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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
Assuntos:
Research Article
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados