N. Kutukculer

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DOCK8 Functions as an Adaptor that Links TLR–MyD88 Signaling to B Cell Activation

Schneider, Douglas R. McDonald, Ghassan, 2012 .

DOCK 8 functions as an adaptor that links Toll-like receptor – MyD 88 signaling to B cell activation

Douglas R. McDonald, L. Notarangelo, A. Plebani, 2012 .

Low Penetrance, Broad Resistance, and Favorable Outcome of Interleukin 12 Receptor β1 Deficiency

Sami Al-Hajjar, A. Fischer, J. Casanova, 2003, The Journal of Experimental Medicine.

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

Sami Al-Hajjar, A. Fischer, J. Casanova, 2003, The Journal of experimental medicine.

Assessment of neutrophil chemotaxis and random migration in children with thalassemia major.

N. Kutukculer, O. Kutlu, N. Cetingul, 1996, Pediatric hematology and oncology.

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

N. Kutukculer, G. Aksu, Sanem Eren Akarcan, 2019, Rheumatology International.

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

N. Kutukculer, G. Aksu, N. Gulez, 2012, Clinical Rheumatology.

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

N. Kutukculer, B. Sozeri, A. Berdeli, 2011, Genetic testing and molecular biomarkers.

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

N. Kutukculer, L. Midyat, N. Karaca, 2007, The Journal of dermatology.

Hypercoagulability: interaction between inflammation and coagulation in familial Mediterranean fever

K. Kavaklı, N. Kutukculer, G. Aksu, 2007, Clinical Rheumatology.

In vitro T lymphocyte proliferation by carboxyfluorescein diacetate succinimidyl ester method is helpful in diagnosing and managing primary immunodeficiencies

N. Kutukculer, G. Aksu, E. Azarsız, 2018, Journal of clinical laboratory analysis.

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

N. Kutukculer, G. Aksu, N. Gulez, 2011, International immunopharmacology.

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

N. Kutukculer, G. Aksu, N. Gulez, 2009, Autoimmunity.

Juvenile dermatomyositis with a rare and remarkable complication: sinus bradycardia

N. Kutukculer, G. Aksu, N. Karaca, 2006, Rheumatology International.

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

A. Schäffer, V. Lougaris, R. Geha, 2015, The Journal of allergy and clinical immunology.

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

N. Kutukculer, G. Aksu, S. Tanriverdi, 2011, Case reports in medicine.

Three Different Classifications, B Lymphocyte Subpopulations, TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) Gene Mutations, CTLA-4 and ICOS Gene Polymorphisms in Turkish Patients with Common Variable Immunodeficiency

N. Kutukculer, G. Aksu, N. Gulez, 2012, Journal of Clinical Immunology.

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

M. van der Burg, B. Tóth, N. Kutukculer, 2011, Molecular immunology.

Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency.

İ. Reisli, T. Chatila, A. Al-Shaibi, 2019, The journal of allergy and clinical immunology. In practice.

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

J. Casanova, J. Bustamante, N. Kutukculer, 2012, Immunotherapy.

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

J. Casanova, C. Çavuşoğlu, B. Karapinar, 2006, The Journal of pediatrics.

Mycobacterium fortuitum-chelonae complex infection in a child with complete interleukin-12 receptor beta 1 deficiency.

J. Casanova, F. Altare, C. Çavuşoğlu, 2001, The Pediatric infectious disease journal.

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

N. Kutukculer, G. Aksu, A. Durmaz, 2022, Case reports in immunology.

The influence of marginal zinc deficient diet on post-vaccination immune response against hepatitis B in rats.

N. Kutukculer, G. Aksu, F. Kırkpınar, 2006, Hepatology research : the official journal of the Japan Society of Hepatology.

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

Faith Unal, N. Kutukculer, G. Aksu, 2003, Journal of gastroenterology and hepatology.

T-cell subsets and interleukin-6 response in Rasmussen's encephalitis.

O. Kitis, S. Gökben, N. Kutukculer, 2005, Pediatric neurology.

Major histocompatibility complex antigens and immune mechanisms in steroid‐responsive nephrotic syndrome

K. Kavaklı, N. Kutukculer, S. Mir, 1994, Acta paediatrica Japonica : Overseas edition.

Gingival crevicular fluid and serum hCAP18/LL-37 levels in generalized aggressive periodontitis

H. Atmaca, G. Emingil, N. Kutukculer, 2016, Clinical Oral Investigations.

Does smoking affect gingival crevicular fluid LL-37 levels following non-surgical periodontal treatment in chronic periodontitis?

