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Canadian Creutzfeldt-Jakob disease incidence remained stable during the coronavirus disease (COVID-19) pandemic. [PDF]
Front NeurolSlota JA +11 more
europepmc +1 more source
Estimating future variant Creutzfeldt-Jakob disease cases in the UK: a cohort-based probabilistic model. [PDF]
Lancet Reg Health EurRoberts B +8 more
europepmc +1 more source
From early symptoms to EEG silence: tracking the neurodegenerative course of sporadic Creutzfeldt-Jakob disease. [PDF]
Front Hum NeurosciHe Y, Qiu L.
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Correction: <i>Variant Creutzfeldt-Jakob disease in UK children after 27 years of active prospective surveillance</i>. [PDF]
Arch Dis Childeuropepmc +1 more source
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Variant Creutzfeldt-Jakob disease
The Lancet, 1999It is clear that the prion strain causing bovine spongiform encephalopathy (BSE) in cattle has infected human beings, manifesting itself as a novel human prion disease, variant Creutzfeldt-Jakob disease (CjD). Studies of the incubation periods seen in previous epidemics of human prion disease and of the effect of transmission barriers limiting spread ...
John Collinge
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Neurologic Clinics, 1986
There has been significant advance in our understanding of CJD and similar spongiform encephalopathies in recent years. The range in clinical expression of the disease is better appreciated, and the existence of "atypical" cases of CJD is increasingly recognized.
Z, Davanipour, M, Alter, E, Sobel
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There has been significant advance in our understanding of CJD and similar spongiform encephalopathies in recent years. The range in clinical expression of the disease is better appreciated, and the existence of "atypical" cases of CJD is increasingly recognized.
Z, Davanipour, M, Alter, E, Sobel
openaire +2 more sources
Archives of Neurology, 1971
IN 1920, Hans Gerhard Creutzfeldt of Berlin (1885 to 1964) published a detailed case report of a patient with an unusual combination of neurological signs and pathological findings.1,2Then within three years, the neuropathologist Alfons Jakob of Hamburg (1884 to 1931), a student of Nissl and Alzheimer,3described five similar cases and established this ...
R H, Wilkins, I A, Brody
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IN 1920, Hans Gerhard Creutzfeldt of Berlin (1885 to 1964) published a detailed case report of a patient with an unusual combination of neurological signs and pathological findings.1,2Then within three years, the neuropathologist Alfons Jakob of Hamburg (1884 to 1931), a student of Nissl and Alzheimer,3described five similar cases and established this ...
R H, Wilkins, I A, Brody
openaire +2 more sources
Neuropathology, 2000
It is valuable to summarize the milestone study of prion diseases done in Japan for review in the journal Neuropathology in 2000. Many studies done in Japan promote world prion research activity, and also influence further research projects in other groups abroad.
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It is valuable to summarize the milestone study of prion diseases done in Japan for review in the journal Neuropathology in 2000. Many studies done in Japan promote world prion research activity, and also influence further research projects in other groups abroad.
openaire +4 more sources