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List of works by Neslihan Edeer Karaca

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

scientific article published on 27 April 2015

A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature

scientific article published on 01 September 2020

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

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

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

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

scientific article published on 23 January 2019

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

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

scientific article published on 6 October 2010

DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients

scientific article

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

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

Determination of intracellular Th1/Th2 type cytokines in lymphocytes of chronic hepatitis B patients treated with interferon-alpha

scientific article published on 01 December 2010

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

Frequency of Mycobacterium bovis and mycobacteria in primary immunodeficiencies

scientific article published in September 2017

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

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

Human soluble tumor necrosis factor receptor I (sTNF-RI) and interleukin-I receptor antagonist (IL-I Ra) in different stages of acute rheumatic fever.

scientific article

Immunodeficiency in a Child with Alström Syndrome

scientific article published on 28 August 2018

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

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

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

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

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

Psychological burden of pediatric primary immunodeficiency

scientific article published on 04 October 2018

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

scientific article published on 20 March 2016

Recurrent infections, neurologic signs, low serum uric acid levels, and lymphopenia in childhood: Purine nucleoside phosphorylase deficiency, an emergency for infants

scientific article published on 23 September 2020

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

Regulatory B cells in patients suffering from inborn errors of immunity with severe immune dysregulation

scientific article published in 2022

Relapsing polychondritis in a child with common variable immunodeficiency

scientific article published on 01 May 2009

Rifampicin-resistant Mycobacterium bovis BCG strain isolated from an infant with NEMO mutation

scientific article published on April 2015

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 evaluation of malignancies in Turkish primary immunotherapy patients; a multicenter study

scientific article published on 14 February 2020

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

scientific article

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

scientific article published on 15 October 2018

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

scientific article

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