G. Emingil, N. Kutukculer, E. Azarsız, 2016, Archives of oral biology.

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

N. Kutukculer, F. Ozkinay, D. Çoğulu, 2015, Journal of oral science.

Major histocompatibility complex antigens in Turkish children with steroid-responsive nephrotic syndrome

K. Kavaklı, N. Kutukculer, S. Mir, 1994, Pediatric Nephrology.

Clinical picture and treatment of 2212 patients with common variable immunodeficiency.

É. Oksenhendler, P. Soler-Palacín, A. Šedivá, 2014, The Journal of allergy and clinical immunology.

Adequate immune response to tetanus toxoid and failure of vitamin A and E supplementation to enhance antibody response in healthy children.

N. Kutukculer, Z. Kurugöl, S. Çaǧlayan, 2000, Vaccine.

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

N. Kutukculer, G. Aksu, N. Gulez, 2012, Italian Journal of Pediatrics.

The outcome of patients with unclassified hypogammaglobulinemia in early childhood

N. Kutukculer, N. Gulez, 2009, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

J. Casanova, J. Emile, A. Chapgier, 2007, The Journal of allergy and clinical immunology.

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

A. Gewies, D. Krappmann, N. Kutukculer, 2020, Journal of Allergy and Clinical Immunology.

Study of pro-inflammatory (TNF-α, IL-1α, IL-6) and T-cell-derived (IL-2, IL-4) cytokines in plasma and synovial fluid of patients with juvenile chronic arthritis: Correlations with clinical and laboratory parameters

N. Kutukculer, S. Çaǧlayan, F. Aydoğdu, 2005, Clinical Rheumatology.

Plasma and synovial fluid soluble CD23 concentrations in children with juvenile chronic arthritis.

N. Kutukculer, S. Çaǧlayan, 1998, Autoimmunity.

Do Elevated Serum IgM Levels Have to Be Included in Probable Diagnosis Criteria of Patients with Ataxia-Telangiectasia?

N. Kutukculer, G. Aksu, N. Gulez, 2014, International journal of immunopathology and pharmacology.

FONTANA et al. DCs DEFECT IN CD40-DEFICIENT PATIENTS Regular manuscript: IMMUNOBIOLOGY Functional defects of dendritic cells in CD40-deficient patients

A. Plebani, W. Vermi, F. Facchetti, 2003 .

Levels of ll-37 antimicrobial peptide in the gingival crevicular fluid of young and middle-aged subjects with or without gingivitis

H. Atmaca, N. Kutukculer, G. Atilla, 2016, Journal of Istanbul University Faculty of Dentistry.

Mid-Regional Proadrenomedullin Levels in Primary Immunodeficiencies Complicated with Pulmonary Manifestations

N. Kutukculer, E. Azarsız, N. Karaca, 2022, Indian Journal of Clinical Biochemistry.

DOCK8 Regulates STAT3 Activation and Promotes Th17 Cell Differentiation

R. Geha, İ. Reisli, W. Al-Herz, 2016 .

Defects Along the Th17 Differentiation Pathway Underlie Genetically Distinct Forms of the Hyper IgE Syndrome

İ. Reisli, T. Chatila, A. Somer, 2010 .

Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients

R. Schmidt, A. Plebani, J. Litzman, 2013, Clinical and experimental 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

N. Kutukculer, G. Aksu, E. Azarsız, 2016, International journal of immunopathology and pharmacology.

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

T. Hirschmugl, N. Kutukculer, K. Boztug, 2016, Case reports in immunology.

Comparing the levels of CTLA‐4‐dependent biological defects in patients with LRBA deficiency and CTLA‐4 insufficiency

İ. Reisli, A. Yildiran, S. Barış, 2022, Allergy.

Increased Gastric Production of Platelet-Activating Factor, Leukotriene-B4, and Tumor Necrosis Factor-α in Children with Helicobacter pylori Infection

N. Kutukculer, S. Aydoğdu, R. Yağcı, 1998, Digestive Diseases and Sciences.

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

J. Casanova, A. Puel, N. Kutukculer, 2017, Case reports in immunology.

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

L. Notarangelo, J. Chou, C. Cunningham-Rundles, 2017, The Journal of allergy and clinical immunology.

527 Low Penetrance, Broad Resistance, and Favorable Outcome of Interleukin 12 Receptor (cid:2) 1 Deﬁciency: Medical and Immunological

Sami Al-Hajjar, F. Deist, J. Casanova, 2003 .

