Lizbeth Galicia-Blancas

Mexico City, DIF, Mexico

Last Updated: 09/26/2026

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Found 56 publications

Heterogeneous immune cell composition in patients with combined immunodeficiency.

Heterogeneous immune cell composition in patients with combined immunodeficiency.

Journal: Frontiers in immunology
Published: March 13, 2026

Neutralizing autoantibodies against IFN-α2 and IFN-ω in a boy with a heterozygous variant in the FOXN1 gene.

Neutralizing autoantibodies against IFN-α2 and IFN-ω in a boy with a heterozygous variant in the FOXN1 gene.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Published: November 06, 2025

Hemophagocytic lymphohistiocytosis in 60 Mexican children with chronic granulomatous disease.

Hemophagocytic lymphohistiocytosis in 60 Mexican children with chronic granulomatous disease.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Published: August 14, 2025

Molecular analysis and immunological characterization of a founder mutation causing ARPC1B deficiency.

Molecular analysis and immunological characterization of a founder mutation causing ARPC1B deficiency.

Journal: Genes and immunity
Published: April 15, 2025

Job's not done: BCG-itis as the first manifestation of hyper-IgE syndrome. A case report and review of the literature.

Job's not done: BCG-itis as the first manifestation of hyper-IgE syndrome. A case report and review of the literature.

Journal: Clinical immunology (Orlando, Fla.)
Published: April 11, 2025

Clinical features, genotypes, and geographic distribution of 238 Latin American CGD patients.

Clinical features, genotypes, and geographic distribution of 238 Latin American CGD patients.

Journal: Journal of human immunity
Published: March 29, 2025

Postinfectious manifestations in two pediatric female X-linked carriers of chronic granulomatous disease.

Postinfectious manifestations in two pediatric female X-linked carriers of chronic granulomatous disease.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Published: March 07, 2025

A patient with complete IFN-γR1 deficiency and tuberculosis resembling BCG disease.

A patient with complete IFN-γR1 deficiency and tuberculosis resembling BCG disease.

Journal: Journal of human immunity
Published: February 20, 2025

Characterization of the first patient with disseminated coccidioidomycosis and autosomal dominant STAT1 deficiency.

Characterization of the first patient with disseminated coccidioidomycosis and autosomal dominant STAT1 deficiency.

Journal: Journal of human immunity
Published: February 20, 2025

Description of invasive aspergillosis in Mexican patients with chronic granulomatous disease.

Description of invasive aspergillosis in Mexican patients with chronic granulomatous disease.

Journal: Journal of human immunity
Published: February 19, 2025

In-depth immune profiling of a patient with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2 caused by a novel mutation in ZBTB24.

In-depth immune profiling of a patient with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2 caused by a novel mutation in ZBTB24.

Journal: Clinical and experimental immunology
Published: September 30, 2024

Clinical and genetic description of patients with chronic granulomatous disease in a pediatric hospital

Clinical and genetic description of patients with chronic granulomatous disease in a pediatric hospital

Journal: Biomedica : revista del Instituto Nacional de Salud
Published: May 31, 2024
Showing 1-12 of 56

Last Updated: 09/26/2026