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Experimental Investigation of Microfluidic Device for Platelet Activation

IEEE transactions on biomedical engineering, 2023-03, Vol.70 (3), p.954-961

2023

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Role of natural killer cells in lung cancer

Journal of cancer research and clinical oncology, 2018-06, Vol.144 (6), p.997-1003

2018

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Biallelic Form of a Known CD3E Mutation in a Patient with Severe Combined Immunodeficiency

Journal of clinical immunology, 2020-04, Vol.40 (3), p.539-542

2020

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Invasive Saprochaete capitata Infection in a Patient with Autosomal Recessive CARD9 Deficiency and a Review of the Literature

Journal of clinical immunology, 2020-04, Vol.40 (3), p.466-474

2020

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Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R

Haematologica (Roma), 2015-06, Vol.100 (6), p.e216

2015

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COVID-19 Induced Hemophagocytic Lymphohistiocytosis in a Patient with Novel Homozygous UNC13D Gene Variant

Klinische Padiatrie, 2023-07, Vol.235 (4), p.258

2023

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A Novel Homozygous Six Base Pair Deletion Found in the NFATC2 Gene in a Patient with EBV-Associated Lymphoproliferation

Journal of clinical immunology, 2024-03, Vol.44 (3), p.74-74, Article 74

2024

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STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation

Clinical immunology (Orlando, Fla.), 2015-12, Vol.161 (2), p.316-323

2015

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Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre

Clinical and experimental immunology, 2024-02, Vol.215 (2), p.160-176

2024

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Necessity of Keratinized Tissues for Dental Implants: A Clinical, Immunological, and Radiographic Study

Clinical implant dentistry and related research, 2015-02, Vol.17 (1), p.1-12

2015

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A Novel Homozygous Germline Mutation in Transferrin Receptor 1 (TfR1) Leads to Combined Immunodeficiency and Provides New Insights into Iron-Immunity Axis

Journal of clinical immunology, 2024-02, Vol.44 (2), p.55-55, Article 55

2024

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Two siblings with PRKDC defect who presented with cutaneous granulomas and review of the literature

Clinical immunology (Orlando, Fla.), 2018-12, Vol.197, p.1-5

2018

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IgE and IgG4 binding to lentil epitopes in children with red and green lentil allergy

Pediatric allergy and immunology, 2020-02, Vol.31 (2), p.158-166

2020

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

Clinical immunology (Orlando, Fla.), 2023-10, Vol.255, p.109757-109757, Article 109757

2023

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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

Journal of clinical immunology, 2024-10, Vol.44 (7), p.157, Article 157

2024

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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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Corrigendum to “Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients” [Clinical Immunology 255 (2023) 109757]

Clinical immunology (Orlando, Fla.), 2023-11, Vol.256, p.109799-109799, Article 109799

2023

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Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD

Journal of clinical immunology, 2017-04, Vol.37 (3), p.269-272

2017

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Statins and IL-1β, IL-10, and MPO Levels in Gingival Crevicular Fluid: Preliminary Results

Inflammation, 2016-08, Vol.39 (4), p.1547-1557

2016

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Necessity of Keratinized Tissues for Dental Implants: A Clinical, Immunological, and Radiographic Study: Dental Implants and Keratinized Tissue Width

Clinical implant dentistry and related research, 2015-02, Vol.17 (1), p.1-12

2015

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C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma

Clinical rheumatology, 2012-07, Vol.31 (7), p.1123-1126

2012

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Statins and IL-1[beta], IL-10, and MPO Levels in Gingival Crevicular Fluid: Preliminary Results

Inflammation, 2016-08, Vol.39 (4), p.1547

2016

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Defective pneumococcal antibody response in patients with recurrent respiratory tract infections

Turkish journal of pediatrics, 2017, Vol.59 (5), p.555-560

2017

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Biallelic Form of a Known CD3E Mutation in a Patient with Severe Combined Immunodeficiency

Journal of clinical immunology, 2020, Vol.40 (3), p.539-542

2020

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Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD

Journal of clinical immunology, 2017, Vol.37 (3), p.269-272

2017

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Experimental Investigation of Microfluidic Device for Platelet Activation

Role of natural killer cells in lung cancer

Biallelic Form of a Known CD3E Mutation in a Patient with Severe Combined Immunodeficiency

Invasive Saprochaete capitata Infection in a Patient with Autosomal Recessive CARD9 Deficiency and a Review of the Literature

Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R

COVID-19 Induced Hemophagocytic Lymphohistiocytosis in a Patient with Novel Homozygous UNC13D Gene Variant

A Novel Homozygous Six Base Pair Deletion Found in the NFATC2 Gene in a Patient with EBV-Associated Lymphoproliferation

STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation

Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre

Necessity of Keratinized Tissues for Dental Implants: A Clinical, Immunological, and Radiographic Study

A Novel Homozygous Germline Mutation in Transferrin Receptor 1 (TfR1) Leads to Combined Immunodeficiency and Provides New Insights into Iron-Immunity Axis

Two siblings with PRKDC defect who presented with cutaneous granulomas and review of the literature

IgE and IgG4 binding to lentil epitopes in children with red and green lentil allergy

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

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

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

Corrigendum to “Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients” [Clinical Immunology 255 (2023) 109757]

Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD

Statins and IL-1β, IL-10, and MPO Levels in Gingival Crevicular Fluid: Preliminary Results

Necessity of Keratinized Tissues for Dental Implants: A Clinical, Immunological, and Radiographic Study: Dental Implants and Keratinized Tissue Width

C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma

Statins and IL-1[beta], IL-10, and MPO Levels in Gingival Crevicular Fluid: Preliminary Results

Defective pneumococcal antibody response in patients with recurrent respiratory tract infections

Biallelic Form of a Known CD3E Mutation in a Patient with Severe Combined Immunodeficiency

Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD

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