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

N. Kutukculer, G. Aksu, H. El-Shanti, 2015, Journal of Medical Case Reports.

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

J. Franco, Y. Lau, O. Sanal, 2017, Front. Immunol..

Renal allograft rejection: the temporal relationship and predictive value of plasma TNF (alpha and beta), IFN-gamma and soluble ICAM-1

J. Kirby, J. Forsythe, B. Shenton, 1995 .

Renal Involvement as a Rare Complication of Dorfman–Chanarin Syndrome: A Case Report

N. Kutukculer, G. Aksu, Y. Bulut, 2008, Pediatric dermatology.

Progressive morphea of early childhood tracing Blaschko’s lines on the face: involvement of X chromosome monosomy in pathogenesis and clinical prognosis

N. Kutukculer, G. Aksu, F. Ozkinay, 2011, International journal of dermatology.

The effect of clotting factor concentrates on the immune system in HIV‐negative haemophilics

K. Kavaklı, C. Balkan, N. Kutukculer, 2005, Haemophilia : the official journal of the World Federation of Hemophilia.

Antı-β2 Glycoprotein I Antibodies in Children with Rheumatologic Disorders

N. Kutukculer, G. Aksu, E. Azarsız, 2017, Indian Journal of Clinical Biochemistry.

Autoantibodies Other than Antineutrophil Cytoplasmic Antibodies Are Not Positive in Patients with Psoriasis Vulgaris

N. Kutukculer, G. Aksu, S. Alper, 2005, The Journal of dermatology.

Inverse relationship between the ratio of ICAM-1 expressing lymphocytes and serum TGF-β1 concentrations in acute rheumatic fever

N. Kutukculer, G. Aksu, N. Bayram, 2005 .

Fc gamma RIIa, IIIa and IIIb polymorphisms in Turkish children susceptible to recurrent infectious diseases

N. Kutukculer, G. Aksu, A. Berdeli, 2006, Clinical and Experimental Medicine.

Consanguinity Rate and Delay in Diagnosis in Turkish Patients with Combined Immunodeficiencies: a Single-Center Study

N. Kutukculer, G. Aksu, N. Gulez, 2011, Journal of Clinical Immunology.

Salivary and gastric fluid secretory immunoglobulin A and free secretory component concentrations in children with Helicobacter pylori-positive gastritis.

N. Kutukculer, S. Aydoğdu, R. Yağcı, 1998, Journal of tropical pediatrics.

Periodic fever syndromes: a patient diagnosed with recurrent Kawasaki disease

N. Kutukculer, E. Levent, Eser Doğan, 2020, Cardiology in the Young.

A Case with Omenn Syndrome

N. Kutukculer, F. Ozkinay, M. Yalaz, 2013 .

Revisiting Human IL-12R&bgr;1 Deficiency: A Survey of 141 Patients From 30 Countries

Smita Y. Patel, A. Al-ghonaium, Sami Al-Hajjar, 2010, Medicine.

Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages

N. Kutukculer, G. Aksu, E. Azarsız, 2019, Scandinavian journal of immunology.

A novel Y331X nonsense mutation in TNFRSF1A gene in two unrelated Turkish families with periodic fever syndrome

N. Kutukculer, G. Aksu, N. Gulez, 2010, International journal of immunogenetics.

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

C. Eraslan, N. Kutukculer, G. Aksu, 2017, Case reports in immunology.

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

N. Kutukculer, G. Aksu, N. Gulez, 2021, Asian Pacific journal of allergy and immunology.

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

J. Casanova, J. Franco, B. Boisson, 2013, Blood.

Initial presenting manifestations in 16,486 patients with Inborn Errors of Immunity include infections and non-infectious manifestations.

Nurit Assia Batzir, K. Schwarz, D. Foell, 2021, The Journal of allergy and clinical immunology.

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

J. Casanova, J. Franco, C. Picard, 2014, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

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

L. Notarangelo, A. Plebani, N. Kutukculer, 2003, The Journal of pediatrics.

The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study

S. Barış, N. Kutukculer, C. Aytekin, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

Edward R B McCabe, Bodo Grimbacher, Christoph Klein, 2009, The Journal of allergy and clinical immunology.

