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Publications by Vilma Regina Martins

Creutzfeldt-Jakob Disease Associated With a Missense Mutation at Codon 200 of the Prion Protein Gene in Brazil

Dementia e Neuropsychologia

Sensory Systems

Cognitive Neuroscience

English

Related publications

Novel Prion Protein Gene Mutation in an Octogenarian With Creutzfeldt-Jakob Disease

Archives of Neurology

English

Accumulation of Prion Protein in the Vagus Nerve in Creutzfeldt-Jakob Disease

Annals of Neurology

English

Variant Creutzfeldt–Jakob Disease in a Patient With Heterozygosity at PRNP Codon 129

New England Journal of Medicine

English

Altered Prion Protein Expression Pattern in CSF as a Biomarker for Creutzfeldt-Jakob Disease

Multidisciplinary

English

Affected Siblings With Alzheimer's Disease Had Missense Mutation of Codon 717 in Amyloid Precursor Protein Gene.

Japanese Journal of Geriatrics

English

Erratum To: R208h-129vv Haplotype in the Prion Protein Gene: Phenotype and Neuroimaging of a Patient With Genetic Creutzfeldt-Jakob Disease

Journal of Neurology

English

Pathologic Prion Protein Spreading in the Peripheral Nervous System of a Patient With Sporadic Creutzfeldt-Jakob Disease

Archives of Neurology

English

Astrocyte Gene Expression in Creutzfeldt-Jakob Disease.

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Rare Genetic Creutzfeldt-Jakob Disease With E196A Mutation: A Case Report

Molecular Neuroscience

Infectious Diseases

English