Neslihan KARACA

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

Research areas: Medicine, Health Sciences, Internal Medicine Sciences, Child Health and Diseases, Pediatric Immunology and Allergy, Other, Medical Genetics, Life Sciences, Natural Sciences, Fundamental Medical Sciences

Publications

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)
Jacquet Erosive Dermatitis in a Child with DOCK8 Mutation (2026)
B cells, autoimmunity, and innate immunity in 22q11.2 deletion syndrome: a two-center study and review of the literature (2026)
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)
Tümör İmmünolojisi (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)
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)
Monocyte plasticity and HLA-DR expression in patients with X-linked agammaglobulinemia (2025)
Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis (2024)
Immunological Defense Mechanisms of the Respiratory System (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)
Investigation of Phagocyte Functions in Pseudomonas-Colonized Cystic Fibrosis Patients (2024)
Transient hypogammaglobulinemia of infancy and unclassified syndromic immunodeficiencies are highly common in oesophageal atresia 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)
Primary immune regulatory disorders (PIRD): expanding the mutation spectrum in Turkey and identification of sixteen novel variants (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)
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)
An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission (2023)
Transient hypogammaglobulinemia of infancy: Clinical and immunologic features of 385 cases. (2023)
Yaygın Değişken İmmün Yetmezlikte Tanımlanan Genetik Defektler (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)
Current genetic defects in common variable immunodeficiency patients on the geography between Europe and Asia: a single-center experience (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)
Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis (2023)
Autoimmune Cytopenias Are Highly Associated with Inborn Errors of Immunity and They May Be the Initial Presentations in Cases without Severe Infections (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)
A Remarkable Case of Autoimmune Polyendocrinopathy, Candidiasis and Ectodermal Dystrophy Syndrome (APECED) misdiagnosed as Juvenile Idiopathic Arthritis on admission (2022)
Mid-Regional Proadrenomedullin Levels in Primary Immunodeficiencies Complicated with Pulmonary Manifestations (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)
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)
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)
iMMÜNOLOJÍ Antikor Eksikliğine Bağlı Primer İmmün Yetmezlikler (2022)
Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants (2022)
IRF9 Eksikliği, Viral Enfeksiyona Duyarlılık, Maligniteye Eğilim (2021)
X-linked agammaglobulinemia: investigation of clinical and laboratory findings, novel gene mutations and prevention of infective 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)
Neutropenia in Primary Immunodeficiency Diseases (2021)
Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA-2; PLCG2 ): striking clinical phenotypic overlap and difference (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: 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)
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: 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)
X-linked agammaglobulinemia: ınvestigation of clinical and laboratory findings, novel gene mutations and prevention of ınfective complications in long-term follow-up. (2021)
Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature (2021)
Common variable immunodeficiency: familial inheritance and autoimmune manifestations in two siblings (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)
COVID19 pandemisinin primer immün yetmezlik tanılı hastalar üzerinde etkisi (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)
Combined immunodeficiency with marginal zone lymphoma due to a novel homozygous mutation inIL-21Rgene and successful treatment with hematopoietic stem cell transplantation (2021)
Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature (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)
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)
International Survey And Retrospective Analysis of 28 Patients With IFN-Gamma-Receptor Deficiency (2021)
Autoantibody Positivity in Children with Chronic Diarrhea (2020)
Primer İmmün Yetersizlik Şüphesi OlanHastaya Yaklaşım Nasıl Olmalıdır? (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)
LRBA VE CTLA-4 EKSIKLIĞI OLGULARINDA SOLUBLECD25 VE FOLIKÜLER T HÜCRE DÜZEYLERI HASTALIK AKTIVITESINI GÖSTERMEDE BAŞARILIDIR. (2020)
Efficacy and quality of life assessment in the use of subcutaneous immunoglobulin treatment in children with primary immunodeficiency (2020)
ÇOCUK ROMATOLOJİ HASTALARINDA HASTANE MALNÜTRİSYONU VE MALNÜTRİSYON SKORLAMALARI (2020)
Romatoloji hastalarında hastane malnütrisyonu ve malnütrisyon skorları. (2020)
LBRA VE CTLA-4 EKSIKLIKLERININ TANISINDA VE AYRIMINDA KLINIK OZELLIKLERIN VE IMMUNOLOJIK TESTLERIN DEĞERI. (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)
The evaluation of malignancies in Turkish primary immunodeficiency patients; a multicenter study (2020)
Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages (2019)
Genetically defined mutations in primary immunodeficiencies by new generation sequencing targetted method: Results of 200 patients from one center in western Turkey (2019)
Ağır Kombine ve Kombine İmmun Yetmezliklerde Dirençli CMV enfeksiyonu: RAG1, ZAP70 Ve ORAI1 mutasyonları. (2019)
Konjenital hemolitik anemi ve hipogammaglobulinemi ile prezente olan TRNT1 hastalığı (2019)
TRNT1 disease presenting with congenital hemolytic anemia and hypogammoglobulinemia (2019)
Di George Sendromu Tanılı Olgularımızın Klinik Özellikleri ve İzlemleri (2019)
Ataksi-telenjiektazi tanılı hastaların retrospektif olarak incelenmesi: İki merkez deneyimi. (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)