When prion disease Isn’t suspected: prion disease as the cause of terminal decline in chronic mixed dementia-Reference-Cited by-同舟云学术

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When prion disease Isn’t suspected: prion disease as the cause of terminal decline in chronic mixed dementia

Published:2023-05-04 Issue:3 Volume:29 Page:92-97
ISSN:1355-4794
Container-title:Neurocase
language:en
Short-container-title:Neurocase

Author:

Krishnamurthy Sudarshan¹^ORCID,Harrison William²,Craft Suzanne¹,Lockhart Samuel N.¹,Bateman James R.³^ORCID

Affiliation:

1. Department of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA

2. Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC, USA

3. Department of Neurology, Wake Forest University School of Medicine, Winston-Salem, NC, USA

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/13554794.2024.2346990

Reference31 articles.

1. Diagnosis and Management of Dementia: Review

2. Unusual Clinical Presentations Challenging the Early Clinical Diagnosis of Creutzfeldt-Jakob Disease

3. Synergistic Interactions between A , Tau, and -Synuclein: Acceleration of Neuropathology and Cognitive Decline

4. Coexistence of mixed phenotype Creutzfeldt-Jakob disease, Lewy body disease and argyrophilic grain disease plus histological features of possible Alzheimer's disease: A multi-protein disorder in an autopsy case

5. Prevalence of dementia subtypes in United States Medicare fee‐for‐service beneficiaries, 2011–2013

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