Jaime A. Valdez-Lopez

San Miguel, AGU, Mexico

Last Updated: 09/26/2026

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Found 12 publications

Placental Methylation Profile in Women Exposed to Fluoride and Its Association with Kidney Volume at Birth.

Placental Methylation Profile in Women Exposed to Fluoride and Its Association with Kidney Volume at Birth.

Journal: Clinical journal of the American Society of Nephrology : CJASN

Published: December 10, 2025

A Retrospective Study of Clinical and Genetic Features in a Long-Term Cohort of Mexican Children with Alagille Syndrome.

A Retrospective Study of Clinical and Genetic Features in a Long-Term Cohort of Mexican Children with Alagille Syndrome.

Journal: International journal of molecular sciences

Published: June 07, 2025

Chromosome analysis of 303 pregnancy losses in Mexico.

Chromosome analysis of 303 pregnancy losses in Mexico.

Journal: Gaceta medica de Mexico

Published: May 16, 2024

Mutational spectrum and genotype-phenotype correlation in Mexican patients with infantile-onset and late-onset Pompe disease.

Mutational spectrum and genotype-phenotype correlation in Mexican patients with infantile-onset and late-onset Pompe disease.

Journal: Molecular genetics & genomic medicine

Published: December 04, 2023

Myosin 1g as a high-risk biomarker in a pediatric patient with lineage switch from acute lymphoblastic leukemia to myeloid phenotype.

Myosin 1g as a high-risk biomarker in a pediatric patient with lineage switch from acute lymphoblastic leukemia to myeloid phenotype.

Journal: Boletin medico del Hospital Infantil de Mexico

Published: May 08, 2023

Infantile-onset Pompe disease in seven Mexican children.

Infantile-onset Pompe disease in seven Mexican children.

Journal: Gaceta medica de Mexico

Published: December 26, 2022

Cystic fibrosis: current concepts.

Cystic fibrosis: current concepts.

Journal: Boletin medico del Hospital Infantil de Mexico

Published: December 22, 2021

Hawkinsinuria clinical practice guidelines: a Mexican case report and literature review.

Hawkinsinuria clinical practice guidelines: a Mexican case report and literature review.

Journal: The Journal of international medical research

Published: July 26, 2019

Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations.

Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations.

Journal: Human genetics

Published: August 24, 2018

Primary Immunodeficiency Diseases in Aguascalientes, Mexico: Results from an Educational Program.

Primary Immunodeficiency Diseases in Aguascalientes, Mexico: Results from an Educational Program.

Journal: Journal of clinical immunology

Published: September 09, 2014

ATP6V0A2 mutations present in two Mexican Mestizo children with an autosomal recessive cutis laxa syndrome type IIA.

ATP6V0A2 mutations present in two Mexican Mestizo children with an autosomal recessive cutis laxa syndrome type IIA.

Journal: Molecular genetics and metabolism reports

Published: March 10, 2014

A fetus with hemifacial microsomia and sirenomelia. The same mesodermal defect spectrum?

A fetus with hemifacial microsomia and sirenomelia. The same mesodermal defect spectrum?

Journal: Fetal and pediatric pathology

Published: May 31, 2012

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Last Updated: 09/26/2026