The “brave new world” of transmissible spongiform encephalopathy (infectious cerebral amyloidosis) Paul Brown Neurodegenerative Diseases Pages: 79 - 87
Molecular genetic studies of Creutzfeldt-Jakob disease Lev G. GoldfarbPaul BrownD. Carleton Gajdusek Neurodegenerative Diseases Pages: 89 - 97
A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene) Robert B. PetersenLev G. GoldfarbPierluigi Gambeffi Neurodegenerative Diseases Pages: 99 - 103
PrP in pathology and pathogenesis in scrapie-infected mice M. E. BruceP. A. McBrideJ. R. Scott Neurodegenerative Diseases Pages: 105 - 112
Inhibition of scrapie-associated PrP accumulation Suzette A. PriolaByron Caughey Neurodegenerative Diseases Pages: 113 - 120
129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal J. C. MansonA. R. ClarkeJ. Hope Neurodegenerative Diseases Pages: 121 - 127
Scrapie strain infection in vitro induces changes in neuronal cells R. RubensteinH. DengR. Carp Neurodegenerative Diseases Pages: 129 - 138
The presence of HTLV-I proviral DNA in the central nervous system of patients with HTLV-I-associated myelopathy/tropical spastic paraparesis Jun-ichi Kira Neurodegenerative Diseases Pages: 139 - 145
HTLV-I, infective dermatitis, and tropical spastic paraparesis L. La Grenade Neurodegenerative Diseases Pages: 147 - 148
Genetic and phylogenetic analyses of human T-cell lymphotropic virus type I variants from Melanesians with an without spastic myelopathy Vivek R. NerurkarKi-Joon SongRichard Yanagihara Neurodegenerative Diseases Pages: 155 - 173
Tropical spastic paraparesis/HTLV-I associated myelopathy P. E. B. Rodgers-Johnson Neurodegenerative Diseases Pages: 175 - 179
