Adriana Ochoa

Mutations in EFHC1 cause juvenile myoclonic epilepsy

Toshimitsu Suzuki, Antonio V. Delgado‐Escueta, Kripamoy Aguan et al. · Nature Genetics · 2004 · 370 citations

Disease Gene Identification, Genetics, Neuroscience +1

Hyperglycosylation and Reduced GABA Currents of Mutated GABRB3 Polypeptide in Remitting Childhood Absence Epilepsy

Miyabi Tanaka, Richard W. Olsen, Marco T. Medina et al. · The American Journal of Human Genetics · 2008 · 192 citations · Full text

Mutated Gabrb3 Polypeptide, G Protein-coupled Receptor, Medicine +8

Assessment of the nutrition status of patients with Huntington's disease

Araceli Trejo, Rosa Marı́a Tarrats, Ma. Elisa Alonso et al. · Nutrition · 2004 · 156 citations

Nutrition, Body Composition, Health Sciences +9

Clinical and genetic analysis of 4 Mexican families with spinocerebellar ataxia type 10

Astrid Rasmussen, Tohru Matsuura, Luís Ruano et al. · Annals of Neurology · 2001 · 141 citations

Huntington Disease in Children: Genotype-Phenotype Correlation

Astrid Rasmussen, Rosario Márquez Macías, Petra Yescas et al. · Neuropediatrics · 2000 · 87 citations

Neurological Disorder, Corticobasal Degeneration, Genetics +16