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Items: 10

1.

Diagnosis of human prion disease.

Safar JG, Geschwind MD, Deering C, Didorenko S, Sattavat M, Sanchez H, Serban A, Vey M, Baron H, Giles K, Miller BL, Dearmond SJ, Prusiner SB.

Proc Natl Acad Sci U S A. 2005 Mar 1;102(9):3501-6.

2.

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
3.

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.

4.

Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease.

Ironside JW, Head MW.

Curr Top Microbiol Immunol. 2004;284:133-59. Review.

PMID:
15148991
5.

Creutzfeldt-Jakob disease: updated diagnostic criteria, treatment algorithm, and the utility of brain biopsy.

Manix M, Kalakoti P, Henry M, Thakur J, Menger R, Guthikonda B, Nanda A.

Neurosurg Focus. 2015 Nov;39(5):E2. doi: 10.3171/2015.8.FOCUS15328. Review.

PMID:
26646926
6.

Molecular diagnostic tools in Creutzfeldt-Jakob disease and other prion disorders.

Van Everbroeck B, Boons J, De Leenheir E, L├╝bke U, Cras P.

Expert Rev Mol Diagn. 2004 May;4(3):351-9. Review.

PMID:
15137902
7.

Pathological diagnosis of variant Creutzfeldt-Jakob disease.

Ironside JW, McCardle L, Horsburgh A, Lim Z, Head MW.

APMIS. 2002 Jan;110(1):79-87. Review.

PMID:
12064259
8.

Sporadic and familial CJD: classification and characterisation.

Gambetti P, Kong Q, Zou W, Parchi P, Chen SG.

Br Med Bull. 2003;66:213-39. Review.

PMID:
14522861
9.

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

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