The factors that modulate the transmissibility of Transmissible Spongiform Encephalopathies
(TSE) and the approaches for the study of their zoonotic potential are reviewed. The paper …

Reports of neurological problems are increasing for the clinical presentation of coronavirus
disease-2019 (COVID-19). The clinical presentation reported in this study seemed to be a …

Sporadic Creutzfeldt–Jakob disease (CJD) is a major human prion disease worldwide. CJD
is a fatal neurodegenerative disease caused by an abnormal prion protein (PrPSc). To date …

Abstract Introduction: Creutzfeldt-Jakob disease (CJD) as a prion disease is an untreatable
type of progressive neurodegenerative encephalopathy. Although no definitive case has …

Abstract Sporadic Creutzfeldt-Jakob disease (CJD) is the most common prion disease,
resulting in rapid neurocognitive decline, and is universally lethal. CJD has a confounding …

Interventions: Supportive treatment. Outcomes: After 2 months of active treatment, the
patient's condition had not improved, and the patient died 82 days after admission. Lessons …

Creutzfeldt-Jakob disease (CJD) is a rare, rapidly progressive, and incurable
neurodegenerative disorder caused by prions. It is invariably fatal and classified under …

Designa-se por “príon” a forma alterada de uma proteína da superfície neuronal. Os príons
são notáveis pelo fato de serem capazes de induzirem sua contraparte normal a assumir a …

Creutzfeldt-Jakob disease is a rare, transmissible neurodegenerative disorder, most
prevalent between the ages of 50 and 70 years old, that is incurable and fatal. It's caused by …

Creutzfeldt-Jakob Disease and Organophosphorus: Is There a Relationship or Just a
Coincidence? Page 1 Array Publishers Page 1 of 3 Copyright © 2023 : Abdoulaye Mamadou …