Results 121 to 130 of about 7,669 (173)

Rapidly progressive dementia in a middle-aged woman: A case of probable sporadic Creutzfeldt-Jakob disease. [PDF]

open access: yesMed Int (Lond)
Jarquín-Rios VR   +4 more
europepmc   +1 more source

The Phenotypic Spectrum of Sporadic Creutzfeldt-Jakob Disease Cortical Subtype. [PDF]

open access: yesAnn Neurol
Baiardi S   +16 more
europepmc   +1 more source

First Case of Creutzfeldt-Jakob Disease in Ghana: Diagnostic Challenge in a Resource-Limited Setting. [PDF]

open access: yesCase Rep Neurol
Obese V   +9 more
europepmc   +1 more source

[Creutzfeldt-Jakob syndrome. A new variant in Great Britain].

open access: yesTidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1996
openaire   +1 more source

Lithium-Induced Creutzfeldt-Jakob Syndrome

Clinical Neuropharmacology, 1996
a 67-year-old man with bipolar disorder developed a Creutzfeldt-Jakob like syndrome during lithium carbonate treatment. Lithium serum level was within the therapeutic range. Complete clinical-electroencephalographic recovery was achieved after lithium therapy was discontinued.
B, Casanova   +5 more
openaire   +2 more sources

Electroencephalographic and clinicopathological studies on Creutzfeldt-Jakob syndrome [PDF]

open access: yesJournal of Neurology, Neurosurgery and Psychiatry, 1976
The correlation between the appearance of the characteristic electroencephalographic abnormality, cardinal clinical manifestations, and neuropathological features was studied in four cases of Creutzfeldt-Jakob syndrome consisting of subacute spongiform encephalopathy and classical Creutzfeldt-Jakob disease.
K, Goto, H, Umezaki, M, Suetsugu
exaly   +3 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

Creutzfeldt-Jakob–Like Syndrome due to Hypercalcemic Encephalopathy

Clinical EEG and Neuroscience, 2014
Hypercalcemia can cause a subacute syndrome of progressive dementia and marked changes in the electroencephalogram (EEG). We report a case of iatrogenic hypercalcemia with a close correlation between the clinical course and the EEG changes. A 73-year-old woman presented with a subacute syndrome of progressive dementia and bursts of 1.5 to 2 Hz ...
Johannes, Rösche   +3 more
openaire   +2 more sources

Creutzfeldt-Jakob syndrome presenting as epilepsia partialis continua

Journal of Clinical Neuroscience, 2001
Creutzfeldt-Jakob disease (CJD) is an uncommon rapidly progressive neurological disorder which can have protean clinical presentations. We report an autopsy-proven case of CJD presenting initially as epilepsia partialis continua but then developing the typical clinical features of CJD over several weeks.
J, Parry   +3 more
openaire   +2 more sources

MRI Detection of the Cerebellar Syndrome in Creutzfeldt–Jakob Disease

The Cerebellum, 2009
Creutzfeldt-Jakob Disease (CJD) is characterized by bilateral basal ganglia hyperintensities on T2W and diffusion-weighted imaging (DWI) magnetic resonance imaging (MRI) scans, consistent with its extrapyramidal neurological manifestations. MRI is diagnostically uninformative about the cerebellar symptoms, equally prominent in CJD.
Oren S, Cohen   +5 more
openaire   +2 more sources

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