MA Tranulis, SL Benestad, T Baron… - Topics in current …, 2011 - ncbi.nlm.nih.gov ... vCJD). Person-to-person spread of human prion disease has only been known to occur following cannibalism (kurudisease in Papua New Guinea) or through medical or surgical treatment (iatrogenic CJD, iCJD). In contrast ...
K Murray, J Peters, L Stellitano… - Journal of Neurology, …, 2011 - jnnp.bmj.com ... Prion. Transmissible spongiform encephalopathies (TSEs) are a group of neurodegenerative diseases including scrapie, bovine spongiform encephalopathy (BSE) and the human forms, Creutzfeldt–Jakob disease (CJD) and kuru. ... Cited by 3 - Related articles - All 3 versions
S Casper - Journal of the History of the Neurosciences, 2011 - Taylor & Francis Over the last three decades, neurological diseases and disorders have influenced public, intellectual, artistic, and political imaginations in important ways. Accordingly, much scholarship has sought to place such famous nervous conditions as epilepsy, hysteria, depression, ... Related articles - All 3 versions
[HTML] from nih.govJDF Wadsworth… - Acta neuropathologica, 2011 - Springer ... variant' CJD. Nature 383:685–690 35. Collinge J, Whitfield J, McKintosh E et al (2006) Kuru in the 21st century—an acquired human prion disease with very long incubation periods. Lancet 367:2068–2074 36. Collinge J, Whitfield ... Cited by 2 - Related articles - All 5 versions
[PDF] from fudan.edu.cnLV Sun - Journal of Molecular Cell Biology, 2011 - jmcb.oxfordjournals.org ... the population over 60 years old, up to 50% in that over 80 years old. Misfolded characteristic proteins are commonly seen in most neurodegenerative diseases, including both Lou Gehrigs's disease and CJD/Kurudisease. ... Related articles - All 5 versions
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