Evolution of Clinical, Electroencephalographic, and Radiological Changes in Sporadic Creutzfeldt-Jakob Disease
Creutzfeldt-Jakob disease (CJD) is a rare, progressive, and fatal disease. Sporadic CJD (sCJD) accounts for 85% of the CJD cases. It is characterized by rapidly progressive dementia, myoclonic jerks, and pyramidal, extrapyramidal, visual, and psychiatric symptoms. Electroencephalography (EEG) and ma...
Saved in:
Main Authors: | S. Sheetal (Author), Nikhil Gladson (Author), Joseph George (Author), T. Sithara (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2024-07-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Sporadic Creutzfeldt-Jakob disease with focal findings: caveats to current diagnostic criteria
by: Edward C. Mader, et al.
Published: (2013) -
A Systematic Review of Sporadic Creutzfeldt-Jakob Disease: Pathogenesis, Diagnosis, and Therapeutic Attempts
by: Maria Carolina Jurcau, et al.
Published: (2024) -
A polymorphism in the regulatory region of <it>PRNP </it>is associated with increased risk of sporadic Creutzfeldt-Jakob disease
by: Will Robert G, et al.
Published: (2011) -
Case Report of Clinically Probable Sporadic Creutzfeldt - Jakob Disease from A Tertiary Care Hospital in South India
by: Shaik Afsar Pasha, et al.
Published: (2017) -
A rare case of Sporadic Creutzfeldt-Jakob disease at a remote mountain hospital in the Indian Himalayan Region
by: Nitu Sharma, et al.
Published: (2024)