Human Prion Diseases in The Netherlands (1998–2009): Clinical, Genetic and Molecular Aspects

Prion diseases are rare and fatal neurodegenerative disorders that can be sporadic, inherited or acquired by infection. Based on a national surveillance program in the Netherlands we describe here the clinical, neuropathological, genetic and molecular characteristics of 162 patients with neuropathol...

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Detalles Bibliográficos
Autores principales: Jansen, Casper, Parchi, Piero, Capellari, Sabina, Ibrahim-Verbaas, Carla A., Schuur, Maaike, Strammiello, Rosaria, Corrado, Patrizia, Bishop, Matthew T., van Gool, Willem A., Verbeek, Marcel M., Baas, Frank, van Saane, Wesley, Spliet, Wim G. M., Jansen, Gerard H., van Duijn, Cornelia M., Rozemuller, Annemieke J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340342/
https://www.ncbi.nlm.nih.gov/pubmed/22558438
http://dx.doi.org/10.1371/journal.pone.0036333

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