Rebeca Pena-Rodriguez

La Paz, MD, Spain

Last Updated: 09/26/2026

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Found 31 publications

Immune and vascular dysregulation at the maternal-fetal interface in oocyte donation triplet pregnancies: unraveling mechanisms of failed immune tolerance.

Immune and vascular dysregulation at the maternal-fetal interface in oocyte donation triplet pregnancies: unraveling mechanisms of failed immune tolerance.

Journal: Placenta

Published: August 11, 2025

Infectious and inflammatory events in 2 siblings with IRF9 deficiency under immunoglobulin replacement therapy.

Infectious and inflammatory events in 2 siblings with IRF9 deficiency under immunoglobulin replacement therapy.

Journal: The Journal of allergy and clinical immunology

Published: May 21, 2025

Functional insights of an uncommon hypomorphic variant in IL2RG as a monogenic cause of CVID-like disease with antibody deficiency and T CD4 lymphopenia.

Functional insights of an uncommon hypomorphic variant in IL2RG as a monogenic cause of CVID-like disease with antibody deficiency and T CD4 lymphopenia.

Journal: Frontiers in immunology

Published: December 13, 2024

Novel NFKBIA variant causing autosomal ectodermal dysplasia with immunodeficiency.

Novel NFKBIA variant causing autosomal ectodermal dysplasia with immunodeficiency.

Journal: Journal of the European Academy of Dermatology and Venereology : JEADV

Published: October 14, 2024

Molecular assessment of splicing variants in a cohort of patients with inborn errors of immunity: methodological approach and interpretation remarks.

Molecular assessment of splicing variants in a cohort of patients with inborn errors of immunity: methodological approach and interpretation remarks.

Journal: Frontiers in immunology

Published: September 20, 2024

Technical challenges of intracellular flow cytometry-based assays as a functional complement to diagnosis of signaling defects of inborn errors of immunity: PI3K pathway as a case of study.

Technical challenges of intracellular flow cytometry-based assays as a functional complement to diagnosis of signaling defects of inborn errors of immunity: PI3K pathway as a case of study.

Journal: Frontiers in immunology

Published: August 05, 2024

Novel hypomorphic CYBB variant causing chronic granulomatous disease with incomplete penetrance.

Novel hypomorphic CYBB variant causing chronic granulomatous disease with incomplete penetrance.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Published: July 25, 2024

Detection of specific RBD+ IgG+ memory B cells by flow cytometry in healthcare workers and patients with inborn errors of immunity after BNT162b2 m RNA COVID-19 vaccination.

Detection of specific RBD+ IgG+ memory B cells by flow cytometry in healthcare workers and patients with inborn errors of immunity after BNT162b2 m RNA COVID-19 vaccination.

Journal: Frontiers in immunology

Published: January 02, 2023

Research-based flow cytometry assays for pathogenic assessment in the human B-cell biology of gene variants revealed in the diagnosis of inborn errors of immunity: a Bruton's tyrosine kinase case-study.

Research-based flow cytometry assays for pathogenic assessment in the human B-cell biology of gene variants revealed in the diagnosis of inborn errors of immunity: a Bruton's tyrosine kinase case-study.

Journal: Frontiers in immunology

Published: November 10, 2022

Variants in CASP10, a diagnostic challenge: Single center experience and review of the literature.

Variants in CASP10, a diagnostic challenge: Single center experience and review of the literature.

Journal: Clinical immunology (Orlando, Fla.)

Published: May 14, 2021

Primary Immune Regulatory Disorders With an Autoimmune Lymphoproliferative Syndrome-Like Phenotype: Immunologic Evaluation, Early Diagnosis and Management.

Primary Immune Regulatory Disorders With an Autoimmune Lymphoproliferative Syndrome-Like Phenotype: Immunologic Evaluation, Early Diagnosis and Management.

Journal: Frontiers in immunology

Published: February 24, 2021

Next Generation Sequencing for Detecting Somatic FAS Mutations in Patients With Autoimmune Lymphoproliferative Syndrome.

Next Generation Sequencing for Detecting Somatic FAS Mutations in Patients With Autoimmune Lymphoproliferative Syndrome.

Journal: Frontiers in immunology

Published: January 20, 2021

Showing 1-12 of 31

Last Updated: 09/26/2026