166 related articles for article (PubMed ID: 33586250)
1. Genetic Creutzfeldt-Jakob disease-M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case.
Shintaku M; Nakamura T; Kaneda D; Shinde A; Kusaka H; Takeuchi A; Kitamoto T
Neuropathology; 2021 Jun; 41(3):206-213. PubMed ID: 33586250
[TBL] [Abstract][Full Text] [Related]
2. V180I genetic Creutzfeldt-Jakob disease: Severe degeneration of the inferior olivary nucleus in an autopsied patient with identification of the M2T prion strain.
Watanabe M; Nakamura K; Saito R; Takeuchi A; Takahashi T; Kitamoto T; Onodera O; Kakita A
Neuropathology; 2023 Dec; 43(6):479-485. PubMed ID: 37165430
[TBL] [Abstract][Full Text] [Related]
3. Creutzfeldt-Jakob disease with an M232R substitution: report of a patient showing slowly progressive disease with abundant plaque-like PrP deposits in the cerebellum.
Shimizu H; Yamada M; Matsubara N; Takano H; Umeda Y; Kawase Y; Kitamoto T; Nishizawa M; Takahashi H
Neuropathology; 2009 Dec; 29(6):735-43. PubMed ID: 19422537
[TBL] [Abstract][Full Text] [Related]
4. An autopsied case of Creutzfeldt-Jakob disease with mutation in the prion protein gene codon 232 and type 1+2 prion protein.
Iwasaki Y; Yokoi F; Tatsumi S; Mimuro M; Iwai K; Kitamoto T; Yoshida M
Neuropathology; 2013 Oct; 33(5):568-75. PubMed ID: 23320809
[TBL] [Abstract][Full Text] [Related]
5. Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.
Baiardi S; Rossi M; Mammana A; Appleby BS; Barria MA; Calì I; Gambetti P; Gelpi E; Giese A; Ghetti B; Herms J; Ladogana A; Mikol J; Pal S; Ritchie DL; Ruf V; Windl O; Capellari S; Parchi P
Acta Neuropathol; 2021 Oct; 142(4):707-728. PubMed ID: 34324063
[TBL] [Abstract][Full Text] [Related]
6. MM2-thalamic-type sporadic Creutzfeldt-Jakob disease with widespread neocortical pathology.
Hirose K; Iwasaki Y; Izumi M; Yoshida M; Hashizume Y; Kitamoto T; Sahashi K
Acta Neuropathol; 2006 Oct; 112(4):503-11. PubMed ID: 16957926
[TBL] [Abstract][Full Text] [Related]
7. An autopsied case of MM1 + MM2-cortical with thalamic-type sporadic Creutzfeldt-Jakob disease presenting with hyperintensities on diffusion-weighted MRI before clinical onset.
Iwasaki Y; Mori K; Ito M; Mimuro M; Kitamoto T; Yoshida M
Neuropathology; 2017 Feb; 37(1):78-85. PubMed ID: 27436355
[TBL] [Abstract][Full Text] [Related]
8. An autopsy case of MM2-cortical + thalamic-type sporadic Creutzfeldt-Jakob disease.
Saito Y; Iwasaki Y; Aiba I; Kitamoto T; Yoshida M; Hashizume Y
Neuropathology; 2011 Oct; 31(5):523-30. PubMed ID: 21175861
[TBL] [Abstract][Full Text] [Related]
9. Creutzfeldt-Jakob disease with the M232R mutation in the prion protein gene in two cases showing different disease courses: a clinicopathological study.
