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List of works by Necil Kutukculer

A Clinical and Laboratory Approach to the Evaluation of Innate Immunity in Pediatric CVID Patients

scientific article published on 27 April 2015

Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency

scientific article published on 22 June 2019

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

scientific article published on 14 October 2018

An inherited immunoglobulin class-switch recombination deficiency associated with a defect in the INO80 chromatin remodeling complex

scientific article

Association of clinical and genetical features in FMF with focus on MEFV strip assay sensitivity in 452 children from western Anatolia, Turkey

scientific article published on 5 November 2011

Associations of interleukin (IL)-1β, IL-1 receptor antagonist, and IL-10 with dental caries

scientific article published on January 2015

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

scholarly article by Jacinta Bustamante et al published July 2007 in The Journal of Allergy and Clinical Immunology

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

scientific article published on 18 December 2015

Clinical and laboratory evaluation of periodically monitored Turkish children with IgG subclass deficiencies.

scientific article published on March 2009

Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiency

scientific article

Clinical picture and treatment of 2212 patients with common variable immunodeficiency

scientific article published on 28 February 2014

Comprehensive analysis of a large-scale screen for MEFV gene mutations: do they truly provide a "heterozygote advantage" in Turkey?

scientific article published on 17 March 2011

Consanguinity rate and delay in diagnosis in Turkish patients with combined immunodeficiencies: a single-center study

scientific article published on 6 October 2010

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

scientific article published on 04 May 2020

Cutaneous leukocytoclastic vasculitis in a child with interleukin-12 receptor beta-1 deficiency

scientific article published in March 2006

DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation

scientific article

Decreased ratio of CD4/CD8 lymphocytes might be predictive for successful interferon alpha and lamivudine combined therapy in childhood chronic hepatitis B infection: A preliminary study

scientific article published in June 2003

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

scientific article published on 24 May 2016

Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

scientific article

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

scientific article published on 04 August 2019

Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency

scientific article published in February 2003

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

scientific article

Does OM-85 BV prophylaxis trigger autoimmunity in IgA deficient children?

scientific article published on 21 July 2011

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

scientific article published on 17 September 2013

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

scientific article published on 6 September 2016

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

scientific article published on 01 January 2018

Fcγ receptor polymorphisms in patients with transient hypogammaglobulinemia of infancy presenting with mild and severe infections

scientific article published on December 2015

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

scientific article published on 13 November 2017

Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndrome.

scientific article

Granulomatous skin lesions, severe scrotal and lower limb edema due to mycobacterial infections in a child with complete IFN-γ receptor-1 deficiency.

scientific article

Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant

scientific article published on 25 August 2020

Hypercoagulability: interaction between inflammation and coagulation in familial Mediterranean fever

scientific article published on 24 May 2006

IL-12Rβ1 deficiency in two of fifty children with severe tuberculosis from Iran, Morocco, and Turkey

scientific article (publication date: 13 April 2011)

Immunodeficiency in a Child with Alström Syndrome

scientific article published on 28 August 2018

Increased PI3K/Akt activity and deregulated humoral immune response in human PTEN deficiency.

scientific article published on 13 August 2016

Increased percentages of autoantibodies in immunoglobulin A-deficient children do not correlate with clinical manifestations

scientific article published in January 2009

Increases in serum immunoglobulins to age-related normal levels in children with IgA and/or IgG subclass deficiency

scientific article published on March 2007

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

scientific article published on March 2015

Interleukin-1 receptor antagonist deficiency with a novel mutation; late onset and successful treatment with canakinumab: a case report

scientific article published on 23 June 2015

Inverse relationship between the ratio of ICAM-1 expressing lymphocytes and serum TGF-beta 1 concentrations in acute rheumatic fever

scientific article

Juvenile dermatomyositis with a rare and remarkable complication: sinus bradycardia

scientific article published on 30 August 2006

Juvenile psoriatic arthritis carrying familial Mediterranean fever gene mutations in a 14-year-old Turkish girl.

scientific article published on May 2007

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

scientific article

Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score

scientific article published on 27 December 2019

Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation

scientific article

Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications

scientific article

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

scientific article published on 10 January 2017

New laboratory findings in Turkish patients with transient hypogammaglobulinemia of infancy

scientific article published in December 2010

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

scientific article

Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation

scientific article published on 20 August 2013

Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication

scientific article published on 13 June 2017

Prospective, randomized comparison of OM-85 BV and a prophylactic antibiotic in children with recurrent infections and immunoglobulin A and/or G subclass deficiency

scientific article published on September 2003

Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis

scientific article published on 20 March 2016

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

scientific article published in April 2017

Relapsing polychondritis in a child with common variable immunodeficiency

scientific article published on 01 May 2009

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

scientific article

Study of patients with Hyper-IgM type IV phenotype who recovered spontaneously during late childhood and review of the literature

scientific article published on 28 January 2011

Successful management of colchicine resistant familial Mediterranean fever patients with a standardized canakinumab treatment protocol: a case series and literature review

scientific article published on 04 July 2019

TNFRSF13B/TACI Alterations in Turkish Patients with Common Variable Immunodeficiency and IgA Deficiency

scientific article published on 01 July 2018

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

scientific article published on 17 March 2020

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

scientific article

The outcome of patients with unclassified hypogammaglobulinemia in early childhood

scientific article published on 31 January 2009

The prevalences [correction] and patient characteristics of primary immunodeficiency diseases in Turkey--two centers study

scientific article

Two cases of macrocephaly and immune deficiency

scientific article published on April 2007

Two male siblings with a novel LRBA mutation presenting with different findings of IPEX syndrome

scientific article published on 15 October 2018

Value of biochemical markers for outcome in term infants with asphyxia.

scientific article published on November 2004

X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis

scientific article

X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production

scientific article

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