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CD4+CD25+Foxp3+ T regulatory cells, Th1 (CCR5, IL-2, IFN-γ) and Th2 (CCR4, IL-4, Il-13) type chemokine receptors and intracellular cytokines in children with common variable immunodeficiency

International journal of immunopathology and pharmacology, 2016-06, Vol.29 (2), p.241-251

2016

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The IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation

Journal of clinical immunology, 2020-05, Vol.40 (4), p.643-645

2020

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A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry

Orphanet journal of rare diseases, 2017-10, Vol.12 (1), p.167-167, Article 167

2017

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Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans

Proceedings of the National Academy of Sciences - PNAS, 2011-07, Vol.108 (28), p.11554-11559

2011

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ILC3 deficiency and generalized ILC abnormalities in DOCK8‐deficient patients

Allergy (Copenhagen), 2020-04, Vol.75 (4), p.921-932

2020

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Reference values for B-cell surface markers and co-receptors associated with primary immune deficiencies in healthy Turkish children

International journal of immunopathology and pharmacology, 2017-06, Vol.30 (2), p.194-200

2017

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An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission

Case Reports in Immunology, 2023-04, Vol.2023, p.2363760-6

2023

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Correction to: the IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic because of a Reinitiation of Translation

Journal of clinical immunology, 2020-05, Vol.40 (4), p.646-646

2020

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Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA‐2; PLCG2): Striking clinical phenotypic overlap and difference

Clinical case reports, 2021-04, Vol.9 (4), p.2023-2031

2021

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Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients

International journal of immunopathology and pharmacology, 2018-01, Vol.32, p.2058738418779458-2058738418779458

2018

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Early Immunomodulatory Effects of Different Natural Surfactant Preparations in Preterms With Respiratory Distress

Frontiers in pediatrics, 2022-03, Vol.10, p.845780-845780

2022

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A Novel BLNK Gene Mutation in a Four-Year-Old Child Who Presented with Late Onset of Severe Infections and High IgM Levels and Diagnosed and Followed as X-Linked Agammaglobulinemia for Two Years

Case Reports in Immunology, 2022-06, Vol.2022, p.1-6

2022

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BCG-osis and tuberculosis in a child with chronic granulomatous disease

Journal of allergy and clinical immunology, 2007-07, Vol.120 (1), p.32-38

2007

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Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases

Journal of allergy and clinical immunology, 2016-07, Vol.138 (1), p.241-248.e3

2016

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Deficiency of Interleukin-1 Receptor Antagonist: A Case with Late Onset Severe Inflammatory Arthritis, Nail Psoriasis with Onychomycosis and Well Responsive to Adalimumab Therapy

Case Reports in Immunology, 2019, Vol.2019 (2019), p.1-6

2019

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Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies

Case Reports in Immunology, 2017-01, Vol.2017 (2017), p.1-6

2017

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An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation

Case Reports in Immunology, 2018-01, Vol.2018 (2018), p.1-4

2018

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Evaluation of the immunomodulatory properties in mice and in vitro anti-inflammatory activity of cycloartane type saponins from Astragalus species

Journal of ethnopharmacology, 2012-01, Vol.139 (2), p.574-581

2012

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Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases

Case Reports in Immunology, 2016-01, Vol.2016 (2016), p.1-5

2016

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Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency

Italian journal of pediatrics, 2012-03, Vol.38 (1), p.8-8, Article 8

2012

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Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis

Molecular biology reports, 2024-12, Vol.51 (1), p.15-15, Article 15

2024

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Does intravenous immunoglobulin therapy prolong immunodeficiency in transient hypogammaglobulinemia of infancy?

Pediatric reports, 2013-09, Vol.5 (3), p.e14-e14

2013

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Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients

The journal of pediatric research, 2024-06, Vol.11 (2), p.110-117

2024

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Necrotizing Liver Granuloma/Abscess and Constrictive Aspergillosis Pericarditis with Central Nervous System Involvement: Different Remarkable Phenotypes in Different Chronic Granulomatous Disease Genotypes

Case Reports in Immunology, 2017-01, Vol.2017 (2017), p.1-9

2017

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New laboratory findings in Turkish patients with transient hypogammaglobulinemia of infancy

Iranian journal of allergy, asthma, and immunology, 2010-12, Vol.9 (4), p.237-243

2010

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CD4+CD25+Foxp3+ T regulatory cells, Th1 (CCR5, IL-2, IFN-γ) and Th2 (CCR4, IL-4, Il-13) type chemokine receptors and intracellular cytokines in children with common variable immunodeficiency

The IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation

A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry

Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans

ILC3 deficiency and generalized ILC abnormalities in DOCK8‐deficient patients

Reference values for B-cell surface markers and co-receptors associated with primary immune deficiencies in healthy Turkish children

An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission

Correction to: the IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic because of a Reinitiation of Translation

Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA‐2; PLCG2): Striking clinical phenotypic overlap and difference

Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients

Early Immunomodulatory Effects of Different Natural Surfactant Preparations in Preterms With Respiratory Distress

A Novel BLNK Gene Mutation in a Four-Year-Old Child Who Presented with Late Onset of Severe Infections and High IgM Levels and Diagnosed and Followed as X-Linked Agammaglobulinemia for Two Years

BCG-osis and tuberculosis in a child with chronic granulomatous disease

Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases

Deficiency of Interleukin-1 Receptor Antagonist: A Case with Late Onset Severe Inflammatory Arthritis, Nail Psoriasis with Onychomycosis and Well Responsive to Adalimumab Therapy

Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies

An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation

Evaluation of the immunomodulatory properties in mice and in vitro anti-inflammatory activity of cycloartane type saponins from Astragalus species

Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases

Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency

Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis

Does intravenous immunoglobulin therapy prolong immunodeficiency in transient hypogammaglobulinemia of infancy?

Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients

Necrotizing Liver Granuloma/Abscess and Constrictive Aspergillosis Pericarditis with Central Nervous System Involvement: Different Remarkable Phenotypes in Different Chronic Granulomatous Disease Genotypes

New laboratory findings in Turkish patients with transient hypogammaglobulinemia of infancy

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