New diagnostic tests for prion diseases

[1] BATEMAN D, 1995, LANCET, V346, P1155, DOI 10.1016/S0140-6736(95)91828-0

[2] SPORADIC CREUTZFELDT-JAKOB-DISEASE IN A 16-YEAR-OLD IN THE UK [J]. LANCET, 1995, 346 (8983): : 1155 - 1155

[3] TRANSMISSION OF BOVINE SPONGIFORM ENCEPHALOPATHY AND SCRAPIE TO MICE - STRAIN VARIATION AND THE SPECIES BARRIER [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1994, 343 (1306) : 405 - 411

[4] New variant of Creutzfeldt-Jakob disease in a 26-year-old French man [J]. LANCET, 1996, 347 (9009) : 1181 - 1181

[5] DIAGNOSIS OF GERSTMANN-STRAUSSLER SYNDROME IN FAMILIAL DEMENTIA WITH PRION PROTEIN GENE ANALYSIS [J]. LANCET, 1989, 2 (8653) : 15 - 17

[6] INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION .2. CLINICAL AND PATHOLOGICAL FEATURES [J]. BRAIN, 1992, 115 : 687 - 710

[7] COLLINGE J, 1991, AM J HUM GENET, V49, P1351

[8] GENETIC PREDISPOSITION TO IATROGENIC CREUTZFELDT-JAKOB DISEASE [J]. LANCET, 1991, 337 (8755) : 1441 - 1442

[9] UNALTERED SUSCEPTIBILITY TO BSE IN TRANSGENIC MICE EXPRESSING HUMAN PRION PROTEIN [J]. NATURE, 1995, 378 (6559) : 779 - 783

[10] PRION PROTEIN IS NECESSARY FOR NORMAL SYNAPTIC FUNCTION [J]. NATURE, 1994, 370 (6487) : 295 - 297

[1] BATEMAN D, 1995, LANCET, V346, P1155, DOI 10.1016/S0140-6736(95)91828-0

[2] SPORADIC CREUTZFELDT-JAKOB-DISEASE IN A 16-YEAR-OLD IN THE UK [J]. LANCET, 1995, 346 (8983): : 1155 - 1155

[3] TRANSMISSION OF BOVINE SPONGIFORM ENCEPHALOPATHY AND SCRAPIE TO MICE - STRAIN VARIATION AND THE SPECIES BARRIER [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1994, 343 (1306) : 405 - 411

[4] New variant of Creutzfeldt-Jakob disease in a 26-year-old French man [J]. LANCET, 1996, 347 (9009) : 1181 - 1181

[5] DIAGNOSIS OF GERSTMANN-STRAUSSLER SYNDROME IN FAMILIAL DEMENTIA WITH PRION PROTEIN GENE ANALYSIS [J]. LANCET, 1989, 2 (8653) : 15 - 17

[6] INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION .2. CLINICAL AND PATHOLOGICAL FEATURES [J]. BRAIN, 1992, 115 : 687 - 710

[7] COLLINGE J, 1991, AM J HUM GENET, V49, P1351

[8] GENETIC PREDISPOSITION TO IATROGENIC CREUTZFELDT-JAKOB DISEASE [J]. LANCET, 1991, 337 (8755) : 1441 - 1442

[9] UNALTERED SUSCEPTIBILITY TO BSE IN TRANSGENIC MICE EXPRESSING HUMAN PRION PROTEIN [J]. NATURE, 1995, 378 (6559) : 779 - 783

[10] PRION PROTEIN IS NECESSARY FOR NORMAL SYNAPTIC FUNCTION [J]. NATURE, 1994, 370 (6487) : 295 - 297