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Items: 1 to 20 of 136

1.

Sporadic Creutzfeldt-Jakob disease with unusual initial presentation as posterior reversible encephalopathy syndrome: a case report.

Dirzius E, Balnyte R, Steibliene V, Gleizniene R, Gudinaviciene I, Radziunas A, Petrikonis K.

BMC Neurol. 2016 Nov 22;16(1):234.

2.

Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice.

Jaumain E, Quadrio I, Herzog L, Reine F, Rezaei H, Andréoletti O, Laude H, Perret-Liaudet A, Haïk S, Béringue V.

J Virol. 2016 Nov 14;90(23):10867-10874.

PMID:
27681129
3.

Etiologic Framework for the Study of Neurodegenerative Disorders as Well as Vascular and Metabolic Comorbidities on the Grounds of Shared Epidemiologic and Biologic Features.

de Pedro-Cuesta J, Martínez-Martín P, Rábano A, Ruiz-Tovar M, Alcalde-Cabero E, Calero M.

Front Aging Neurosci. 2016 Jun 13;8:138. doi: 10.3389/fnagi.2016.00138.

4.

Prions: Beyond a Single Protein.

Das AS, Zou WQ.

Clin Microbiol Rev. 2016 Jul;29(3):633-58. doi: 10.1128/CMR.00046-15. Review.

PMID:
27226089
5.

A direct assessment of human prion adhered to steel wire using real-time quaking-induced conversion.

Mori T, Atarashi R, Furukawa K, Takatsuki H, Satoh K, Sano K, Nakagaki T, Ishibashi D, Ichimiya K, Hamada M, Nakayama T, Nishida N.

Sci Rep. 2016 Apr 26;6:24993. doi: 10.1038/srep24993.

6.
7.

The amyloid hypothesis of Alzheimer's disease at 25 years.

Selkoe DJ, Hardy J.

EMBO Mol Med. 2016 Jun 1;8(6):595-608. doi: 10.15252/emmm.201606210. Review.

8.

A case of Creutzfeldt-Jakob disease in a patient on hemodialysis.

Suh SH, Choi YH, Kim CS, Choi JS, Park JW, Bae EH, Ma SK, Kim BC, Kim SW.

Kidney Res Clin Pract. 2012 Mar;31(1):76-8. doi: 10.1016/j.krcp.2011.12.004.

9.

Emergence of two prion subtypes in ovine PrP transgenic mice infected with human MM2-cortical Creutzfeldt-Jakob disease prions.

Chapuis J, Moudjou M, Reine F, Herzog L, Jaumain E, Chapuis C, Quadrio I, Boulliat J, Perret-Liaudet A, Dron M, Laude H, Rezaei H, Béringue V.

Acta Neuropathol Commun. 2016 Feb 5;4:10. doi: 10.1186/s40478-016-0284-9.

10.

Gerstmann-Sträussler-Scheinker disease subtypes efficiently transmit in bank voles as genuine prion diseases.

Pirisinu L, Di Bari MA, D'Agostino C, Marcon S, Riccardi G, Poleggi A, Cohen ML, Appleby BS, Gambetti P, Ghetti B, Agrimi U, Nonno R.

Sci Rep. 2016 Feb 4;6:20443. doi: 10.1038/srep20443.

11.

Unusual presentations in patients with E200K familial Creutzfeldt-Jakob disease.

Cohen OS, Kimiagar I, Korczyn AD, Nitsan Z, Appel S, Hoffmann C, Rosenmann H, Kahana E, Chapman J.

Eur J Neurol. 2016 May;23(5):871-7. doi: 10.1111/ene.12955.

PMID:
26806765
12.

Insights into Mechanisms of Chronic Neurodegeneration.

Diack AB, Alibhai JD, Barron R, Bradford B, Piccardo P, Manson JC.

Int J Mol Sci. 2016 Jan 12;17(1). pii: E82. doi: 10.3390/ijms17010082. Review.

13.

Creutzfeldt-Jakob Disease in a Tertiary Care Hospital in Thailand: A Case Series and Review of the Literature.

Lolekha P, Rasheed A, Yotsarawat C.

J Mov Disord. 2015 Sep;8(3):136-40. doi: 10.14802/jmd.15014.

14.

Endemic Viruses of Squirrel Monkeys (Saimiri spp.).

Rogers DL, McClure GB, Ruiz JC, Abee CR, Vanchiere JA.

Comp Med. 2015 Jun;65(3):232-40. Review.

15.

Transmission of scrapie prions to primate after an extended silent incubation period.

Comoy EE, Mikol J, Luccantoni-Freire S, Correia E, Lescoutra-Etchegaray N, Durand V, Dehen C, Andreoletti O, Casalone C, Richt JA, Greenlee JJ, Baron T, Benestad SL, Brown P, Deslys JP.

Sci Rep. 2015 Jun 30;5:11573. doi: 10.1038/srep11573.

16.

Transgenic fatal familial insomnia mice indicate prion infectivity-independent mechanisms of pathogenesis and phenotypic expression of disease.

Bouybayoune I, Mantovani S, Del Gallo F, Bertani I, Restelli E, Comerio L, Tapella L, Baracchi F, Fernández-Borges N, Mangieri M, Bisighini C, Beznoussenko GV, Paladini A, Balducci C, Micotti E, Forloni G, Castilla J, Fiordaliso F, Tagliavini F, Imeri L, Chiesa R.

PLoS Pathog. 2015 Apr 16;11(4):e1004796. doi: 10.1371/journal.ppat.1004796. Erratum in: PLoS Pathog. 2015 Jul;11(7):e1005046.

17.

Requirements for mutant and wild-type prion protein misfolding in vitro.

Noble GP, Walsh DJ, Miller MB, Jackson WS, Supattapone S.

Biochemistry. 2015 Feb 10;54(5):1180-7. doi: 10.1021/bi501495j.

18.

A study of clinical profile, radiological and electroencephalographic characteristics of suspected Creutzfeldt-Jakob disease in a tertiary care centre in South India.

Mahale RR, Javali M, Mehta A, Sharma S, Acharya P, Srinivasa R.

J Neurosci Rural Pract. 2015 Jan;6(1):39-50. doi: 10.4103/0976-3147.143189.

19.

Evaluation of the zoonotic potential of transmissible mink encephalopathy.

Comoy EE, Mikol J, Ruchoux MM, Durand V, Luccantoni-Freire S, Dehen C, Correia E, Casalone C, Richt JA, Greenlee JJ, Torres JM, Brown P, Deslys JP.

Pathogens. 2013 Jul 30;2(3):520-32. doi: 10.3390/pathogens2030520.

20.

Kuru: a journey back in time from papua new Guinea to the neanderthals' extinction.

Liberski PP.

Pathogens. 2013 Jul 18;2(3):472-505. doi: 10.3390/pathogens2030472. Review.

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