APA

Faucheux B. A., Morain E., Diouron V., Brandel J., Salomon D., Sazdovitch V., Privat N., Laplanche J., Hauw J. & Haïk S. (20111107). Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes. : Neuropathology and applied neurobiology.

Chicago

Faucheux B A, Morain E, Diouron V, Brandel J-P, Salomon D, Sazdovitch V, Privat N, Laplanche J-L, Hauw J-J and Haïk S. 20111107. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes. : Neuropathology and applied neurobiology.

Harvard

Faucheux B. A., Morain E., Diouron V., Brandel J., Salomon D., Sazdovitch V., Privat N., Laplanche J., Hauw J. and Haïk S. (20111107). Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes. : Neuropathology and applied neurobiology.

MLA

Faucheux B A, Morain E, Diouron V, Brandel J-P, Salomon D, Sazdovitch V, Privat N, Laplanche J-L, Hauw J-J and Haïk S. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes. : Neuropathology and applied neurobiology. 20111107.