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F Tagliavini

Showing results (101-110 of 133) with videos related to

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Journal of Neuropathology and Experimental Neurology|November 1, 1995
Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165P Piccardo, B Ghetti, D W Dickson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 21, 2007
A novel phenotype of sporadic Creutzfeldt-Jakob diseaseG Giaccone, G Di Fede, M Mangieri, et al.
Neurology|April 1, 1998
Fatal familial insomnia: genetic, neuropathologic, and biochemical study of a patient from a new Italian kindredG Rossi, G Macchi, M Porro, et al.
The Biochemical Journal|December 1, 1996
Activation effects of a prion protein fragment [PrP-(106-126)] on human leucocytesL Diomede, S Sozzani, W Luini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 18, 2009
An atypical case of sporadic fatal insomniaL Priano, G Giaccone, M Mangieri, et al.
Neurobiology of Disease|December 15, 2000
Neurotoxicity of the putative transmembrane domain of the prion proteinS Haïk, J M Peyrin, L Lins, et al.
Neurobiology of Disease|August 31, 2000
Apoptotic cell death and impairment of L-type voltage-sensitive calcium channel activity in rat cerebellar granule cells treated with the prion protein fragment 106-126S Thellung, T Florio, V Villa, et al.
Journal of Neurology|June 1, 2012
Stereotypic behaviors in degenerative dementiasS Prioni, V Fetoni, F Barocco, et al.
Neurology|November 1, 1989
Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected familyB Ghetti, F Tagliavini, C L Masters, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2008
A novel insertional mutation in the prion protein gene: clinical and bio-molecular findingsC Mauro, G Giaccone, G Piscosquito, et al.
Pageof 14

Showing results (101-110 of 133) with videos related to

Sort By:
Pageof 14
Journal of Neuropathology and Experimental Neurology|November 1, 1995
Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165P Piccardo, B Ghetti, D W Dickson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 21, 2007
A novel phenotype of sporadic Creutzfeldt-Jakob diseaseG Giaccone, G Di Fede, M Mangieri, et al.
Neurology|April 1, 1998
Fatal familial insomnia: genetic, neuropathologic, and biochemical study of a patient from a new Italian kindredG Rossi, G Macchi, M Porro, et al.
The Biochemical Journal|December 1, 1996
Activation effects of a prion protein fragment [PrP-(106-126)] on human leucocytesL Diomede, S Sozzani, W Luini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 18, 2009
An atypical case of sporadic fatal insomniaL Priano, G Giaccone, M Mangieri, et al.
Neurobiology of Disease|December 15, 2000
Neurotoxicity of the putative transmembrane domain of the prion proteinS Haïk, J M Peyrin, L Lins, et al.
Neurobiology of Disease|August 31, 2000
Apoptotic cell death and impairment of L-type voltage-sensitive calcium channel activity in rat cerebellar granule cells treated with the prion protein fragment 106-126S Thellung, T Florio, V Villa, et al.
Journal of Neurology|June 1, 2012
Stereotypic behaviors in degenerative dementiasS Prioni, V Fetoni, F Barocco, et al.
Neurology|November 1, 1989
Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected familyB Ghetti, F Tagliavini, C L Masters, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2008
A novel insertional mutation in the prion protein gene: clinical and bio-molecular findingsC Mauro, G Giaccone, G Piscosquito, et al.
Pageof 14