Publications by authors named "Maria Elisa Alonso"

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Late onset Lafora disease and novel EPM2A mutations: breaking paradigms.
Aurelio Jara-Prado, Adriana Ochoa, María Elisa Alonso, Gabriel A Lima Villeda, Francisca Fernández-Valverde

Epilepsy Res· November 2014

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Interethnic differences in UGT1A4 genetic polymorphisms between Mexican Mestizo and Spanish populations.
Marisol López, Pedro Dorado, Alberto Ortega, Eva Peñas-Lledó, Nancy Monroy, María Elisa Alonso

Mol Biol Rep· April 2013

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Novel Myoclonin1/EFHC1 mutations in Mexican patients with juvenile myoclonic epilepsy.
Aurelio Jara-Prado, Iris E Martínez-Juárez, Adriana Ochoa, Víctor M González, María Del Carmen Fernández-González-Aragón, María Elisa Alonso

Seizure· September 2012

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Pharmacogenetics of the antiepileptic drugs phenytoin and lamotrigine.
Marisol López, Pedro Dorado, Nancy Monroy, María Elisa Alonso, Helgi Jung-Cook

Drug Metabol Drug Interact· August 2012

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Low frequency of common LRRK2 mutations in Mexican patients with Parkinson's disease.
Petra Yescas, Marisol López, Nancy Monroy, Marie-Catherine Boll, Mayela Rodríguez-Violante, María Elisa Alonso

Neurosci Lett· November 2010

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Presymptomatic diagnosis in Huntington's disease: the Mexican experience.
Maria Elisa Alonso, Adriana Ochoa, Ana Luisa Sosa, Yaneth Rodríguez, Mireya Chávez

Genet Test Mol Biomarkers· December 2009

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Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy.
Miyabi Tanaka, Richard W Olsen, Marco T Medina, Emily Schwartz, Maria Elisa Alonso

Am J Hum Genet· June 2008

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Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17.
Astrid Rasmussen, Irene De Biase, Marcela Fragoso-Benítez, Marco Antonio Macías-Flores, Petra Yescas, María Elisa Alonso

Ann Neurol· June 2007

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Apolipoprotein E epsilon4 allele is associated with Parkinson disease risk in a Mexican Mestizo population.
Marisol López, Jorge Guerrero, Petra Yescas, Marie-Catherine Boll, Itziar Familiar, María Elisa Alonso

Mov Disord· February 2007

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Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families.
Petra Yescas, Adriana Huertas-Vazquez, María Teresa Villarreal-Molina, Astrid Rasmussen, María Teresa Tusié-Luna, María Elisa Alonso

Neurogenetics· July 2006

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Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
Iris E Martínez-Juárez, María Elisa Alonso, Marco T Medina, Reyna M Durón, Julia N Bailey

Brain· May 2006

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Seizures of idiopathic generalized epilepsies.
Reyna M Durón, Marco T Medina, Iris E Martínez-Juárez, Julia N Bailey, Katerina Tanya Perez-Gosiengfiao, María Elisa Alonso

Epilepsia· December 2005

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CYP2D6 genotype and phenotype determination in a Mexican Mestizo population.
Marisol López, Jorge Guerrero, Helgi Jung-Cook, María Elisa Alonso

Eur J Clin Pharmacol· November 2005

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Familial juvenile myoclonic epilepsy.
María Elisa Alonso, Marco T Medina, Iris E Martínez-Juárez, Reyna M Durón, Julia N Bailey

Adv Neurol· December 2004

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Recent developments in the quest for myoclonic epilepsy genes.
Antonio V Delgado-Escueta, Katerina B Perez-Gosiengfiao, Dongsheng Bai, Julia Bailey, Marco T Medina, Maria Elisa Alonso

Epilepsia· December 2003

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Olfactory dysfunction in hereditary ataxia and basal ganglia disorders.
Juan Fernandez-Ruiz, Rosalinda Díaz, Cynthia Hall-Haro, Patricia Vergara, Aldo Fiorentini, Maria-Elisa Alonso

Neuroreport· July 2003

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Genetics of idiopathic myoclonic epilepsies: an overview.
Antonio V Delgado-Escueta, Marco T Medina, Dong Sheng Bai, Chung Yan Fong, Miyabi Tanaka, Maria Elisa Alonso

Adv Neurol· October 2002

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