Takeda N; Yokota O; Terada S; Haraguchi T; Nobukuni K; Mizuki R; Honda H; Yoshida H; Kishimoto Y; Oshima E; Ishizu H; Satoh K; Kitamoto T; Ihara Y; Uchitomi Y
J Neurol Sci; 2012 Jan; 312(1-2):108-16. PubMed ID: 21983261
[TBL] [Abstract][Full Text] [Related]
10. An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion protein.
Hama T; Iwasaki Y; Niwa H; Yoshida M; Hashizume Y; Kitamoto T; Murakami N; Sobue G
Neuropathology; 2009 Dec; 29(6):727-34. PubMed ID: 19422533
[TBL] [Abstract][Full Text] [Related]
11. A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.
Rodríguez-Martínez AB; Garrido JM; Zarranz JJ; Arteagoitia JM; de Pancorbo MM; Atarés B; Bilbao MJ; Ferrer I; Juste RA
BMC Neurol; 2010 Oct; 10():99. PubMed ID: 20973975
[TBL] [Abstract][Full Text] [Related]
12. MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology.
Hoshino A; Iwasaki Y; Izumi M; Kimura S; Ibi T; Kitamoto T; Yoshida M; Hashizume Y; Sahashi K
Neuropathology; 2008 Jun; 28(3):326-32. PubMed ID: 18248577
[TBL] [Abstract][Full Text] [Related]
13. Autopsy case of MV2K-type sporadic Creutzfeldt-Jakob disease with spongiform changes of the cerebral cortex.
Iwasaki Y; Hiraga K; Ito S; Ando T; Akagi A; Riku Y; Mimuro M; Miyahara H; Kobayashi A; Kitamoto T; Yoshida M
Neuropathology; 2019 Dec; 39(6):452-460. PubMed ID: 31515858
[TBL] [Abstract][Full Text] [Related]
14. Sporadic Creutzfeldt-Jakob disease VM1: phenotypic and molecular characterization of a novel subtype of human prion disease.
Gelpi E; Baiardi S; Nos C; Dellavalle S; Aldecoa I; Ruiz-Garcia R; Ispierto L; Escudero D; Casado V; Barranco E; Boltes A; Molina-Porcel L; Bargalló N; Rossi M; Mammana A; Tiple D; Vaianella L; Stoegmann E; Simonitsch-Klupp I; Kasprian G; Klotz S; Höftberger R; Budka H; Kovacs GG; Ferrer I; Capellari S; Sanchez-Valle R; Parchi P
Acta Neuropathol Commun; 2022 Aug; 10(1):114. PubMed ID: 35978418
[TBL] [Abstract][Full Text] [Related]
15. Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures.
Cassard H; Huor A; Espinosa JC; Douet JY; Lugan S; Aron N; Vilette D; Delisle MB; Marín-Moreno A; Peran P; Beringue V; Torres JM; Ironside JW; Andreoletti O
mBio; 2020 Jun; 11(3):. PubMed ID: 32546613
[TBL] [Abstract][Full Text] [Related]
16. Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease.
Ironside JW; Head MW
Curr Top Microbiol Immunol; 2004; 284():133-59. PubMed ID: 15148991
[TBL] [Abstract][Full Text] [Related]
17. Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone.
Cali I; Miller CJ; Parisi JE; Geschwind MD; Gambetti P; Schonberger LB
Acta Neuropathol Commun; 2015 Jun; 3():37. PubMed ID: 26108478
[TBL] [Abstract][Full Text] [Related]
18. Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British woman.
Mead S; Joiner S; Desbruslais M; Beck JA; O'Donoghue M; Lantos P; Wadsworth JD; Collinge J
Arch Neurol; 2007 Dec; 64(12):1780-4. PubMed ID: 18071044
[TBL] [Abstract][Full Text] [Related]
19. Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein Gene.
Marcon G; Indaco A; Di Fede G; Suardi S; Finato N; Moretti V; Micoli S; Fociani P; Zerbi P; Pincherle A; Redaelli V; Tagliavini F; Giaccone G
Brain Pathol; 2014 Mar; 24(2):148-51. PubMed ID: 24118545
[TBL] [Abstract][Full Text] [Related]
20. MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and PrPSc type 2 in Japan.
Fukushima R; Shiga Y; Nakamura M; Fujimori J; Kitamoto T; Yoshida Y
J Neurol Neurosurg Psychiatry; 2004 Mar; 75(3):485-7. PubMed ID: 14966171
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