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

T. Chatila, M. Yılmaz, A. Somer, 2009, The Journal of allergy and clinical immunology.

Immunoglobulin Light Chain Levels Can Be Used to Determine Disease Stage in Children with Juvenile Idiopathic Arthritis

N. Kutukculer, G. Aksu, N. Gulez, 2011, American Society for Clinical Laboratory Science.

Evaluation of the relationship between caries indices and salivary secretory IgA, salivary pH, buffering capacity and flow rate in children with Down's syndrome.

N. Kutukculer, F. Ozkinay, D. Çoğulu, 2006, Archives of oral biology.

Comparative evaluation of pro-inflammatory cytokine levels in pulpotomized primary molars.

N. Kutukculer, T. Kose, C. Eronat, 2015, Journal of oral science.

Video display terminal — the risk of trisomy 18?

N. Kutukculer, N. Kultursay, F. Koprubasi, 1994, Clinical genetics.

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

T. Chatila, S. Holland, C. Klein, 2009, The Journal of allergy and clinical immunology.

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

Hao Wu, R. Geha, W. Al-Herz, 2016, The Journal of allergy and clinical immunology.

IL-12Rβ1 Deficiency in Two of Fifty Children with Severe Tuberculosis from Iran, Morocco, and Turkey

J. Casanova, A. Bousfiha, L. Abel, 2011, PloS one.

Arg753Gln Polymorphism of the Human Toll-like Receptor-2 Gene in Children with Recurrent Febrile Infections

N. Kutukculer, G. Aksu, A. Berdeli, 2007, Biochemical Genetics.

Cerebrospinal fluid interleukin-6 levels in patients with west syndrome

N. Kutukculer, H. Tekgul, G. Serdaroğlu, 2006, Brain and Development.

Griscelli syndrome: Report of a case and review of the literature

Remziye Deveci, S. Karaçalı, F. Vardar, 2001, Pediatrics international : official journal of the Japan Pediatric Society.

Plasma interleukin-3 and interleukin-4 concentrations in Turkish asthmatic children.

N. Kutukculer, R. Tanaç, E. Demir, 1995, Archives of disease in childhood.

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

J. Casanova, A. Bousfiha, F. Ailal, 2015, Immunological reviews.

Quinacrine‐induced psychiatric disturbances in a child with common variable immunodeficiency and chronic giardiasis

N. Kutukculer, G. Aksu, S. Erermiş, 2002, Human psychopharmacology.

THE VALUE OF POSTTRANSPLANT MONITORING OF INTERLEUKIN (IL)-2, IL‐3, IL‐4, IL‐6, IL‐8, AND SOLUBLE CD23 IN THE PLASMA OF RENAL ALLOGRAFT RECIPIENTS

J. Forsythe, K. Rigg, N. Kutukculer, 1995, Transplantation.

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

C. Bodemer, J. Casanova, A. Israël, 2006, The Journal of experimental medicine.

Consensus Middle East and North Africa Registry on Inborn Errors of Immunity

R. Geha, A. Bousfiha, W. Al-Herz, 2021, Journal of Clinical Immunology.

A Novel Homozygous TRNT1 Mutation in a Child With an Early Diagnosis of Common Variable Immunodeficiency Leading to Mild Hypogammaglobulinemia and Hemolytic Anemia.

N. Kutukculer, G. Aksu, A. Durmaz, 2021, Journal of pediatric hematology/oncology.

Serum immunoglobulins, IgG subclasses, isohemagglutinins and complement-3 levels in patients with thalassemia major

C. Vergin, N. Kutukculer, N. Cetingul, 1997, Indian journal of pediatrics.

Specific antibody response in children with thalassemia major.

C. Vergin, N. Çetingül, K. Kavaklı, 1997, Pediatric hematology and oncology.

Constrictive Aspergillosis Pericarditis

N. Kutukculer, G. Aksu, N. Karaca, 2019, Pediatric Immunology.

Hyper‐Immunoglobulin M Syndrome Type 3 with Normal CD40 Cell Surface Expression

M. Forveille, A. Durandy, N. Kutukculer, 2012, Scandinavian journal of immunology.

Dock8 Functions as an Adaptor That Links Toll-like Receptor– Myd88 Signaling to B Cell Activation Hhs Public Access

Alessandro Plebani, Rima Wakim, Kate Fitzgerald, 2022 .

