Vera Goda

Pest, BU, Hungary

Last Updated: 09/26/2026

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Found 17 publications

Phenocopies of 22q11.2DS: revealing genetic diversity in clinically suspected 22q11.2 deletion syndrome.

Phenocopies of 22q11.2DS: revealing genetic diversity in clinically suspected 22q11.2 deletion syndrome.

Journal: Molecular and cellular pediatrics
Published: November 25, 2025

Identification of genetically determined chronic childhood cytopenia in the era of molecular medicine

Identification of genetically determined chronic childhood cytopenia in the era of molecular medicine

Journal: Orvosi hetilap
Published: September 27, 2024

Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.

Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity.

Journal: The Journal of allergy and clinical immunology
Published: April 08, 2023

Bone Turnover Marker for the Evaluation of Skeletal Remodelling in Autosomal Recessive Osteopetrosis after Haematopoietic Stem Cell Transplantation: A Case Report.

Bone Turnover Marker for the Evaluation of Skeletal Remodelling in Autosomal Recessive Osteopetrosis after Haematopoietic Stem Cell Transplantation: A Case Report.

Journal: Children (Basel, Switzerland)
Published: March 09, 2023

Reducing the risk of infections in hereditary and acquired complement deficiencies.

Reducing the risk of infections in hereditary and acquired complement deficiencies.

Journal: Orvosi hetilap
Published: March 07, 2023

Peripheral Bone Relapse of Paediatric TCF3-HLF Positive Acute Lymphoblastic Leukaemia during Haematopoietic Stem Cell Transplantation: A Case Report.

Peripheral Bone Relapse of Paediatric TCF3-HLF Positive Acute Lymphoblastic Leukaemia during Haematopoietic Stem Cell Transplantation: A Case Report.

Journal: Children (Basel, Switzerland)
Published: November 10, 2022

Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021.

Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021.

Journal: Frontiers in immunology
Published: August 30, 2022

Specific Antibody and the T-Cell Response Elicited by BNT162b2 Boosting After Two ChAdOx1 nCoV-19 in Common Variable Immunodeficiency.

Specific Antibody and the T-Cell Response Elicited by BNT162b2 Boosting After Two ChAdOx1 nCoV-19 in Common Variable Immunodeficiency.

Journal: Frontiers in immunology
Published: March 29, 2022

Author Correction: Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice.

Author Correction: Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice.

Journal: Nature genetics
Published: January 06, 2022

Multicenter Experience of Hematopoietic Stem Cell Transplantation in WHIM Syndrome.

Multicenter Experience of Hematopoietic Stem Cell Transplantation in WHIM Syndrome.

Journal: Journal of clinical immunology
Published: April 08, 2021

Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients.

Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients.

Journal: Journal of clinical immunology
Published: January 25, 2021

Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice.

Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice.

Journal: Nature genetics
Published: April 25, 2020
Showing 1-12 of 17

Last Updated: 09/26/2026