Luis E. Solano-Becerra

Guadalajara, JAL, Mexico

Last Updated: 09/26/2026

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Found 15 publications

Recommendations for genetic counseling for individuals at risk of autosomal dominant Alzheimer's disease in Latin America.

Recommendations for genetic counseling for individuals at risk of autosomal dominant Alzheimer's disease in Latin America.

Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association

Published: February 12, 2026

Primary Progressive Aphasias: Diagnosis and Treatment.

Primary Progressive Aphasias: Diagnosis and Treatment.

Journal: Brain sciences

Published: January 03, 2025

Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis.

Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis.

Journal: Genetic testing and molecular biomarkers

Published: May 31, 2022

Study of the Interaction of Ti-Zn as a Mixed Oxide at Different pH Values Synthesized by the Sol-Gel Method and Its Antibacterial Properties.

Study of the Interaction of Ti-Zn as a Mixed Oxide at Different pH Values Synthesized by the Sol-Gel Method and Its Antibacterial Properties.

Journal: Nanomaterials (Basel, Switzerland)

Published: May 05, 2022

A Study of Zn-Ca Nanocomposites and Their Antibacterial Properties.

A Study of Zn-Ca Nanocomposites and Their Antibacterial Properties.

Journal: International journal of molecular sciences

Published: April 30, 2022

Clinical Exome Sequencing Enables Congenital Sialidosis Type II Diagnosis in Two Siblings Presenting with Unreported Clinical Features from a Rare Homozygous Sequence Variant p.(Tyr370Cys) in NEU1.

Clinical Exome Sequencing Enables Congenital Sialidosis Type II Diagnosis in Two Siblings Presenting with Unreported Clinical Features from a Rare Homozygous Sequence Variant p.(Tyr370Cys) in NEU1.

Journal: Molecular syndromology

Published: November 18, 2020

Microcephaly, an etiopathogenic vision.

Microcephaly, an etiopathogenic vision.

Journal: Pediatrics and neonatology

Published: November 04, 2020

Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositis.

Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositis.

Journal: Autoimmunity

Published: June 30, 2020

Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder.

Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder.

Journal: Journal of autism and developmental disorders

Published: March 04, 2019

PEDIA: prioritization of exome data by image analysis.

PEDIA: prioritization of exome data by image analysis.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 13, 2018

Severe Craniofacial Involvement due to Amniotic Band Sequence.

Severe Craniofacial Involvement due to Amniotic Band Sequence.

Journal: Fetal and pediatric pathology

Published: January 17, 2018

An update on amniotic bands sequence.

An update on amniotic bands sequence.

Journal: Archivos argentinos de pediatria

Published: July 06, 2017

Showing 1-12 of 15

Last Updated: 09/26/2026