Listar por autor "Capellari, Sabina"

Mostrando ítems 1-1 de 1

Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families

Sarapura-Castro, Elison; Cosentino, Carlos; Landman, Jonathan; Landman, Avi; Torres, Luis; Nuñez, Yesenia; Capellari, Sabina; Parchi, Piero; Cornejo-Olivas, Mario (Elsevier, 2021)

Highlights: E200K-PRNP mutation is the most common cause of fCJD. The typical presentation includes rapidly progressive dementia, myoclonus, cerebellar manifestations, and other motor signs. Early sensory disturbances and ...