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Creutzfeldt-jakob Dementia [demência Por Doença De Creutzfeldt-jakob]
(Colegio Brasileiro de Radiologia, 2015)
Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families
(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 ...
Evolución clínica y electroencefalográfica de un caso de probable enfermedad de Creutzfeldt-Jakob esporádica.Clinical and electrophysiological evolution of a case of sporadic Creutzfeldt-Jakob disease.
(Revista Mexicana de Neurociencia. Noviembre-Diciembre, 2012; Volumen 13: Numero 6. Rev Mex Neuroci 2012; 13 (6), 2015)
Forma familiar de la enfermedad de Creutzfeldt-Jakob: marcadores genéticos en 4 familias chilenas
(2006)
Background: Creutzfeldt-Jakob disease (CJD) is a form of
transmissible spongiform encephalopathy, in which a prion protein (PrPSc) accumulates in the
brain of affected individuals. Chile has a prevalence of CJD that is ...
Creutzfeldt-Jakob disease. Report of one case
(2016)
Creutzfeldt-Jakob disease has a higher incidence in Chile than in other countries. The post mortem pathological characterization of brain tissue is necessary to reach a definitive diagnosis. We report a 73 years old man ...
Enfermedad de creutzfeldt jakob: Hospital de San José, Bogotá D.C. Colombia
(Sociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la Salud, 2015-12-01)