The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease

por Cordery, R, Alner, K, Cipolotti, L, Ron, M, Kennedy, A, Collinge, J, Rossor, M
Publicado em 2005

Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series

por Webb, T. E. F., Poulter, M., Beck, J., Uphill, J., Adamson, G., Campbell, T., Linehan, J., Powell, C., Brandner, S., Pal, S., Siddique, D., Wadsworth, J. D., Joiner, S., Alner, K., Petersen, C., Hampson, S., Rhymes, C., Treacy, C., Storey, E., Geschwind, M. D., Nemeth, A. H., Wroe, S., Collinge, J., Mead, S.
Publicado em 2008