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January 1, 1998Annals of Neurology

Detection of 14‐3‐3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt‐Jakob disease

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Authors

IZInga ZerrUniversitätsmedizin GöttingenMBMonika BodemerUniversity of GöttingenOGOlaf GefellerFriedrich-Alexander-Universität Erlangen-Nürnberg

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Zerr et al. (1998) studied this question.

synapsesocial.com/papers/6a869dfa3fdc309f7a6ed456https://doi.org/10.1002/ana.410430109
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Also Consider

Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Creutzfeldt‐Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering1979 · 629 citations
  2. 2Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene.1995 · 47 citations