Results 181 to 190 of about 7,037 (201)
Some of the next articles are maybe not open access.
FLAIR MRI in sporadic Creutzfeldt–Jakob disease
Neurology, 2000Creutzfeldt–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, 20101raises 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
Surgery and Risk of Sporadic Creutzfeldt-Jakob Disease
Neuroepidemiology, 2008Hester J T, Ward, Richard S G, Knight
openaire +2 more sources
Analysis of Chinese patients with sporadic Creutzfeldt-Jakob disease
Prion, 2020Jiao Liu, Xueping Chen, Huifang Shang
exaly
Surgical treatment and risk of sporadic Creutzfeldt-Jakob disease: a case-control study
Lancet, The, 1999Matthew Law, Alison Boyd
exaly

