Adriana Ochoa
Mexico City, DIF, Mexico
Last Updated: 09/26/2026
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Found 9 publications
Increased non-attendance at epilepsy clinic in patients with neuropsychiatric comorbidities: A prospective study.
Journal: Epilepsy & behavior : E&B
Published: May 21, 2021
Association of polymorphisms and reduced expression levels of the NR4A2 gene with Parkinson's disease in a Mexican population.
Journal: Journal of the neurological sciences
Published: December 06, 2016
High-dose versus low-dose valproate for the treatment of juvenile myoclonic epilepsy: Going from low to high.
Journal: Epilepsy & behavior : E&B
Published: January 19, 2016
EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 23, 2015
Chromosome loci vary by juvenile myoclonic epilepsy subsyndromes: linkage and haplotype analysis applied to epilepsy and EEG 3.5-6.0 Hz polyspike waves.
Journal: Molecular genetics & genomic medicine
Published: July 23, 2015
CYP2D6 genetic polymorphisms in Southern Mexican Mayan Lacandones and Mestizos from Chiapas.
Journal: Pharmacogenomics
Published: December 16, 2014
Late onset Lafora disease and novel EPM2A mutations: breaking paradigms.
Journal: Epilepsy research
Published: April 10, 2014
Absence of Multiple Sclerosis and Demyelinating Diseases among Lacandonians, a Pure Amerindian Ethnic Group in Mexico.
Journal: Multiple sclerosis international
Published: June 05, 2012
Novel Myoclonin1/EFHC1 mutations in Mexican patients with juvenile myoclonic epilepsy.
Journal: Seizure
Published: February 01, 2012
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Last Updated: 09/26/2026