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F Tagliavini

Showing results (121-130 of 133) with videos related to

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Neurology|March 2, 2011
Anti-Aβ autoantibodies in the CSF of a patient with CAA-related inflammation: a case reportJ C DiFrancesco, M Brioschi, L Brighina, et al.
Neurology|September 15, 2004
A family with Alzheimer disease and strokes associated with A713T mutation of the APP geneG Rossi, G Giaccone, R Maletta, et al.
The Journal of Biological Chemistry|November 23, 2000
A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117VF Tagliavini, P M Lievens, C Tranchant, et al.
The American Journal of Pathology|January 1, 1996
beta PP and Tau interaction. A possible link between amyloid and neurofibrillary tangles in Alzheimer's diseaseG Giaccone, B Pedrotti, A Migheli, et al.
Scientific Reports|November 17, 2017
Differential overexpression of SERPINA3 in human prion diseasesS Vanni, F Moda, M Zattoni, et al.
Journal of Neuropathology and Experimental Neurology|June 22, 1999
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tauO Bugiani, J R Murrell, G Giaccone, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 23, 1996
Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNPB Ghetti, P Piccardo, M G Spillantini, et al.
Journal of Virology|July 15, 2003
Evaluation of quinacrine treatment for prion diseasesA Barret, F Tagliavini, G Forloni, et al.
The American Journal of Pathology|June 8, 2001
Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutationsP Piccardo, J J Liepnieks, A William, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 22, 2014
Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in ItalyB Borroni, R Turrone, D Galimberti, et al.
Pageof 14

Showing results (121-130 of 133) with videos related to

Sort By:
Pageof 14
Neurology|March 2, 2011
Anti-Aβ autoantibodies in the CSF of a patient with CAA-related inflammation: a case reportJ C DiFrancesco, M Brioschi, L Brighina, et al.
Neurology|September 15, 2004
A family with Alzheimer disease and strokes associated with A713T mutation of the APP geneG Rossi, G Giaccone, R Maletta, et al.
The Journal of Biological Chemistry|November 23, 2000
A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117VF Tagliavini, P M Lievens, C Tranchant, et al.
The American Journal of Pathology|January 1, 1996
beta PP and Tau interaction. A possible link between amyloid and neurofibrillary tangles in Alzheimer's diseaseG Giaccone, B Pedrotti, A Migheli, et al.
Scientific Reports|November 17, 2017
Differential overexpression of SERPINA3 in human prion diseasesS Vanni, F Moda, M Zattoni, et al.
Journal of Neuropathology and Experimental Neurology|June 22, 1999
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tauO Bugiani, J R Murrell, G Giaccone, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 23, 1996
Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNPB Ghetti, P Piccardo, M G Spillantini, et al.
Journal of Virology|July 15, 2003
Evaluation of quinacrine treatment for prion diseasesA Barret, F Tagliavini, G Forloni, et al.
The American Journal of Pathology|June 8, 2001
Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutationsP Piccardo, J J Liepnieks, A William, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 22, 2014
Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in ItalyB Borroni, R Turrone, D Galimberti, et al.
Pageof 14