Results 151 to 160 of about 21,599 (190)
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Heidenhain Variant of Creutzfeldt-Jakob Disease with Concurrent Findings of Posterior Reversible Encephalopathy Syndrome: A Case Report and Literature Review

Neurographics, 2021
Although Creutzfeldt-Jakob disease is not yet proved to be related to the development of posterior reversible encephalopathy syndrome, prion invasion to the endothelium has been shown to change blood-brain barrier permeability.
Bruno Policeni
exaly   +2 more sources

Balint syndrome due to Creutzfeldt–Jakob disease

Neurology, 2004
Since Balint originally described a patient with striking disturbances in vision and movement,1 this syndrome has been reported to result from stroke, metastatic lesions, demyelinating disorders, carbon monoxide poisoning, corticobasal ganglionic degeneration, Alzheimer disease, and HIV infection.2 We report a patient with Balint syndrome resulting ...
B M, Ances   +6 more
openaire   +2 more sources

Diagnostic Utility of Cerebrospinal Fluid α-Synuclein in Creutzfeldt-Jakob Disease: A Systematic Review and Meta-Analysis

Journal of Alzheimer's Disease, 2022
Background: Creutzfeldt-Jakob disease (CJD) can be difficult to distinguish clinically from some non-prion neurological diseases. Previous studies have reported markedly increased levels of α-synuclein in cerebrospinal fluid (CSF) of CJD patients ...
Yu Kong   +4 more
semanticscholar   +1 more source

Dual-Phase 18F-FP-CIT PET in 2 Different Clinical Phenotypes of Sporadic Creutzfeldt-Jakob Disease.

Clinical Nuclear Medicine, 2022
Early diagnosis of Creutzfeldt-Jakob disease (CJD) patients is often challenging due to the low sensitivity of the current clinical diagnostic criteria.
K. Lee   +4 more
semanticscholar   +1 more source

Concurrent Duloxetine Withdrawal and Neuroleptic Malignant Syndrome Mimicking Creutzfeldt-Jakob Disease: A Case Report (P2.219)

Neurology, 2017
Objective: To describe a case of iatrogenically induced CJD symptoms. Background: The constellation of rapidly progressive dementia, myoclonus, rigidity, and hallucinations suggests a diagnosis of Creutzfeldt-Jakob Disease (CJD), particularly the ...
E. Zucker   +4 more
semanticscholar   +1 more source

Balint's syndrome revealing Creutzfeldt-Jakob disease

Revue Neurologique, 2022
M, Escalere   +5 more
openaire   +2 more sources

MV2 subtype of sporadic Creutzfeldt‐Jakob disease presenting as corticobasal syndrome

Movement Disorders, 2007
Clinicopathologic correlative studies have shown that the corticobasal syndrome (CBS) is associated with various pathologies, including PSP, AD or sporadic Creutzfeldt-Jakob disease (sCJD), in addition to corticobasal degeneration (CBD. sCJD is generally distinguished from CBD by the much shorter duration of illness and the finding of either a 14-3-3 ...
Anna Magherini   +5 more
openaire   +1 more source

[Case of Creutzfeldt-Jakob syndrome with involvement of the neostriatum].

Neurologia i neurochirurgia polska, 1983
The authors describe a case of CJD in a man aged 45 years. The disease began with sluggishness of movements and speech difficulties, followed by development of pyramidal system damage and dementia. EEG findings were normal throughout the whole duration of the disease that is 3.5 years. Neuropathological examination disclosed major neuronal loss, spongy
J, Kulczycki   +2 more
openaire   +1 more source

Drug‐induced creutzfeldt‐jakob like syndrome: A review

Human Psychopharmacology: Clinical and Experimental, 1992
AbstractCreutzfeldt‐Jakob disease is an untreatable degenerative disorder which presents problems in diagnosis. The clinical picture is said to be characterised by dementia, myoclonus and periodic triphasic discharge on the electroencephalogram. The high profile given to this disorder recently will lead inevitably to more diagnoses being made.
openaire   +1 more source

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