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Items: 20

1.

Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob disease.

Choi EM, Geschwind MD, Deering C, Pomeroy K, Kuo A, Miller BL, Safar JG, Prusiner SB.

Lab Invest. 2009 Jun;89(6):624-35. doi: 10.1038/labinvest.2009.30.

2.

An overview of the diagnostic tools.

Coste J.

Transfus Clin Biol. 2013 Sep;20(4):412-5. doi: 10.1016/j.tracli.2013.04.110. Epub 2013 Aug 6. Review.

PMID:
23928182
3.

The cellular prion protein: biochemistry, topology, and physiologic functions.

Griffoni C, Toni M, Spisni E, Bianco M, Santi S, Riccio M, Tomasi V.

Cell Biochem Biophys. 2003;38(3):287-304. Review.

PMID:
12794269
4.

Prospects for the development of pre-mortem laboratory diagnostic tests for Creutzfeldt-Jakob disease.

Dabaghian RH, Mortimer PP, Clewley JP.

Rev Med Virol. 2004 Nov-Dec;14(6):345-61. Review.

PMID:
15495196
5.

Creutzfeldt-Jakob disease and scrapie prions.

Prusiner SB.

Alzheimer Dis Assoc Disord. 1989 Spring-Summer;3(1-2):52-78. Review.

PMID:
2568118
6.

Prion-induced neuronal damage--the mechanisms of neuronal destruction in the subacute spongiform encephalopathies.

Giese A, Kretzschmar HA.

Curr Top Microbiol Immunol. 2001;253:203-17. Review.

PMID:
11417136
7.

Synaptic pathology and cell death in the cerebellum in Creutzfeldt-Jakob disease.

Ferrer I.

Cerebellum. 2002 Jul;1(3):213-22. Review.

PMID:
12879983
8.

Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews.

Meiner Z, Gabizon R, Prusiner SB.

Medicine (Baltimore). 1997 Jul;76(4):227-37. Review.

9.

Prion diseases and the BSE crisis.

Prusiner SB.

Science. 1997 Oct 10;278(5336):245-51. Review.

PMID:
9323196
10.

Genetic and infectious prion diseases.

Prusiner SB.

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

PMID:
8105771
11.

On the biology of prions.

Prusiner SB, Gabizon R, McKinley MP.

Acta Neuropathol. 1987;72(4):299-314. Review.

PMID:
3554880
12.

Biochemical and strain properties of CJD prions: complexity versus simplicity.

Haïk S, Brandel JP.

J Neurochem. 2011 Oct;119(2):251-61. doi: 10.1111/j.1471-4159.2011.07399.x. Epub 2011 Sep 20. Review.

13.

Prion protein and developments in its detection.

MacGregor I.

Transfus Med. 2001 Feb;11(1):3-14. Review.

PMID:
11328566
14.

Novel mechanisms of degeneration of the central nervous system--prion structure and biology.

Prusiner SB, Stahl N, DeArmond SJ.

Ciba Found Symp. 1988;135:239-60. Review.

PMID:
2900720
15.

[Functions of prion protein PrPc].

Cazaubon S, Viegas P, Couraud PO.

Med Sci (Paris). 2007 Aug-Sep;23(8-9):741-5. Review. French.

16.

Emerging pharmacotherapies for Creutzfeldt-Jakob disease.

Korth C, Peters PJ.

Arch Neurol. 2006 Apr;63(4):497-501. Review.

PMID:
16606761
17.

Update on Creutzfeldt-Jakob disease.

Mallucci G, Collinge J.

Curr Opin Neurol. 2004 Dec;17(6):641-7. Review.

PMID:
15542971
18.

Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia.

Gambetti P, Parchi P, Chen SG.

Clin Lab Med. 2003 Mar;23(1):43-64. Review.

PMID:
12733424
19.

Variant Creutzfeldt-Jakob disease and its transmission by blood.

Ironside JW, Head MW.

J Thromb Haemost. 2003 Jul;1(7):1479-86. Review.

20.

Obstetric dilemma on the most appropriate management of Creutzfeldt-Jakob disease in pregnancy: seventh case presentation, literature review and new insight.

Di Gangi S, Bertin M, Noventa M, Cagnin A, Cosmi E, Gizzo S.

J Matern Fetal Neonatal Med. 2015 Feb;28(3):254-61. doi: 10.3109/14767058.2014.916678. Epub 2014 May 27. Review.

PMID:
24749800
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