M Pocchiari

Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.

P Brown, J. Long, H. Budka, 1999, American journal of human genetics.

Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease.

J Mackenzie, H. Budka, G. Jansen, 2006, Brain : a journal of neurology.

Highly infectious purified preparations of disease-specific amyloid of transmissible spongiform encephalopathies are not devoid of nucleic acids of viral size.

M. Beekes, J. Ironside, M. Pocchiari, 1997, Intervirology.

Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt–Jakob disease

H. Budka, J. Laplanche, H. Bernheimer, 2000, Neurology.