Neslihan KARACA

Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı Ve Hastalıkları Anabilim Dalı

Araştırma alanları: Sağlık Bilimleri, Tıp, Dahili Tıp Bilimleri, Pediatrik İmmünoloji ve Allerji, Çocuk Sağlığı ve Hastalıkları, Diğer, Tıbbi Genetik, Yaşam Bilimleri, Temel Bilimler, Temel Tıp Bilimleri

Yayınlar

B cells, autoimmunity, and innate immunity in 22q11.2 deletion syndrome: a two-center study and review of the literature (2026)
Jacquet Erosive Dermatitis in a Child with DOCK8 Mutation (2026)
Unclassified Inborn Errors of Immunity Patients without any Pathogenic Variant in Targeted Next-Generation Sequencing: Long-Term Follow-up and Whole Exome Sequencing Results (2026)
Tümör İmmünolojisi (2025)
Exploring the role of NOD2 variants in pediatric undifferentiated recurrent fever: a clinical and functional perspective (2025)
Monocyte plasticity and HLA-DR expression in patients with X-linked agammaglobulinemia (2025)
Self-reported Clinical Outcomes and Quality of Life in Agammaglobulinemia: the Importance of an Early Diagnosis (2025)
Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registry (2025)
Expansion of Myeloid-Derived Suppressor Cells and Lymphocyte Apoptosis Beyond B-Cell Deficiency in X-Linked Agammaglobulinemia (2025)
Correction to: Self-reported Clinical Outcomes and Quality of Life in Agammaglobulinemia: the Importance of an Early Diagnosis (2025)
Clinical and molecular findings in actin-related inborn errors of immunity: the middle East and North Africa registry (2025)
Self-reported Clinical Outcomes and Quality of Life in Agammaglobulinemia: the Importance of an Early Diagnosis (2025)
Expansion of Myeloid‐Derived Suppressor Cells and Lymphocyte Apoptosis Beyond B‐Cell Deficiency in X‐Linked Agammaglobulinemia (2025)
Exploring the role of NOD2 variants in pediatric undifferentiated recurrent fever: a clinical and functional perspective (2025)
Transient hypogammaglobulinemia of infancy and unclassified syndromic immunodeficiencies are highly common in oesophageal atresia patients (2024)
Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variants (2024)
MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort (2024)
Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients (2024)
Günümüzde İmmünoglobulin Tedavisinde neredeyiz ve Gelecekte beklentiler (2024)
Facilitated Subcutaneous Immunoglobulin Treatment Increases the Quality of Life and Decreases the Number of Infections and Hospitalizations in Children with Primary Immunodeficiencies (2024)
Immunological Defense Mechanisms of the Respiratory System (2024)
Wiskott-Aldrich syndrome: a study of 577 patients defines the genotype as a biomarker for disease severity and survival (2024)
Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients (2024)
Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis (2024)
Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients (2024)
Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experience (2023)
An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission (2023)
Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency (2023)
Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature (2023)
Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis (2023)
Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis (2023)
Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experience (2023)
Transient hypogammaglobulinemia of infancy: Clinical and immunologic features of 385 cases. (2023)
Yaygın Değişken İmmün Yetmezlikte Tanımlanan Genetik Defektler (2023)
Dual Diagnosis of Trichohepatoenteric Syndrome and Lipoid Proteinosis in a Turkish Child (2023)
Atypical Localization of Eczema Discriminates DOCK8 or STAT3 Deficiencies from Atopic Dermatitis (2023)
Novel immunodeficiency caused by homozygous mutation in SLC19A1 encoding the reduced folate carrier (2023)
Alterations in B and NK cells highly correlate with disease severity in children with COVID-19 (2023)
Autoimmune Cytopenias Are Highly Associated with Inborn Errors of Immunity and They May Be the Initial Presentations in Cases without Severe Infections (2023)
Current Genetic Defects in Common Variable Immune Deficiency Patients on the Geography Between Europe and Asia (2023)
Analysis of IL-1β, TGF- Β, Il-5, ACE and PTPN22 Gene Polymorphisms and GEN Expression Levels in Turkish Chlidren with IgA Vasculitis (2023)
Mid-Regional Proadrenomedullin Levels in Primary Immunodeficiencies Complicated with Pulmonary Manifestations (2022)
iMMÜNOLOJÍ Antikor Eksikliğine Bağlı Primer İmmün Yetmezlikler (2022)
A Remarkable Case of Autoimmune Polyendocrinopathy, Candidiasis and Ectodermal Dystrophy Syndrome (APECED) misdiagnosed as Juvenile Idiopathic Arthritis on admission (2022)
COMBINED IMMUNODEFICIENCY DUE TO JAK3 MUTATION ASSOCIATED WITH REFRACTORY CMV INFECTION AND BCG-OSİ (2022)
Psödomanas Aeruginosa Kolonize Kistik Fibrozisli Hastaların Nötrofil Fonksiyonlarının Değerlendirilmesi (2022)
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 (2022)
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 (2022)
Atypical STAT5B deficiency, severe short stature and mild immunodeficiency associated with a novel homozygous STAT5B Variant (2022)
Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry (2022)
Regulatory B cells in patients suffering from inborn errors of immunity with severe immune dysregulation (2022)
Comparing the levels of CTLA‐4‐dependent biological defects in patients with LRBA deficiency and CTLA‐4 insufficiency (2022)
Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants (2022)
X-linked agammaglobulinemia: investigation of clinical and laboratory findings, novel gene mutations and prevention of infective complications in long-term follow-up (2021)
X-linked agammaglobulinemia: investigation of clinical and laboratory findings, novel gene mutations and prevention of infective complications in long-term follow-up (vol 10, pg 37, 2021) (2021)
Combined immunodeficiency with marginal zone lymphoma due to a novel homozygous mutation inIL-21Rgene and successful treatment with hematopoietic stem cell transplantation (2021)
Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA-2; PLCG2): Striking clinical phenotypic overlap and difference (2021)
Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature (2021)
COVID19 pandemisinin primer immün yetmezlik tanılı hastalar üzerinde etkisi (2021)
Erratum: X-linked agammaglobulinemia: investigation of clinical and laboratory findings, novel gene mutations and prevention of infective complications in long-term follow-up. (2021)
IRF9 Eksikliği, Viral Enfeksiyona Duyarlılık, Maligniteye Eğilim (2021)
Neutropenia in Primary Immunodeficiency Diseases (2021)
A Novel Homozygous TRNT1 Mutation in a Child with an Early Diagnosis of Common Variable Immunodeficiency Leading to Mild Hypogammaglobulinemia and Hemolytic Anemia (2021)
Combined immunodeficiency with marginal zone lymphoma due to a novel homozygous mutation in IL-21R gene and successful treatment with hematopoietic stem cell transplantation (2021)
X-linked agammaglobulinemia: investigation of clinical and laboratory findings, novel gene mutations and prevention of infective complications in long-term follow-up (2021)
X-linked agammaglobulinemia: ınvestigation of clinical and laboratory findings, novel gene mutations and prevention of ınfective complications in long-term follow-up. (2021)
Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA-2; PLCG2 ): striking clinical phenotypic overlap and difference (2021)
Consensus Middle East and North Africa Registry on Inborn Errors of Immunity (2021)
X-linked agammaglobulinemia: ınvestigation of clinical and laboratory findings, novel gene mutations and prevention of ınfective complications in long-term follow-up (2021)
X-linked agammaglobulinemia: ınvestigation of clinical and laboratory findings, novel gene mutations and prevention of ınfective complications in long-term follow-up (2021)
Common variable immunodeficiency: familial inheritance and autoimmune manifestations in two siblings (2021)
A Novel Homozygous TRNT1 Mutation in a Child With an Early Diagnosis of Common Variable Immunodeficiency Leading to Mild Hypogammaglobulinemia and Hemolytic Anemia. (2021)
X-linked agammaglobulinemia: ınvestigation of clinical and laboratory findings, novel gene mutations and prevention of ınfective complications in long-term follow-up. (2021)
22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease management (2021)
Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant (2021)
Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature (2021)
International Survey And Retrospective Analysis of 28 Patients With IFN-Gamma-Receptor Deficiency (2021)
LRBA VE CTLA-4 EKSIKLIĞI OLGULARINDA SOLUBLECD25 VE FOLIKÜLER T HÜCRE DÜZEYLERI HASTALIK AKTIVITESINI GÖSTERMEDE BAŞARILIDIR. (2020)
A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature (2020)
Autoantibody Positivity in Children with Chronic Diarrhea (2020)
The evaluation of malignancies in Turkish primary immunodeficiency patients a multicenter study (2020)
Autoantibody Positivity in Children with Chronic Diarrhea (2020)
Primer İmmün Yetersizlik Şüphesi OlanHastaya Yaklaşım Nasıl Olmalıdır? (2020)
Efficacy and quality of life assessment in the use of subcutaneous immunoglobulin treatment in children with primary immunodeficiency (2020)
LBRA VE CTLA-4 EKSIKLIKLERININ TANISINDA VE AYRIMINDA KLINIK OZELLIKLERIN VE IMMUNOLOJIK TESTLERIN DEĞERI. (2020)
ÇOCUK ROMATOLOJİ HASTALARINDA HASTANE MALNÜTRİSYONU VE MALNÜTRİSYON SKORLAMALARI (2020)
Romatoloji hastalarında hastane malnütrisyonu ve malnütrisyon skorları. (2020)
The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study (2020)
A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature (2020)
. IL21R defektine bağlı kombine immün yetmezlik zemininde gelişen marjinal zone lenfomalı olgu. (2019)
İnterlökin 12 / Interferon gamma yolak bozuklukları ve atipik mikobakteriyel enfeksiyonlara yatkınlık (2019)
İmmün yetmezliklerde Tedavide Yenilikler (2019)
Genetically defined mutations in primary immunodeficiencies by new generation sequencing targeted gene method: results of 200 patients from one center in Western Turkey (2019)
Hematopoietic stem cell transplantation in pediatric DOCK8 deficiency related hiper ige syndrome (2019)
Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages (2019)
A Novel TTC37 Mutation Causing Clinical Symptoms of Trichohepatoenteric Syndrome Such as Pyoderma Gangrenosum and Immunodeficiency Without Severe Diarrhea (2019)
Antı-β2 Glycoprotein I Antibodies in Children with Rheumatologic Disorders (2019)
Chapter 65. Constrictive Aspergillosis Pericarditis (2019)
Chapter 95. Early-Onset Inflammatory Bowel DiseaseNeslihan Edeer Karaca, Guzide Aksu, and Necil Kutukculer (2019)
Chapter 143. BCGosis and Hyperferritinemia (2019)

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