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Dedicator of cytokinesis 8 regulates signal transducer and activator of transcription 3 activation and promotes TH17 cell differentiation

Journal of allergy and clinical immunology, 2016-11, Vol.138 (5), p.1384-1394.e2

2016

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The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

Journal of allergy and clinical immunology, 2015-08, Vol.136 (2), p.402-412

2015

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Mutations affecting the actin regulator WD repeat–containing protein 1 lead to aberrant lymphoid immunity

Journal of allergy and clinical immunology, 2018-11, Vol.142 (5), p.1589-1604.e11

2018

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

Journal of allergy and clinical immunology, 2009-12, Vol.124 (6), p.1289-1302.e4

2009

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Clinical, Molecular, Immunological Properties and Our Clinical Experiences in Patients Diagnosed with X-linked Agamaglobulinemia

Izmir Dr. Behçet Uz Çocuk Hastanesi dergisi, 2023-12, Vol.13 (3), p.185-191

2023

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Defects along the TH17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

Journal of allergy and clinical immunology, 2009-08, Vol.124 (2), p.342-348

2009

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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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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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Prevalence of Viruses in Acute Asthma Exacerbations in Childhood in a Hospital in West Part of Turkey

Iranian journal of allergy, asthma, and immunology, 2022-04, Vol.21 (2), p.112

2022

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Characteristics of the patients followed with the diagnosis of common variable immunodeficiency and the complications

Central-European journal of immunology, 2019-01, Vol.44 (2), p.119-126

2019

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The Significance of B-cell Subsets in Patients with Unclassified Hypogammaglobulinemia and Association with Intravenous Immunoglobulin Replacement Requirement

Iranian journal of immunology, 2018-03, Vol.15 (1), p.1-13

2018

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Letter to the Editor: Coexistence of Autoimmune Lymphoproliferative Syndrome and Familial Mediterranean Fever

Iranian journal of immunology, 2020-06, Vol.17 (2), p.172-174

2020

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Do microdeletions lead to immune deficiency?

Central-European journal of immunology, 2020-01, Vol.45 (1), p.69-72

2020

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Inherited Classical and Alternative Pathway Complement Deficiencies in Children: A Single Center Experience

Iranian journal of immunology, 2018-12, Vol.15 (4), p.309-320

2018

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Late diagnosis of leukocyte adhesion deficiency type II and Bombay blood type in a child: a rare case report

Central-European journal of immunology, 2019-01, Vol.44 (2), p.206-209

2019

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Parameters indicative of persistence of valvular pathology at initial diagnosis in acute rheumatic carditis: the role of albumin and CD19 expression

Jornal de pediatria, 2016-11, Vol.92 (6), p.581-587

2016

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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, p.5459029-5

2016

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Sydenham's chorea: clinical findings and comparison of the efficacies of sodium valproate and carbamazepine regimens

Brain & development (Tokyo. 1979), 2002-03, Vol.24 (2), p.73-76

2002

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Parameters indicative of persistence of valvular pathology at initial diagnosis in acute rheumatic carditis: the role of albumin and CD19 expression

Jornal de Pediatria (Versão em Português), 2016-11, Vol.92 (6), p.581-587

2016

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Interleukin‐12/‐23 receptor beta 1 deficiency in an infant with draining BCG lymphadenitis

Pediatrics international, 2009-04, Vol.51 (2), p.310-312

2009

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Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature

Asian Pacific journal of allergy and immunology, 2023-12, Vol.41 (4), p.372-378

2023

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Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID

Clinical and experimental medicine, 2009-12, Vol.9 (4), p.339-342, Article 339

2009

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DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients

Journal of clinical immunology, 2015-02, Vol.35 (2), p.189-198

2015

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Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variants

Immunologic research, 2024-04

2024

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Dedicator of cytokinesis 8 regulates signal transducer and activator of transcription 3 activation and promotes TH17 cell differentiation

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

Mutations affecting the actin regulator WD repeat–containing protein 1 lead to aberrant lymphoid immunity

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

Clinical, Molecular, Immunological Properties and Our Clinical Experiences in Patients Diagnosed with X-linked Agamaglobulinemia

Defects along the TH17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

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

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

Prevalence of Viruses in Acute Asthma Exacerbations in Childhood in a Hospital in West Part of Turkey

Characteristics of the patients followed with the diagnosis of common variable immunodeficiency and the complications

The Significance of B-cell Subsets in Patients with Unclassified Hypogammaglobulinemia and Association with Intravenous Immunoglobulin Replacement Requirement

Letter to the Editor: Coexistence of Autoimmune Lymphoproliferative Syndrome and Familial Mediterranean Fever

Do microdeletions lead to immune deficiency?

Inherited Classical and Alternative Pathway Complement Deficiencies in Children: A Single Center Experience

Late diagnosis of leukocyte adhesion deficiency type II and Bombay blood type in a child: a rare case report

Parameters indicative of persistence of valvular pathology at initial diagnosis in acute rheumatic carditis: the role of albumin and CD19 expression

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

Sydenham's chorea: clinical findings and comparison of the efficacies of sodium valproate and carbamazepine regimens

Parameters indicative of persistence of valvular pathology at initial diagnosis in acute rheumatic carditis: the role of albumin and CD19 expression

Interleukin‐12/‐23 receptor beta 1 deficiency in an infant with draining BCG lymphadenitis

Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature

Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID

CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients

Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variants

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