Laura E. Garza-Martinez
Cp 64460
Monterrey, NLE 64460, Mexico
Monterrey, NLE 64460, Mexico
Last Updated: 09/26/2026
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Found 13 publications
Hereditary Spastic Paraplegia Type 83 with Homozygous Variant in HPDL, Report of 3 Cases in a Mexican Family.
Journal: Movement disorders clinical practice
Published: January 16, 2025
Prevalence of Glucose-6-Phosphate Dehydrogenase Deficiency in Newborns in Northeast Mexico.
Journal: American journal of perinatology
Published: August 17, 2022
Correlation Between CD133+ Stem Cells and Clinical Improvement in Patients with Autism Spectrum Disorders Treated with Intrathecal Bone Marrow-derived Mononuclear Cells.
Journal: Innovations in clinical neuroscience
Published: August 12, 2022
Serum biomarkers and Doppler pulsatile index increases likelihood ratio for prediction of preeclampsia in the second trimester of pregnancy.
Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: February 21, 2022
Molecular Characterization of Associated Pathogens in Febrile Patients during Inter-Epidemic Periods of Urban Arboviral Diseases in Tapachula Southern Mexico.
Journal: Pathogens (Basel, Switzerland)
Published: October 08, 2021
Bilateral plantar plaques in a patient with Keratitis-ichthyosis-deafness syndrome.
Journal: The Australasian journal of dermatology
Published: May 12, 2020
Genetic Variants at the rs4720169 Locus of TBX20 and the rs12921862 Locus of AXIN1 May Increase the Risk of Congenital Heart Defects in the Mexican Population: A Pilot Study.
Journal: Genetic testing and molecular biomarkers
Published: September 17, 2019
Association study in Mexican patients with thyrotoxic hypokalemic periodic paralysis.
Journal: Biomedical reports
Published: October 22, 2018
Phenotypic Variation in Patients with Homozygous c.1678G>T Mutation in EVC Gene: Report of Two Mexican Families with Ellis-van Creveld Syndrome.
Journal: The American journal of case reports
Published: December 13, 2017
Genetic variants in KCNJ11, TCF7L2 and HNF4A are associated with type 2 diabetes, BMI and dyslipidemia in families of Northeastern Mexico: A pilot study.
Journal: Experimental and therapeutic medicine
Published: June 18, 2015
Candidate gene polymorphisms and risk of psoriasis: A pilot study.
Journal: Experimental and therapeutic medicine
Published: November 03, 2014
An investigation into the MMP1 gene promoter region polymorphism--1607 2G with recessive dystrophic epidermolysis bullosa disease severity in northeastern Mexican patients.
Journal: International journal of dermatology
Published: June 06, 2014
Last Updated: 09/26/2026