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Rasmussen, Astrid
One or more keywords matched the following items that are connected to Rasmussen, Astrid
Item TypeName
Concept Mexico
Academic Article Clinical heterogeneity of recessive ataxia in the Mexican population.
Academic Article Clinical and molecular features of familial and sporadic cases of von Hippel-Lindau disease from Mexico.
Academic Article Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma.
Academic Article Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families.
Academic Article Apolipoprotein E epsilon4 allele is associated with Parkinson disease risk in a Mexican Mestizo population.
Academic Article Genetic admixture of European FRDA genes is the cause of Friedreich ataxia in the Mexican population.
Academic Article Clinical and genetic characteristics of Mexican Huntington's disease patients.
Academic Article Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures.
Academic Article Juvenile myoclonic epilepsy: linkage to chromosome 6p12 in Mexico families.
Academic Article Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.
Academic Article Anticipation and intergenerational repeat instability in spinocerebellar ataxia type 17.
Academic Article Presymptomatic diagnosis in Huntington's disease: the Mexican experience.
Academic Article Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture.
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  • Mexico