CareLit · DOI-Nachweis · Aktuelle Neurologie
Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 type
DOI 10.1055/s-2005-919530
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Nachweis in CareLit
Autor:innenB Meißner, K Kallenberg, I.M Westner, M Bartl, A Krasnianski, D Varges, H Kretzschmar, W.J Schulz-Schaeffer, I Zerr
ZeitschriftAktuelle Neurologie
Ausgabe10/2005
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Background: Creutzfeldt-Jakob disease (CJD) is a rare and fatal disease caused by prions. Recently, 6 molecular subtypes of sporadic CJD (sCJD) have been identified showing differences regarding the disease course, neuropathological lesion patterns and sensitivity to diagnostic tools. In the literature, only isolated cases of the rare VV1 subtype have been reported so far. We describe the clinical characteristics an…
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Zitierempfehlung
B Meißner, K Kallenberg, I.M Westner, M Bartl, A Krasnianski, D Varges, H Kretzschmar, W.J Schulz-Schaeffer, I Zerr (2005) Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 type. Aktuelle Neurologie (10). https://doi.org/10.1055/s-2005-919530
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