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B Ghetti

Showing results (211-220 of 227) with videos related to

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Acta Neuropathologica|July 27, 2000
Senile dementia associated with amyloid beta protein angiopathy and tau perivascular pathology but not neuritic plaques in patients homozygous for the APOE-epsilon4 alleleR Vidal, M Calero, P Piccardo, 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.
Annals of Neurology|August 12, 1999
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjectsP Parchi, A Giese, S Capellari, et al.
Journal of Neuropathology and Experimental Neurology|April 28, 1999
Tau pathology in a family with dementia and a P301L mutation in tauS S Mirra, J R Murrell, M Gearing, 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.
Neurology|December 11, 2002
Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)Y Tsuboi, M Baker, M L Hutton, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|February 24, 2007
Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutationY Baba, M C Baker, I Le Ber, et al.
Neurology|February 13, 2002
Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob diseaseAna Lia Taratuto, P Piccardo, E G Reich, et al.
The American Journal of Pathology|November 12, 1998
Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genesC F Lippa, H Fujiwara, D M Mann, et al.
Pageof 23

Showing results (211-220 of 227) with videos related to

Sort By:
Pageof 23
Acta Neuropathologica|July 27, 2000
Senile dementia associated with amyloid beta protein angiopathy and tau perivascular pathology but not neuritic plaques in patients homozygous for the APOE-epsilon4 alleleR Vidal, M Calero, P Piccardo, 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.
Annals of Neurology|August 12, 1999
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjectsP Parchi, A Giese, S Capellari, et al.
Journal of Neuropathology and Experimental Neurology|April 28, 1999
Tau pathology in a family with dementia and a P301L mutation in tauS S Mirra, J R Murrell, M Gearing, 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.
Neurology|December 11, 2002
Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)Y Tsuboi, M Baker, M L Hutton, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|February 24, 2007
Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutationY Baba, M C Baker, I Le Ber, et al.
Neurology|February 13, 2002
Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob diseaseAna Lia Taratuto, P Piccardo, E G Reich, et al.
The American Journal of Pathology|November 12, 1998
Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genesC F Lippa, H Fujiwara, D M Mann, et al.
Pageof 23