Clinicopathologic characteristics of sporadic Japanese Creutzfeldt–Jakob disease classified according to prion protein gene polymorphism and prion protein type

By Iwasaki Yasushi   Yoshida Mari   Hashizume Yoshio   Kitamoto Tetsuyuki   Sobue Gen  

Acta Neuropathologica, Vol. 112, Iss. 5, 2006-11 ,pp. : 561-571

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Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion

By Dermaut Bart   Cruts Marc   Backhovens Hubert   Lübcke Ursula   Van Everbroeck Bart   Sciot Raf   Dom René   Martin Jean-Jacques   Van Broeckhoven Christine   Cras Patrick  

Journal of Neurology, Vol. 247, Iss. 5, 2000-05 ,pp. : 364-368

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Erratum to: R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease

By Vita Maria   Gaudino Simona   Giuda Daniela   Sauchelli Donato   Alboini Paolo   Gangemi Emma   Bizzarro Alessandra   Scaricamazza Eugenia   Capellari Sabina   Parchi Piero   Masullo Carlo  

Journal of Neurology, Vol. 260, Iss. 12, 2013-12 ,pp. : 3199-3199

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Size frequency distributions of the florid prion protein aggregates in variant Creutzfeldt-Jakob disease follow a power-law function

By Armstrong R.   Cairns N.   Ironside J.  

Neurological Sciences, Vol. 27, Iss. 2, 2006-06 ,pp. : 104-109

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MM2-thalamic-type sporadic Creutzfeldt-Jakob disease with widespread neocortical pathology

By Hirose Kazunori   Iwasaki Yasushi   Izumi Masayuki   Yoshida Mari   Hashizume Yoshio   Kitamoto Tetsuyuki   Sahashi Ko  

Acta Neuropathologica, Vol. 112, Iss. 4, 2006-10 ,pp. : 503-511

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