Figen E. Dogu

Ankara, Turkey

Last Updated: 09/26/2026

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Found 99 publications

Clinical spectrum and survival outcomes of malignancies in pediatric patients with inborn errors of immunity.

Clinical spectrum and survival outcomes of malignancies in pediatric patients with inborn errors of immunity.

Journal: Frontiers in immunology

Published: June 09, 2026

A novel FLNA p.Pro2469Ser variant is associated with impaired T and NK cell function and immune dysregulation.

A novel FLNA p.Pro2469Ser variant is associated with impaired T and NK cell function and immune dysregulation.

Journal: Immunologic research

Published: May 14, 2026

A Rare Cause of Vesiculobullous Lesions in Childhood: 4 Cases of Cutaneous Mastocytosis.

A Rare Cause of Vesiculobullous Lesions in Childhood: 4 Cases of Cutaneous Mastocytosis.

Journal: Turkish archives of pediatrics

Published: May 05, 2026

Pneumococcal Serological Evaluation in Vaccinated Children Diagnosed with Transient Hypogammaglobulinemia of Infancy and Unclassified Hypogammaglobulinemia.

Pneumococcal Serological Evaluation in Vaccinated Children Diagnosed with Transient Hypogammaglobulinemia of Infancy and Unclassified Hypogammaglobulinemia.

Journal: International archives of allergy and immunology

Published: March 18, 2026

Delayed-Type Drug-Induced Cutaneous Adverse Reactions in Children: Clinical Spectrum, Diagnostic Challenges and Outcomes.

Delayed-Type Drug-Induced Cutaneous Adverse Reactions in Children: Clinical Spectrum, Diagnostic Challenges and Outcomes.

Journal: International archives of allergy and immunology

Published: March 06, 2026

Clinical, immunological, treatment characteristics, and outcomes in 22 patients with major histocompatibility complex class II deficiency.

Clinical, immunological, treatment characteristics, and outcomes in 22 patients with major histocompatibility complex class II deficiency.

Journal: Frontiers in immunology

Published: February 14, 2026

Primary Hemophagocytic Lymphohistiocytosis: A Severe Immune Dysregulatory Disease with Various Genotypic Features and Outcomes: A Cross-Sectional Study from a Tertiary Pediatric Center

Primary Hemophagocytic Lymphohistiocytosis: A Severe Immune Dysregulatory Disease with Various Genotypic Features and Outcomes: A Cross-Sectional Study from a Tertiary Pediatric Center

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: December 24, 2025

Nuclear Factor Kappa B (NF-κB)1 and NF-κB2 Deficiency: An Unpredictable Defect With Wide Clinical and Immunologic Phenotype.

Nuclear Factor Kappa B (NF-κB)1 and NF-κB2 Deficiency: An Unpredictable Defect With Wide Clinical and Immunologic Phenotype.

Journal: Scandinavian journal of immunology

Published: December 15, 2025

Hematopoietic Stem Cell Transplantation in Severe Combined Immunodeficiency at the Pediatric Intensive Care Unit: Case Series of 5 Severe Combined Immunodeficiency Patients.

Hematopoietic Stem Cell Transplantation in Severe Combined Immunodeficiency at the Pediatric Intensive Care Unit: Case Series of 5 Severe Combined Immunodeficiency Patients.

Journal: Turkish archives of pediatrics

Published: October 02, 2025

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.

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.

Journal: Frontiers in immunology

Published: August 09, 2025

Clinical and immunological spectrum of MHC class I deficiency: insights from a long-term cohort with two novel mutations.

Clinical and immunological spectrum of MHC class I deficiency: insights from a long-term cohort with two novel mutations.

Journal: Frontiers in immunology

Published: July 28, 2025

Hematopoietic stem cell transplantation for purine nucleoside phosphorylase deficiency: an EBMT-IEWP retrospective study.

Hematopoietic stem cell transplantation for purine nucleoside phosphorylase deficiency: an EBMT-IEWP retrospective study.

Journal: Blood

Published: April 29, 2025

Showing 1-12 of 99

Last Updated: 09/26/2026