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Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis

Journal of clinical immunology, 2021, Vol.41 (1), p.59-65

2021

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

Journal of clinical immunology, 2016-10, Vol.36 (7), p.641-648

2016

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

Journal of clinical immunology, 2022-04, Vol.42 (3), p.634-652

2022

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Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency

Journal of clinical immunology, 2021-08, Vol.41 (6), p.1406-1410

2021

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Lymphoma Predisposing Gene in an Extended Family: CD70 Signaling Defect

Journal of clinical immunology, 2020-08, Vol.40 (6), p.883-892

2020

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Primary antibody deficiencies in Turkey: molecular and clinical aspects

Immunologic research, 2022-02, Vol.70 (1), p.44-55

2022

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

Journal of clinical immunology, 2022-04, Vol.42 (3), p.582-596

2022

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Correction to: Primary antibody deficiencies in Turkey: molecular and clinical aspects

Immunologic research, 2022-02, Vol.70 (1), p.134-134

2022

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Successful rapid desensitization of a pediatric multiple sclerosis patient with anaphylaxis to ocrelizumab

Annals of the Indian Academy of Neurology, 2022-11, Vol.25 (6), p.1210-1213

2022

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

International journal of pediatric otorhinolaryngology, 2017-06, Vol.97, p.197-201

2017

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Exaggerated T Follicular Helper Cell Responses in LRBA Deficiency Due to Failure of CTLA4-Mediated Regulation

Journal of allergy and clinical immunology, 2017-06, Vol.141 (3), p.1050-1059.e10

2017

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

Respiratory medicine, 2015-09, Vol.109 (9), p.1120-1125

2015

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

Clinical & experimental neuroimmunology, 2016-02, Vol.7 (1), p.79-82

2016

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Serving Healthy (?) Food on Toxic Plates

Turkish archives of pediatrics, 2023-01, Vol.58 (1), p.1-2

Kıykım, Ayça

2023

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Lymphocyte Subset Abnormalities in Pediatric-Onset Common Variable Immunodeficiency

International archives of allergy and immunology, 2020-02, Vol.181 (3), p.228-237

2020

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Chronic Rhinosinusitis in Patients with Primary Immunodeficiency

International archives of allergy and immunology, 2023-03, Vol.184 (3), p.302-310

2023

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

Immunologic research, 2023-02, Vol.71 (1), p.51-59

2023

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

Journal of allergy and clinical immunology, 2018-03, Vol.141 (3), p.1050-1059.e10

2018

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

Turkish journal of medical sciences, 2021-08, Vol.51 (4), p.1814-1824

2021

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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

Frontiers in immunology, 2018-03, Vol.9, p.543-543

2018

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

The New England journal of medicine, 2017-07, Vol.377 (1), p.52-61

2017

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

Scandinavian journal of immunology, 2022-06, Vol.95 (6), p.e13163-n/a

2022

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

Journal of clinical immunology, 2019-01, Vol.39 (1), p.37-44

2019

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Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis

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

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

Inflammatory Bowel Disease and Guillain Barre Syndrome in FCHO1 Deficiency

ILC3 deficiency and generalized ILC abnormalities in DOCK8‐deficient patients

Lymphoma Predisposing Gene in an Extended Family: CD70 Signaling Defect

Primary antibody deficiencies in Turkey: molecular and clinical aspects

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

Correction to: Primary antibody deficiencies in Turkey: molecular and clinical aspects

Successful rapid desensitization of a pediatric multiple sclerosis patient with anaphylaxis to ocrelizumab

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

Exaggerated T Follicular Helper Cell Responses in LRBA Deficiency Due to Failure of CTLA4-Mediated Regulation

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

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

Serving Healthy (?) Food on Toxic Plates

Lymphocyte Subset Abnormalities in Pediatric-Onset Common Variable Immunodeficiency

Chronic Rhinosinusitis in Patients with Primary Immunodeficiency

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

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

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

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

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

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

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

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

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