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Showing results (111-120 of 138) with videos related to

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Journal of Neuropathology and Experimental Neurology|November 1, 1996
Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred)P Piccardo, C Seiler, S R Dlouhy, et al.
Cell|November 18, 1994
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant alleleF Tagliavini, F Prelli, M Porro, et al.
Brain Pathology (Zurich, Switzerland)|July 1, 1995
Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)H Budka, A Aguzzi, P Brown, et al.
Brain Research|July 9, 1993
A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindredF Tagliavini, G Giaccone, F Prelli, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 29, 2005
FVEPs in Creutzfeldt-Jacob disease: waveforms and interaction with the periodic EEG pattern assessed by single sweep analysisE Visani, P Agazzi, V Scaioli, 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.
Brain Pathology (Zurich, Switzerland)|October 1, 1995
Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)H Budka, A Aguzzi, P Brown, et al.
Nature Medicine|April 1, 1995
Tau protein directly interacts with the amyloid beta-protein precursor: implications for Alzheimer's diseaseM A Smith, S L Siedlak, P L Richey, et al.
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.
Pageof 14

Showing results (111-120 of 138) with videos related to

Sort By:
Pageof 14
Journal of Neuropathology and Experimental Neurology|November 1, 1996
Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred)P Piccardo, C Seiler, S R Dlouhy, et al.
Cell|November 18, 1994
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant alleleF Tagliavini, F Prelli, M Porro, et al.
Brain Pathology (Zurich, Switzerland)|July 1, 1995
Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)H Budka, A Aguzzi, P Brown, et al.
Brain Research|July 9, 1993
A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindredF Tagliavini, G Giaccone, F Prelli, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 29, 2005
FVEPs in Creutzfeldt-Jacob disease: waveforms and interaction with the periodic EEG pattern assessed by single sweep analysisE Visani, P Agazzi, V Scaioli, 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.
Brain Pathology (Zurich, Switzerland)|October 1, 1995
Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases)H Budka, A Aguzzi, P Brown, et al.
Nature Medicine|April 1, 1995
Tau protein directly interacts with the amyloid beta-protein precursor: implications for Alzheimer's diseaseM A Smith, S L Siedlak, P L Richey, et al.
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.
Pageof 14