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2. [A case of probable Creutzfeldt-Jakob disease with a point mutation of prion protein gene codon 180 and atypical MRI findings]. Kobayashi S; Ohuchi T; Maki T Rinsho Shinkeigaku; 1997 Aug; 37(8):671-4. PubMed ID: 9404141 [TBL] [Abstract][Full Text] [Related]
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8. Cerebral amyloid angiopathy with co-localization of prion protein and beta-amyloid in an 85-year-old patient with sporadic Creutzfeldt-Jakob disease. Paquet C; Privat N; Kaci R; Polivka M; Dupont O; Haïk S; Laplanche JL; Hauw JJ; Gray F Acta Neuropathol; 2008 Nov; 116(5):567-73. PubMed ID: 18551298 [TBL] [Abstract][Full Text] [Related]
9. Microsphere formation in a subtype of Creutzfeldt-Jakob disease with a V180I mutation and codon 129 MM polymorphism. Honda H; Ishii R; Hamano A; Itoh K; Suzuki SO; Fushiki S; Nakagawa M; Iwaki T Neuropathol Appl Neurobiol; 2013 Dec; 39(7):844-8. PubMed ID: 23531090 [No Abstract] [Full Text] [Related]
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