Prion propagation and cellular dysfunction in prion disease: Disconnecting the dots
ST Foliaki, CL Haigh - PLoS Pathogens, 2023 - journals.plos.org
AU: Pleaseconfirmthatallheadinglevelsarerepre…. Prion diseases are rare and incurable
neurodegenerative diseases caused by misfolding of prion protein (PrP) into abnormal …
neurodegenerative diseases caused by misfolding of prion protein (PrP) into abnormal …
Unmet needs of biochemical biomarkers for human prion diseases
Although the development of aggregation assays has noticeably improved the accuracy of
the clinical diagnosis of prion diseases, research on biomarkers remains vital. The major …
the clinical diagnosis of prion diseases, research on biomarkers remains vital. The major …
Association of glymphatic function with clinical characteristics in patients with clinical and asymptomatic Creutzfeldt-Jakob disease
Z Chen, D Jiang, Y Kong, J Zhang, C Min, S Bi, S Yan… - Neurology, 2025 - neurology.org
Background and Objectives Abnormal glymphatic system–related proteins have been
identified in a small-scale pathologic study of patients with Creutzfeldt-Jakob disease (CJD) …
identified in a small-scale pathologic study of patients with Creutzfeldt-Jakob disease (CJD) …
Metabolic Brain Changes Can Predict the Underlying Pathology in Neurodegenerative Brain Disorders: A Case Report of Sporadic Creutzfeldt–Jakob Disease with …
T Rus, J Mlakar, J Jamšek, M Trošt - International Journal of Molecular …, 2023 - mdpi.com
The co-occurrence of multiple proteinopathies is being increasingly recognized in
neurodegenerative disorders and poses a challenge in differential diagnosis and patient …
neurodegenerative disorders and poses a challenge in differential diagnosis and patient …
[HTML][HTML] Reconfigured metabolism brain network in asymptomatic Creutzfeldt-Jakob disease
Y Kong, Z Chen, J Zhang, Y Wang, M Chu, H Nan… - Neurobiology of …, 2025 - Elsevier
Background Investigating brain metabolic networks is crucial for understanding the
pathogenesis and functional alterations in Creutzfeldt-Jakob disease (CJD). However …
pathogenesis and functional alterations in Creutzfeldt-Jakob disease (CJD). However …
[HTML][HTML] Characteristics of Creutzfeldt-Jakob disease at Siriraj Hospital, Thailand: Case series and literature review
C Dumrikarnlert, N Kanokkawinwong… - Clinical Parkinsonism & …, 2024 - Elsevier
Abstract Introduction Creutzfeldt-Jakob disease (CJD) is a rare, rapidly progressive, fatal,
neurodegenerative disease classified as prion diseases. There are many subtypes of this …
neurodegenerative disease classified as prion diseases. There are many subtypes of this …
[PDF][PDF] Clinical Parkinsonism & Related Disorders
C Dumrikarnlert, N Kanokkawinwong… - researchgate.net
ABSTRACT Introduction: Creutzfeldt-Jakob disease (CJD) is a rare, rapidly progressive,
fatal, neurodegenerative disease classified as prion diseases. There are many subtypes of …
fatal, neurodegenerative disease classified as prion diseases. There are many subtypes of …
[PDF][PDF] Metabolic brain imaging and network analysis in neurodegenerative dementias
M Perovnik - neurocare.si
Conclusions: The new disease-modifying drugs for neurodegenerative dementias (40, 41)
will undoubtably change the field and precise imaging biomarkers are necessary for correct …
will undoubtably change the field and precise imaging biomarkers are necessary for correct …
[引用][C] Bovine Spongiform Encephalopathy," Mad Cow's Disease" and Variant Creutzfeldt-Jakob Disease in Humans: A Critical Update.
Bovine Spongiform Encephalopathy, "Mad Cow's Disease" and Variant Creutzfeldt-Jakob
Disease in Humans: A Critical Update. - Abstract - Europe PMC Sign in | Create an account …
Disease in Humans: A Critical Update. - Abstract - Europe PMC Sign in | Create an account …