First report of successful stem cell transplantation in a child with CD40 deficiency

S. Giliani, G. Lanzi, N. Kutukculer, 2007, Bone Marrow Transplantation.

Outcome of hematopoietic stem cell transplantation in hyper-IgM syndrome caused by CD40 deficiency.

L. Notarangelo, N. Kutukculer, N. Cetingul, 2003, The Journal of pediatrics.

Necrotizing Liver Granuloma

N. Kutukculer, G. Aksu, N. Karaca, 2019, Pediatric Immunology.

Immune deficiencies , infection , and systemic immune disorders Defects along the TH 17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

T. Chatila, M. Yılmaz, A. Somer, 2009 .

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

N. Kutukculer, G. Aksu, A. Berdeli, 2016, Journal of clinical medicine research.

Simple Measurement of IgA Predicts Immunity and Mortality in Ataxia-Telangiectasia

A. Plebani, C. Pignata, S. Reda, 2021, Journal of Clinical Immunology.

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

N. Kutukculer, G. Aksu, N. Gulez, 2009, Clinical and Experimental Medicine.

Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry.

R. Geha, J. Chou, W. Al-Herz, 2022, Clinical immunology.

N. Kutukculer, G. Aksu, N. Gulez, 2012, Journal of Clinical Immunology.

X-linked agammaglobulinemia: ınvestigation of clinical and laboratory findings, novel gene mutations and prevention of ınfective complications in long-term follow-up.

N. Kutukculer, G. Aksu, A. Durmaz, 2021, American journal of clinical and experimental immunology.

Relapsing polychondritis in a child with common variable immunodeficiency

N. Kutukculer, G. Aksu, N. Gulez, 2009, International journal of dermatology.

The Prevalances and Patient Characteristics of Primary Immunodeficiency Diseases in Turkey—Two Centers Study

N. Kutukculer, G. Aksu, S. Kilic, 2012, Journal of Clinical Immunology.

Lymphocyte subsets in Bell's palsy: immune pathogenesis and outcome prediction.

S. Gökben, N. Kutukculer, M. Yalaz, 2004, Pediatric neurology.

Celiac disease in children with Down syndrome: Importance of follow‐up and serologic screening

N. Kutukculer, S. Aydoğdu, F. Ozkinay, 2003, Pediatrics international : official journal of the Japan Pediatric Society.

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

N. Kutukculer, M. Yalaz, N. Kultursay, 2004, Pediatric neurology.

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

A. Fischer, Z. Herceg, M. Nussenzweig, 2015, The Journal of allergy and clinical immunology.

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

A. Gennery, A. Worth, L. Hammarström, 2019, The Journal of allergy and clinical immunology.

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

E. Gambineri, N. Kutukculer, G. Aksu, 2018, JMM case reports.

Lymphocyte Subsets and Plasma IL-1 α, IL-2, and TNF-α Concentrations in Acute Rheumatic Fever and Chronic Rheumatic Heart Disease

N. Narin, N. Kutukculer, A. Bakiler, 1995 .

Functional defects of dendritic cells in patients with CD40 deficiency.

L. Notarangelo, A. Plebani, R. Badolato, 2003, Blood.

Functional defects of dendritic cells in CD 40-deficient patients

A. Plebani, W. Vermi, F. Facchetti, 2003 .

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

N. Kutukculer, G. Aksu, A. Berdeli, 2020, Clinical case reports.

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

N. Kutukculer, G. Aksu, E. Azarsız, 2018, Avicenna journal of medical biotechnology.

Maternally acquired varicella-zoster virus antibodies disappear at 6 months of age in prematurely born children.

N. Kutukculer, G. Aksu, M. Yalaz, 2003, Panminerva medica.

Early-Onset Inflammatory Bowel Disease

N. Kutukculer, G. Aksu, N. Karaca, 2019, Pediatric Immunology.

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

M. van der Burg, M. Wentink, J. V. van Dongen, 2016, The Journal of allergy and clinical immunology.

A Novel TTC37 Mutation Causing Remarkable Trichohepatoenteric Syndrome Clinical Findings Such as Pyoderma Gangrenosum and Immunodeficiency without Severe Diarrhea.

