Lista de obras - Neslihan Edeer Karaca - Dominio Público Uruguay

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

artículo científico publicado en 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

artículo científico publicado en 2018

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

artículo científico publicado en 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

artículo científico publicado en 2015

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

artículo científico publicado en 2019

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

artículo científico publicado en 2009

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

artículo científico publicado en 2013

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

artículo científico publicado en 2010

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

artículo científico publicado en 2015

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

artículo científico publicado en 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

artículo científico publicado en 2010

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

artículo científico publicado en 2009

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

artículo científico publicado en 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

artículo científico publicado en 2016

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

artículo científico publicado en 2018

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

artículo científico publicado en 2015

Frequency of Mycobacterium bovis and mycobacteria in primary immunodeficiencies

artículo científico publicado en 2017

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

artículo científico publicado en 2017

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

artículo científico publicado en 2012

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

artículo científico publicado en 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.

artículo científico publicado en 2008

Immunodeficiency in a Child with Alström Syndrome

artículo científico publicado en 2018

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

artículo científico publicado en 2009

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

artículo científico publicado en 2007

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

artículo científico publicado en 2015

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

artículo científico publicado en 2015

Juvenile dermatomyositis with a rare and remarkable complication: sinus bradycardia

artículo científico publicado en 2006

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

artículo científico publicado en 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.

artículo científico publicado en 2016

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

artículo científico publicado en 2010

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

artículo científico publicado en 2012

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

artículo científico publicado en 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

artículo científico publicado en 2017

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

artículo científico publicado en 2022

Relapsing polychondritis in a child with common variable immunodeficiency

artículo científico publicado en 2009

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

artículo científico publicado en 2015

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

artículo científico publicado en 2011

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

artículo científico publicado en 2019

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

artículo científico publicado en 2018

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

artículo científico publicado en 2020

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

artículo científico publicado en 2012

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

artículo científico publicado en 2011

Lista de obras de Neslihan Edeer Karaca

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

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

Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Frequency of Mycobacterium bovis and mycobacteria in primary immunodeficiencies

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

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

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

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

Immunodeficiency in a Child with Alström Syndrome

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

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

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

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

Juvenile dermatomyositis with a rare and remarkable complication: sinus bradycardia

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

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

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

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

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

Psychological burden of pediatric primary immunodeficiency

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

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

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

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

Relapsing polychondritis in a child with common variable immunodeficiency

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

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

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

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

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

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

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

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