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References
1.Creutzfeldt-Jakob disease surveillance in the United Kingdom . Edinburgh, UK : The National CJD Surveillance Unit , 1995 ;.
2.
Wells
GAH
Scott
AC
Johnson
CT
Gunning
RF
Hancock
RD
Jeffrey
M
Dawson
M
Bradley
R
. A novel progressive spongiform encephalopathy in cattle . Vet Rec
1987 ; 121 : 419 –420 .
3.
Palmer
MS
Dryden
AJ
Hughes
JT
Collinge
J
. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease . Nature
1991 : 352 : 340 –342 .
4.
Creutzfeldt
HG
. Uber eine eigenartige herdformige Ekrankung des Zentralnervensystems . Zeit Ncurol Psych
1920 ; 57 : 1 –18 .
5.
Kulczycki
J
Jedrzejowska
H
Gajkowski
K
Tarnowska-Dziduszko
E
Lojkowska
W
. Creutzfeldt-Jakob disease in voung people . Eur J lipid
1991 ; 7 : 501 –504 .
6.
Prusiner
SB
. Prion diseases of humans and animals . J Roy Coll Phy London
1994 ; 28 (Suppl ): 1 –30 .
7.
Brown
P
Goldfarb
LG
Gajdusek
DC
. The new biology of spongiform encephalopathy: infectious amyloidoses with a genetic twist . Lancet
1991 ; 337 : 1019 –1022 .
8.
Hsiao
KK
Groth
D
Scott
M
Yang
S-L
Scrban
H
Rapp
D
Foster
D
Torchia
M
DeArmond
SJ
Prusiner
SB
. Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein . Proc Natl Acad Sci USA
1994 ; 91 : 9126 –9130 .
9.
DeArmond
SJ
Prusiner
SB
. Prion protein transgenes and the neuropathology in prion diseases . Brain Pathology
1995 ; 5 : 77 –89 .
10.
Kocisko
DA
Come
JH
Priola
S
Chesebro
B
Raymond
GJ
Lansbury
PT
Caughey
B
. Cell-free formation of protease-resistant prion protein . Nature
1994 ; 370 : 471 –474 .
