Author:
Gambetti Pierluigi,Cali Ignazio
Publisher
Springer International Publishing
Reference65 articles.
1. Alema G, Bignami A. Subacute degenerative presenile polioencephalopathy with akinetic stupor and decorticate rigidity with myoclonus (“myoclonic” variety of the Jakob-Creutzfeld disease). Riv Sper Freniatr Med Leg Alien Ment. 1959;83((4)Suppl):1485–623.
2. Appleby BS, Maddox R, Schonberger LB, Cali I, Hammett T, Cohen M, Belay E. Sporadic Creutzfeldt-Jakob disease in a very young person. Neurology. 2021;97:813–6. https://doi.org/10.1212/wnl.0000000000012737.
3. Baiardi S, Rossi M, Capellari S, Parchi P. Recent advances in the histo-molecular pathology of human prion disease. Brain Pathol. 2019;29:278–300. https://doi.org/10.1111/bpa.12695.
4. Bartz JC. Environmental and host factors that contribute to prion strain evolution. Acta Neuropathol. 2021;142:5–16. https://doi.org/10.1007/s00401-021-02310-6.
5. Berghoff AS, Trummert A, Unterberger U, Ströbel T, Hortobágyi T, Kovacs GG. Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease. Neuropathology. 2015;35:336–42. https://doi.org/10.1111/neup.12192.
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