SK
S Kostel Bal
Also known as: Sevgi Köstel Bal, Sevgi Köstel, Ayşe Sevgi Köstel, Ayşe Sevgi Köstel Bal
St. Anna Children's Cancer Research Institute
Research areas: Immunology and Microbiology · Immunology · Immunodeficiency and Autoimmune Disorders · Blood disorders and treatments · T-cell and B-cell Immunology
0000-0002-3718-5323
Employment
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (51)
- Nuclear Factor Kappa B (NF‐κB)1 and NF‐κB2 Deficiency: An Unpredictable Defect With Wide Clinical and Immunologic Phenotype Save
- Clinical spectrum and survival outcomes of malignancies in pediatric patients with inborn errors of immunity Save
- Clinical, immunological, treatment characteristics, and outcomes in 22 patients with major histocompatibility complex class II deficiency Save
- Acute Generalized Exanthematous Pustulosis in Pediatric Patients: A Rare Drug Reaction from the Neonatal to Adolescent Period Save
- Clinical and immunological spectrum of MHC class I deficiency: insights from a long-term cohort with two novel mutations Save
- Evaluation of Patients with Combined Immunodeficiency: A Single Center Experience Save
- Long-term outcome of bone marrow transplantation in NIK deficiency: non-redundant role of non-canonical NF-κB signaling in thymic reconstitution and secondary lymphoid organ development Save
- Next Generation Sequencing Based Gene Identification Techniques as a Diagnostic Approach For Patients with the CVID Phenotype Save
- LTβR deficiency causes lymph node aplasia and impaired B cell differentiation Save
- Rapamycin Controls Lymphoproliferation and Reverses T-Cell Responses in a Patient with a Novel STIM1 Loss-of-Function Deletion Save
- A Novel Homozygous Six Base Pair Deletion Found in the NFATC2 Gene in a Patient with EBV-Associated Lymphoproliferation Save
- Extended Phenotype of VPS45 Defect with Additional Features of Combined Immunodeficiency and Neuromotor Developmental Delay Along with Severe Congenital Neutropenia Save
- AutoCore: A network-based definition of the core module of human autoimmunity and autoinflammation Save
- Systemic Inflammation and Normocytic Anemia in DOCK11 Deficiency Save
- Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis. Save
- Evaluation of thymopoiesis in healthy Turkish children aged 0-6 years. Save
- Alterations in insulin-like growth factor system in spinal muscular atrophy. Save
- Identification of germline monoallelic mutations in IKZF2 in patients with immune dysregulation. Save
- Biallelic germline mutation in IKZF2, encoding Helios, causes pleiotropic defects of immunity Save
- Curation and Expansion of Human Phenotype Ontology for Inborn Errors of Immunity Save