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Items: 1 to 20 of 22

1.

Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein.

Zou WQ, Puoti G, Xiao X, Yuan J, Qing L, Cali I, Shimoji M, Langeveld JP, Castellani R, Notari S, Crain B, Schmidt RE, Geschwind M, Dearmond SJ, Cairns NJ, Dickson D, Honig L, Torres JM, Mastrianni J, Capellari S, Giaccone G, Belay ED, Schonberger LB, Cohen M, Perry G, Kong Q, Parchi P, Tagliavini F, Gambetti P.

Ann Neurol. 2010 Aug;68(2):162-72. doi: 10.1002/ana.22094.

2.

Variably protease-sensitive prionopathy in the UK: a retrospective review 1991-2008.

Head MW, Yull HM, Ritchie DL, Langeveld JP, Fletcher NA, Knight RS, Ironside JW.

Brain. 2013 Apr;136(Pt 4):1102-15. doi: 10.1093/brain/aws366. Review. Erratum in: Brain. 2013 Nov;136(Pt 11):i1.

PMID:
23550113
3.

Prions in variably protease-sensitive prionopathy: an update.

Zou WQ, Gambetti P, Xiao X, Yuan J, Langeveld J, Pirisinu L.

Pathogens. 2013 Jul 5;2(3):457-71. doi: 10.3390/pathogens2030457. Review.

4.

The prion diseases: Creutzfeldt-Jakob, Gerstmann-Sträussler-Scheinker, and related disorders.

Mastrianni JA.

J Geriatr Psychiatry Neurol. 1998 Summer;11(2):78-97. Review.

PMID:
9877529
5.

An inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneity.

Yamada M, Itoh Y, Inaba A, Wada Y, Takashima M, Satoh S, Kamata T, Okeda R, Kayano T, Suematsu N, Kitamoto T, Otomo E, Matsushita M, Mizusawa H.

Neurology. 1999 Jul 13;53(1):181-8. Review.

PMID:
10408557
6.

An overview of human prion diseases.

Imran M, Mahmood S.

Virol J. 2011 Dec 24;8:559. doi: 10.1186/1743-422X-8-559. Review.

7.

Prion protein amyloidosis.

Ghetti B, Piccardo P, Frangione B, Bugiani O, Giaccone G, Young K, Prelli F, Farlow MR, Dlouhy SR, Tagliavini F.

Brain Pathol. 1996 Apr;6(2):127-45. Review.

PMID:
8737929
8.

Prion protein transgenes and the neuropathology in prion diseases.

DeArmond SJ, Prusiner SB.

Brain Pathol. 1995 Jan;5(1):77-89. Review.

PMID:
7767493
9.

Molecular pathogenesis of sporadic prion diseases in man.

Safar JG.

Prion. 2012 Apr-Jun;6(2):108-15. doi: 10.4161/pri.18666. Review.

10.

Molecular pathology of human prion diseases.

Kovacs GG, Budka H.

Int J Mol Sci. 2009 Mar;10(3):976-99. doi: 10.3390/ijms10030976. Review.

11.

Genetics of human prion disease.

Ridley RM, Baker HF.

Dev Biol Stand. 1993;80:15-23. Review.

PMID:
7903647
12.

The prion diseases.

Mastrianni JA, Roos RP.

Semin Neurol. 2000;20(3):337-52. Review.

PMID:
11051298
13.

Genetic and infectious prion diseases.

Prusiner SB.

Arch Neurol. 1993 Nov;50(11):1129-53. Review.

PMID:
8105771
14.

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.

Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E.

Brain Pathol. 1995 Jan;5(1):43-51. Review.

PMID:
7767490
15.

Human prion diseases: from Kuru to variant Creutzfeldt-Jakob disease.

Sikorska B, Liberski PP.

Subcell Biochem. 2012;65:457-96. doi: 10.1007/978-94-007-5416-4_17. Review.

PMID:
23225013
16.

[A trend of molecular genetics on prion diseases and prion protein].

Muramatsu Y, Shinagawa M.

Nihon Rinsho. 1993 Sep;51(9):2494-502. Review. Japanese.

PMID:
8411733
17.

Contribution of neuropathology to the understanding of human prion disease.

Kovács GG, Kalev O, Budka H.

Folia Neuropathol. 2004;42 Suppl A:69-76. Review.

PMID:
15449461
18.

Prions mediated neurodegenerative disorders.

Huang WJ, Chen WW, Zhang X.

Eur Rev Med Pharmacol Sci. 2015 Nov;19(21):4028-34. Review.

19.

Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis.

Capellari S, Strammiello R, Saverioni D, Kretzschmar H, Parchi P.

Acta Neuropathol. 2011 Jan;121(1):21-37. doi: 10.1007/s00401-010-0760-4. Review.

PMID:
20978903
20.

The role of PrP in health and disease.

Flechsig E, Weissmann C.

Curr Mol Med. 2004 Jun;4(4):337-53. Review.

PMID:
15354865
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