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Pharmacogenomics|December 16, 2014
HLA-A*02:01:01/-B*35:01:01/-C*04:01:01 haplotype associated with lamotrigine-induced maculopapular exanthema in Mexican Mestizo patientsIngrid Fricke-Galindo, Iris E Martínez-Juárez, Nancy Monroy-Jaramillo, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|May 3, 2018
Phenotypic Variability in a Mexican Mestizo Family with Retinal Vasculopathy with Cerebral Leukodystrophy and TREX1 Mutation p.V235Gfs*6Nancy Monroy-Jaramillo, Aurelio Cerón, Elizabeth León, et al.
Epilepsy Research|September 24, 2014
Late onset Lafora disease and novel EPM2A mutations: breaking paradigmsAurelio Jara-Prado, Adriana Ochoa, María Elisa Alonso, et al.
Seizure|June 26, 2012
Novel Myoclonin1/EFHC1 mutations in Mexican patients with juvenile myoclonic epilepsyAurelio Jara-Prado, Iris E Martínez-Juárez, Adriana Ochoa, et al.
Journal of the Neurological Sciences|March 6, 2016
Synaptotagmin XI in Parkinson's disease: New evidence from an association study in Spain and MexicoAngel Sesar, Pilar Cacheiro, Marisol López-López, et al.
Brain : a Journal of Neurology|March 8, 2006
Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-upIris E Martínez-Juárez, María Elisa Alonso, Marco T Medina, et al.
Epilepsia|November 24, 2005
Seizures of idiopathic generalized epilepsiesReyna M Durón, Marco T Medina, Iris E Martínez-Juárez, et al.
Annals of Neurology|April 5, 2016
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseasesConceição Bettencourt, Davina Hensman-Moss, Michael Flower, et al.
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