177 related articles for article (PubMed ID: 19130739)
1. A patient with MV2 subtype of sporadic Creutzfeldt-Jakob disease and atypical clinical presentation.
Guerrero D; Martínez-Velilla N; Caballero MC; Mendióroz MT; Tuñón T; Masdeu J; Rodríguez A; Armstrong J; Ferrer I
Clin Neuropathol; 2008; 27(6):408-13. PubMed ID: 19130739
[TBL] [Abstract][Full Text] [Related]
2. Extensive cortical spongiform changes with cerebellar small amyloid plaques: the clinicopathological case of MV2K+C subtype in Creutzfeldt-Jakob disease.
Araki K; Nakano Y; Kobayashi A; Matsudaira T; Sugiura A; Takao M; Kitamoto T; Murayama S; Obi T
Neuropathology; 2014 Dec; 34(6):541-6. PubMed ID: 24984899
[TBL] [Abstract][Full Text] [Related]
3. An autopsied case of MV2K + C-type sporadic Creutzfeldt-Jakob disease presenting with widespread cerebral cortical involvement and Kuru plaques.
Iwasaki Y; Saito Y; Aiba I; Kobayashi A; Mimuro M; Kitamoto T; Yoshida M
Neuropathology; 2017 Jun; 37(3):241-248. PubMed ID: 28568896
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.
Faucheux BA; Morain E; Diouron V; Brandel JP; Salomon D; Sazdovitch V; Privat N; Laplanche JL; Hauw JJ; Haïk S
Neuropathol Appl Neurobiol; 2011 Aug; 37(5):500-12. PubMed ID: 21450052
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Defining the phenotypic spectrum of sporadic Creutzfeldt-Jakob disease MV2K: the kuru plaque type.
Baiardi S; Mammana A; Dellavalle S; Rossi M; Redaelli V; Colaizzo E; Di Fede G; Ladogana A; Capellari S; Parchi P
Brain; 2023 Aug; 146(8):3289-3300. PubMed ID: 36883639
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.
Kobayashi A; Parchi P; Yamada M; Mohri S; Kitamoto T
Neuropathology; 2016 Jun; 36(3):305-10. PubMed ID: 26669818
[TBL] [Abstract][Full Text] [Related]
11. An autopsy case of MV 2K + C subtype of Creutzfeldt-Jakob disease.
Uchino A; Saito Y; Tokuda S; Saburo Y; Murayama S; Hasegawa K
Neuropathology; 2024 Feb; ():. PubMed ID: 38353038
[TBL] [Abstract][Full Text] [Related]
12. An autopsy case of MV2K-type sporadic Creutzfeldt-Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings.
Matsuo K; Goto D; Hasegawa M; Ogita K; Koyama T; Akagi A; Kitamoto T; Yoshida M; Iwasaki Y
Neuropathology; 2022 Jun; 42(3):245-253. PubMed ID: 35441383
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
Schmitz M; Lüllmann K; Zafar S; Ebert E; Wohlhage M; Oikonomou P; Schlomm M; Mitrova E; Beekes M; Zerr I
Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565
[TBL] [Abstract][Full Text] [Related]
16. Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature.
Rossi M; Saverioni D; Di Bari M; Baiardi S; Lemstra AW; Pirisinu L; Capellari S; Rozemuller A; Nonno R; Parchi P
Acta Neuropathol Commun; 2017 Nov; 5(1):87. PubMed ID: 29169405
[TBL] [Abstract][Full Text] [Related]
17. A case of MV2K subtype of sporadic Creutzfeldt-Jakob disease with florid-like plaques: Similarities and differences to variant Creutzfeldt-Jakob disease.
Bošnjak M; Zupan A; Fiorini M; Popović KŠ; Popović M
Neuropathology; 2020 Aug; 40(4):389-398. PubMed ID: 32249464
[TBL] [Abstract][Full Text] [Related]
18. Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.
Galeno R; Di Bari MA; Nonno R; Cardone F; Sbriccoli M; Graziano S; Ingrosso L; Fiorini M; Valanzano A; Pasini G; Poleggi A; Vinci R; Ladogana A; Puopolo M; Monaco S; Agrimi U; Zanusso G; Pocchiari M
J Virol; 2017 Jun; 91(11):. PubMed ID: 28298604
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease.
Schulz-Schaeffer WJ; Giese A; Windl O; Kretzschmar HA
Clin Neuropathol; 1996; 15(6):353-7. PubMed ID: 8937783
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