N. Kutukculer, G. Aksu, N. Karaca, 2019, Journal of investigational allergology & clinical immunology.

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

N. Kutukculer, F. Genel, 2003, Current therapeutic research, clinical and experimental.

Evaluation of Serum Anti‐Cardiolipin and Oxidized Low‐Density Lipoprotein Levels in Chronic Periodontitis Patients With Essential Hypertension

N. Kutukculer, N. Barış, G. Atilla, 2008 .

Economic Burden of Primary Immunodeficiency (PIDD) In Turkey

I. Tezcan, N. Kutukculer, A. Ikinciogullari, 2016 .

The Prevalances and Patient Characteristics of Primary Immunodeficiency Diseases in Turkey—Two Centers Study

N. Kutukculer, G. Aksu, S. Kilic, 2012, Journal of Clinical Immunology.

Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe

P. Kralickova, J. Litzman, A. Turley, 2015, Journal of Clinical Immunology.

The correlation between serum immunoglobulin A and immunoglobulin G levels and the presence of Treponema denticola in human periapical lesions.

A. Uzel, N. Kutukculer, D. Çoğulu, 2007, Journal of endodontics.

Chitotriosidase enzyme activity: is this a possible chronic inflammation marker in children with common variable immunodeficiency and early atherosclerosis?

N. Kutukculer, E. Levent, E. Azarsız, 2017, Annals of clinical biochemistry.

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

N. Kutukculer, G. Aksu, E. Azarsız, 2015, Front. Immunol..

Does Intravenous Immunoglobulin Therapy Prolong Immunodeficiency in Transient Hypogammaglobulinemia of Infancy?

N. Kutukculer, G. Aksu, E. Azarsız, 2013, Pediatric reports.

New laboratory findings in Turkish patients with transient hypogammaglobulinemia of infancy.

N. Kutukculer, G. Aksu, N. Gulez, 2010, Iranian journal of allergy, asthma, and immunology.

Is There an Association between Autoimmune Hemolytic Anemia and Ataxia-Telangiectasia?

N. Kutukculer, G. Aksu, 2000, Autoimmunity.

22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management.

N. Kutukculer, G. Aksu, N. Gulez, 2021, Allergologia et Immunopathologia.

Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe

P. Kralickova, J. Litzman, N. Kutukculer, 2015, Journal of Clinical Immunology.

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

N. Kutukculer, G. Aksu, Ç. Aydoğmuş, 2022, Scandinavian journal of immunology.

Immune status and autoantibody formation in children with chronic hepatitis B infection.

Faith Unal, N. Kutukculer, G. Aksu, 2002, Panminerva medica.

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

N. Kutukculer, G. Aksu, N. Gulez, 2018, International journal of immunopathology and pharmacology.

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

N. Kutukculer, G. Aksu, A. Berdeli, 2015, Asian Pacific journal of allergy and immunology.

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

J. Casanova, A. Puel, N. Kutukculer, 2019, Case reports in immunology.

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

J. Casanova, A. Puel, T. Fukao, 2020, Journal of Clinical Immunology.

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

N. Kutukculer, G. Aksu, N. Karaca, 2007, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Pesticide-Induced Scleroderma and Early Intensive Immunosuppressive Treatment

T. Akalın, N. Kutukculer, G. Aksu, 2012, Archives of environmental & occupational health.

Immunodeficiency in a Child with Alström Syndrome

N. Kutukculer, G. Aksu, F. Ozkinay, 2018, The Indian Journal of Pediatrics.

Determination of cut‐off titers and agreement between immunofluorescence and immunoblotting methods for detecting antinuclear antibodies in children

N. Kutukculer, N. Gulez, G. Aksu, 2010, Journal of clinical laboratory analysis.

Antı-β2 Glycoprotein I Antibodies in Children with Rheumatologic Disorders

N. Kutukculer, G. Aksu, E. Azarsız, 2017, Indian Journal of Clinical Biochemistry.

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

A. Durandy, N. Kutukculer, G. Aksu, 2011, European Journal of Pediatrics.

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

N. Kutukculer, G. Aksu, N. Karaca, 2018, Case reports in immunology.

Different molecular behavior of CD40 mutants causing hyper-IgM syndrome.

