Results 211 to 220 of about 13,613 (255)

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

Experimental Neurology, 1989
A host protein encoded by the gene specifying the scrapie amyloid precursor affects pathogenesis of the transmissible spongiform encephalopathies: Creutzfeldt-Jakob disease (CJD), Gerstmann-Sträussler-Scheinker's syndrome (GSS), and kuru in man, and scrapie in animals.
D, Goldgaber, L G, Goldfarb, P, Brown, D M, Asher, W T, Brown, S, Lin, J W, Teener, S M, Feinstone, R, Rubenstein, R J, Kascsak   +9 more
openaire   +2 more sources

[A note on the epidemiology of Creutzfeldt-Jakob syndrome].

Revue neurologique, 1998
The annual incidence of sporadic Jakob-Creuzfeldt disease has been stable for the last 30 years. The new variant affecting young adults which appeared in the United Kingdom (20 cases) and France (1 case) in 1994 is due to the same infectious agent which causes bovine spongiform encephalopathy.
A, Alpérovitch, N, Delasnerie-Lauprêtre, J P, Brandel   +2 more
openaire   +1 more source

Creutzfeldt-Jakob disease presenting with Capgras syndrome

2023
Narinder Kapur, Norman Poole
openaire   +1 more source

[Creutzfeldt-Jakob disease(CJD) and Gerstmann-Sträussler-Scheinker syndrome(GSS)].

Nihon rinsho. Japanese journal of clinical medicine, 1997
Prion diseases are now a focus of attention since the diseases are known to disseminate beyond expectation. They are various types of Gerstmann-Sträussler-Scheinker syndrome(GSS), fatal familial insomnia, iatrogenic Creutzfeldt-Jakob disease(CJD), and variant CJD which suspected to have disseminated from bovine spongiform encephalopathy. Abnormal prion
F, Udaka, M, Fujisawa, M, Kameyama
openaire   +1 more source

Encéphalopathie spongieuse de la présénilité et syndrome de Creutzfeldt-Jakob

1967
Les 7 cas de maladie de Creutzfeldt-Jakob, ont une provenance diverse: quatre d’entre eux font partie du materiel du Professeur Garcin, trois autres, sont encore inedits.
openaire   +1 more source

[Creutzfeldt-Jakob syndromes].

La Nouvelle presse medicale, 1972
J J, Hauw, J L, Ribadeau-Dumas
openaire   +1 more source

The Creutzfeldt-Jakob syndrome.

Bulletin of the Los Angeles Neurological Society, 1998
L H, WARICK, H S, BAROWS
openaire   +1 more source

Sporadische Creutzfeldt-Jakob-Erkrankung imitiert posteriores reversibles Enzephalopathie-Syndrom

Der Nervenarzt, 2019
Schulamith Krüger, Jörg Larsen, Jens Schaumberg   +2 more
openaire   +1 more source

The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob disease

Lancet, The, 2000
James W Ironside
exaly  

[Creutzfeldt-Jakob. Disease or syndrome].

Annales medico-psychologiques, 1980
J, Nehlil, J C, Loutre, R, Renouardiere, P, Fleury   +3 more
openaire   +1 more source