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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Public Library of Science 2012
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3340342/
https://ncbi.nlm.nih.gov/pubmed/22558438
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0036333
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