenses tissue inflammation in asthma

R. Geha, E. Crestani, T. Chatila, 2020, Nature Immunology.

DNA repair gene XPD and XRCC1 polymorphisms and the risk of febrile neutropenia and mucositis in children with leukemia and lymphoma.

T. Celkan, M. Güven, B. Batar, 2012, Leukemia research.

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.

A Novel ATM Gene Mutation Affecting Splicing in an Ataxia-Telangiectasia Patient

S. Barış, S. B. Eltan, Esra Arslan Ateş, 2021, Molecular Syndromology.

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.

Hematopoietic stem cell transplantation in CD40 ligand deficiency: A single-center experience.

S. Barış, F. Çelmeli, Ahmet Özen, 2020, Pediatric transplantation.

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.

Dock8 Functions as an Adaptor That Links Toll-like Receptor– Myd88 Signaling to B Cell Activation Hhs Public Access

Alessandro Plebani, Rima Wakim, Kate Fitzgerald, 2022 .

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

I. Barlan, S. Barış, T. Akkoç, 2011 .

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.

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.

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.

Comparison of Color Doppler US and CT Portography in Evaluating Portal Hypertension in Children

I. Adaletli, S. Barış, S. Kuruğoğlu, 2012, Southern medical journal.

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.

Acquired origin of the left anterior descending coronary artery from the pulmonary artery: A complication of the arterial switch operation

S. Barış, Isa Ozyilmaz, A. Eroğlu, 2011, Annals of pediatric cardiology.

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.

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.

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.

Treatment of Pediatric Burkitt Lymphoma in Turkey

A. Ozkan, T. Celkan, I. Adaletli, 2010, Journal of pediatric hematology/oncology.

Nijmegen-Breakage Syndrome; Two Siblings Presenting with Different Phenotypes

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

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

S. Barış, E. Nain, A. Kıykım, 2017 .

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

I. Tezcan, D. Uçkan, S. Barış, 2017, Pediatric blood & cancer.

Two Chronic Granulomatous Disease Diagnosed in Adult Age.

S. Barış, F. Akyil, T. Sevim, 2016, Turkish thoracic journal.

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.

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

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

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 .

Evaluation of Hyperimmunoglobulin M Syndrome by Flow Cytometry

G. Deniz, I. Barlan, S. Barış, 2015 .

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

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

Acute Promyelocytic Leukemia Treated With Idarubicin Complicated by Focal Segmental Glomerulosclerosis

N. Özdemir, T. Celkan, S. Barış, 2010, Journal of pediatric hematology/oncology.

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

O. Sanal, I. Tezcan, M. Hershfield, 2018, Journal of Clinical Immunology.

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.

Chronic granulomatous disease: is it always associated with infections?

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

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

K. Schwarz, S. Ehl, I. Schulze, 2014, Journal of Clinical Immunology.

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.

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

K. Schwarz, S. Ehl, I. Schulze, 2014, Journal of Clinical Immunology.

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.

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.

Role of glutathione S-transferase M1, T1 and P1 gene polymorphisms in childhood acute lymphoblastic leukemia susceptibility in a Turkish population

T. Celkan, B. Batar, S. Barış, 2015, Meta gene.

Lymphocyte Subset Abnormalities in Pediatric-Onset Common Variable Immunodeficiency

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

Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes

Muhammad Obaidur Rahman, Lindsey B. Rosen, D. Babovic‐Vuksanovic, 2023, iScience.

Author Correction: A regulatory T cell Notch4–GDF15 axis licenses tissue inflammation in asthma

R. Geha, E. Crestani, T. Chatila, 2020, 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.

Intractable atrial flutter presented with severe bradycardia in an infant.

S. Barış, Isa Ozyilmaz, A. Güzeltaş, 2009, Anadolu kardiyoloji dergisi : AKD = the Anatolian journal of cardiology.

A rare cause of ischemic stroke: fibromuscular dysplasia

T. Celkan, S. Barış, S. Albayram, 2009, Neurological Sciences.

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.

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.

Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1.

H. Canatan, A. Eken, S. Barış, 2023, 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.

Investigation of Sleep Quality and Sleep Disorders in Students of Medicine

J. E. Hansen, R. Casaburi, A. Malhotra, 2016 .

Human immunodeficiency reveals GIMAP5 as lymphocyte-specific regulator of senescence

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

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.

Author Correction: A regulatory T cell Notch4–GDF15 axis licenses tissue inflammation in asthma

R. Geha, E. Crestani, T. Chatila, 2021, Nature 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 .

Primary Immun Deficiency in Patients with Non-Cystic Fibrosis Bronchiectasis and Its Relationship with Clinical Parameters.

E. Eryüksel, S. Barış, B. Ceyhan, 2020, Turkish thoracic journal.

Renovascular hypertension in a child with Marfan syndrome.

F. Numan, M. Cantaşdemir, S. Barış, 2010, Anadolu kardiyoloji dergisi : AKD = the Anatolian journal of cardiology.

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

O. Sanal, I. Tezcan, M. Hershfield, 2018, Journal of Clinical Immunology.

DOCK8 functions as an adaptor that links Toll-like receptor–MyD88 signaling to B cell activation

Douglas R. McDonald, L. Notarangelo, A. Plebani, 2012, Nature Immunology.

Evaluation of Clinical and Immunological Alterations Associated with ICF Syndrome.

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

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.

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.