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Acta Neuropathologica|January 1, 1984

Experimental transmission of human subacute spongiform encephalopathy to small rodents. IV. Positive transmission from a typical case of Gerstmann-Sträussler-Scheinker's diseaseJ Tateishi, Y Sato, H Nagara, et al.

Acta Neuropathologica|January 1, 1980

Gerstmann-Sträussler-Scheinker's disease. Electron-microscopic observations on a brain biopsyW Schlote, J W Boellaard, F Schumm, et al.

Acta Neuropathologica|January 1, 1991

Neuronal autophagy in experimental scrapieJ W Boellaard, M Kao, W Schlote, et al.

Acta Neuropathologica|January 1, 1992

Creutzfeldt-Jakob disease with amyloid angiopathy: diagnosis by immunological analyses and transmission experimentsJ Tateishi, T Kitamoto, K Doh-ura, et al.

Neuropathology and Applied Neurobiology|February 1, 1990

Immunogold light and electron microscopic detection of amyloid plaques in transmissible spongiform encephalopathiesJ Doerr-Schott, T Kitamoto, J Tateishi, et al.

Acta Neuropathologica|January 1, 1993

Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndromeM Barcikowska, P P Liberski, J W Boellaard, et al.

Clinical Neuropathology|August 26, 1998

Gerstmann-Sträussler-Scheinker disease with A117V mutation in a second French-Alsatian familyN Heldt, J W Boellaard, P Brown, et al.

Virus Research|January 1, 2008

Tubulovesicular structures are a consistent (and unexplained) finding in the brains of humans with prion diseasesPawel P Liberski, Beata Sikorska, Jean-Jacques Hauw, et al.

Experimental Neurology|June 1, 1990

Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndromeL G Goldfarb, P Brown, D Goldgaber, et al.

Neurology|March 1, 1991

Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndromeP Brown, L G Goldfarb, W T Brown, et al.

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Showing results (11-20 of 20) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 20 results.

Acta Neuropathologica|January 1, 1984

Acta Neuropathologica|January 1, 1980

Gerstmann-Sträussler-Scheinker's disease. Electron-microscopic observations on a brain biopsyW Schlote, J W Boellaard, F Schumm, et al.

Acta Neuropathologica|January 1, 1991

Neuronal autophagy in experimental scrapieJ W Boellaard, M Kao, W Schlote, et al.

Acta Neuropathologica|January 1, 1992

Creutzfeldt-Jakob disease with amyloid angiopathy: diagnosis by immunological analyses and transmission experimentsJ Tateishi, T Kitamoto, K Doh-ura, et al.

Neuropathology and Applied Neurobiology|February 1, 1990

Immunogold light and electron microscopic detection of amyloid plaques in transmissible spongiform encephalopathiesJ Doerr-Schott, T Kitamoto, J Tateishi, et al.

Acta Neuropathologica|January 1, 1993

Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndromeM Barcikowska, P P Liberski, J W Boellaard, et al.

Clinical Neuropathology|August 26, 1998

Gerstmann-Sträussler-Scheinker disease with A117V mutation in a second French-Alsatian familyN Heldt, J W Boellaard, P Brown, et al.

Virus Research|January 1, 2008

Tubulovesicular structures are a consistent (and unexplained) finding in the brains of humans with prion diseasesPawel P Liberski, Beata Sikorska, Jean-Jacques Hauw, et al.

Experimental Neurology|June 1, 1990

Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndromeL G Goldfarb, P Brown, D Goldgaber, et al.

Neurology|March 1, 1991

Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndromeP Brown, L G Goldfarb, W T Brown, et al.

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