M. Vihinen, L. Notarangelo, A. Plebani, 2010, Blood.

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

N. Kutukculer, G. Aksu, C. Karadeniz, 2009, Asian Pacific journal of allergy and immunology.

Gingival crevicular fluid and serum hCAP18/LL-37 levels in generalized aggressive periodontitis

H. Atmaca, G. Emingil, N. Kutukculer, 2017, Clinical Oral Investigations.

IgG-anti-IgA antibodies: an autoimmune finding in patients with psoriasis vulgaris.

N. Kutukculer, G. Aksu, İ. Ertam, 2012, Minerva medica.

Lymphocyte Subsets and Inflammatory Mediators in Patients With Subacute Sclerosing Panencephalitis

N. Kutukculer, G. Dizdarer, H. Tekgül, 1999, Journal of child neurology.

Granulomatous pyoderma preceding chronic recurrent multifocal osteomyelitis triggered by vaccinations in a two-year-old boy: a case report

N. Kutukculer, G. Aksu, N. Gulez, 2010, Journal of Medical Case Reports.

The effect of adjunctive chlorhexidine mouthrinse on clinical parameters and gingival crevicular fluid cytokine levels in untreated plaque-associated gingivitis

G. Emingil, N. Kutukculer, G. Atilla, 2009, Inflammation Research.

Association between anti-endomysial antibody and total intestinal villous atrophy in children with coeliac disease.

N. Kutukculer, G. Aksu, S. Aydoğdu, 2003, Journal of postgraduate medicine.

Idiopathic CD4+ T cell lymphocytopenia with the absence of B cells and CD8+28+ cells in peripheral blood

N. Kutukculer, G. Aksu, C. Ozturk, 2002, Clinical and Experimental Medicine.

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

N. Kutukculer, G. Aksu, A. Durmaz, 2023, Case reports in immunology.

Evaluation of Transforming Growth Factor-β1 Level in Crevicular Fluid of Cyclosporin A-Treated Patients

N. Buduneli, N. Kutukculer, G. Aksu, 2001 .

CLINICAL FEATURES OF CANDIDIASIS IN PATIENTS WITH INTERLEUKIN-12 RECEPTOR B1 DEFICIENCY

J. Casanova, C. Picard, L. Abel, 2012 .

Revisiting Human IL-12R&bgr;1 Deficiency: A Survey of 141 Patients From 30 Countries

Smita Y. Patel, A. Al-ghonaium, Sami Al-Hajjar, 2010, Medicine.

DOCK8 functions as an adaptor that links Toll-like receptor–MyD88 signaling to B cell activation

Douglas R. McDonald, L. Notarangelo, A. Plebani, 2012, Nature Immunology.

Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experience.

N. Kutukculer, G. Aksu, N. Karaca, 2023, Immunologic research.

Comparative evaluation of pro-inflammatory cytokine levels in pulpotomized primary molars.

N. Kutukculer, T. Kose, C. Eronat, 2015, Journal of oral science.

Renal allograft rejection: the temporal relationship and predictive value of plasma TNF (alpha and beta), IFN-gamma and soluble ICAM-1

N. Kutukculer, B. Shenton, G. Proud, 1995, Transplant international : official journal of the European Society for Organ Transplantation.

Primary immunodeficiency disorder.

N. Kutukculer, G. Aksu, E. Yilmaz, 2020, European annals of allergy and clinical immunology.

Chitotriosidase enzyme activity: is this a possible chronic inflammation marker in children with common variable immunodeficiency and early atherosclerosis?

N. Kutukculer, E. Levent, E. Azarsız, 2017, Annals of clinical biochemistry.

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

N. Kutukculer, G. Aksu, N. Gulez, 2009, Autoimmunity.

Granulomatous pyoderma preceding chronic recurrent multifocal osteomyelitis triggered by vaccinations in a two-year-old boy: a case report

N. Kutukculer, G. Aksu, N. Gulez, 2010, Journal of medical case reports.

Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients

R. Schmidt, A. Plebani, J. Litzman, 2013, Clinical and experimental immunology.

Facilitated Subcutaneous Immunoglobulin Treatment Increases the Quality of Life and Decreases the Number of Infections and Hospitalizations in Children with Primary Immunodeficiencies

N. Kutukculer, G. Aksu, E. Topyıldız, 2024, International Archives of Allergy and Immunology.

Dual Diagnosis of Trichohepatoenteric Syndrome and Lipoid Proteinosis in a Turkish Child

N. Kutukculer, G. Aksu, F. Ozkinay, 2023, Molecular Syndromology.