Results 181 to 190 of about 7,037 (201)
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FLAIR MRI in sporadic Creutzfeldt–Jakob disease

Neurology, 2000
Creutzfeldt–Jakob disease (CJD) is a rapidly progressive and ultimately lethal dementing illness caused by an infectious protein named prion. Besides cognitive decline and psychiatric or behavioral abnormalities, various other neurologic deficits appear. Myoclonic jerking, in particular startle myoclonus, is seen most commonly.
A F, Vrancken, C J, Frijns, L M, Ramos
openaire   +2 more sources

Variant or sporadic Creutzfeldt-Jakob disease?

The Lancet, 2010
1raises a major question for the future of variant Creutzfeldt-Jakob disease (vCJD) epidemics and suggests the occurrence of a second wave in the heterozygous population. In the reported case, diagnosis was based on clinical fi ndings and the results of magnetic resonance imaging (MRI).
J-P Brandel   +4 more
openaire   +1 more source

Atypical and early symptoms of sporadic Creutzfeldt – Jakob disease: case series and review of the literature

International Journal of Neuroscience, 2021
Ioannis E Dagklis, Dimitrios Ntantos
exaly  

Analysis of Chinese patients with sporadic Creutzfeldt-Jakob disease

Prion, 2020
Jiao Liu, Xueping Chen, Huifang Shang
exaly  

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