Maria I. Ramos-Mendoza

Tlalnepantla, MOR 54090, Mexico

Last Updated: 09/26/2026

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Found 10 publications

Genetic and Molecular Characterization of Treacher Collins Syndrome in Three Mexican Families.

Genetic and Molecular Characterization of Treacher Collins Syndrome in Three Mexican Families.

Journal: International journal of molecular sciences

Published: December 31, 2025

Distinct Immunophenotypes in the DNA Index-Based Stratification of Pediatric B-Cell Acute Lymphoblastic Leukemia.

Distinct Immunophenotypes in the DNA Index-Based Stratification of Pediatric B-Cell Acute Lymphoblastic Leukemia.

Journal: Cancers

Published: September 09, 2024

Prevalence of sexually risky behaviors among Mexican medical students.

Prevalence of sexually risky behaviors among Mexican medical students.

Journal: PloS one

Published: October 10, 2023

Identification of Compound Heterozygous EVC2 Gene Variants in Two Mexican Families with Ellis-van Creveld Syndrome.

Identification of Compound Heterozygous EVC2 Gene Variants in Two Mexican Families with Ellis-van Creveld Syndrome.

Journal: Genes

Published: January 16, 2023

Antifungal Activity of Mexican Propolis on Clinical Isolates of Candida Species.

Antifungal Activity of Mexican Propolis on Clinical Isolates of Candida Species.

Journal: Molecules (Basel, Switzerland)

Published: August 03, 2022

Human papillomavirus infection and seroprevalence among female university students in Mexico.

Human papillomavirus infection and seroprevalence among female university students in Mexico.

Journal: Human vaccines & immunotherapeutics

Published: February 01, 2022

Flavonoids Present in Propolis in the Battle against Photoaging and Psoriasis.

Flavonoids Present in Propolis in the Battle against Photoaging and Psoriasis.

Journal: Antioxidants (Basel, Switzerland)

Published: November 13, 2021

Effects of Propolis on Infectious Diseases of Medical Relevance.

Effects of Propolis on Infectious Diseases of Medical Relevance.

Journal: Biology

Published: April 23, 2021

Hypohidrotic ectodermal dysplasia: clinical and molecular review.

Hypohidrotic ectodermal dysplasia: clinical and molecular review.

Journal: International journal of dermatology

Published: December 30, 2016

Novel missense mutation in the EDA1 gene identified in a family with hypohidrotic ectodermal dysplasia.

Novel missense mutation in the EDA1 gene identified in a family with hypohidrotic ectodermal dysplasia.

Journal: International journal of dermatology

Published: December 10, 2013

Showing 1-10 of 10

Last Updated: 09/26/2026