Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Piccardo

Showing results (21-30 of 58) with videos related to

Pageof 6
Sort By:
Journal of Neuropathology and Experimental Neurology|February 24, 2001
Codeposition of cystatin C with amyloid-beta protein in the brain of Alzheimer disease patientsE Levy, M Sastre, A Kumar, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2000
Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutationR Chiesa, B Drisaldi, E Quaglio, et al.
Journal of Neurocytology|August 1, 1995
Alz-50 recognizes epitopes in primary sensory fibres and in neurons of the substantia gelatinosa of the spinal cord. An ultrastructural study in the ratP Liberini, P Piccardo, W Ma, et al.
Archives of Virology. Supplementum|February 24, 2001
A transgenic model of a familial prion diseaseD A Harris, R Chiesa, B Drisaldi, et al.
Annals of Neurology|January 1, 1988
HTLV-I-like viral particles in spinal cord cells in Jamaican tropical spastic paraparesisP P Liberski, P Rodgers-Johnson, G Char, et al.
Neurology|July 1, 1986
Neuropathologic verification of Creutzfeldt-Jakob disease in the exhumed American recipient of human pituitary growth hormone: epidemiologic and pathogenetic implicationsR Tintner, P Brown, E T Hedley-Whyte, et al.
Neurology|March 11, 1990
Subcellular distribution and physicochemical properties of scrapie-associated precursor protein and relationship with scrapie agentJ Safar, M Ceroni, P Piccardo, et al.
Neurobiology of Disease|April 13, 2001
Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutationR Chiesa, A Pestronk, R E Schmidt, et al.
The American Journal of Pathology|November 12, 1998
Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissuesA Jiménez-Huete, P M Lievens, R Vidal, et al.
Annals of Neurology|January 1, 1988
Intrathecal synthesis of IgG antibodies to HTLV-I supports an etiological role for HTLV-I in tropical spastic paraparesisM Ceroni, P Piccardo, P Rodgers-Johnson, et al.
Pageof 6

Showing results (21-30 of 58) with videos related to

Sort By:
Pageof 6
Journal of Neuropathology and Experimental Neurology|February 24, 2001
Codeposition of cystatin C with amyloid-beta protein in the brain of Alzheimer disease patientsE Levy, M Sastre, A Kumar, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2000
Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutationR Chiesa, B Drisaldi, E Quaglio, et al.
Journal of Neurocytology|August 1, 1995
Alz-50 recognizes epitopes in primary sensory fibres and in neurons of the substantia gelatinosa of the spinal cord. An ultrastructural study in the ratP Liberini, P Piccardo, W Ma, et al.
Archives of Virology. Supplementum|February 24, 2001
A transgenic model of a familial prion diseaseD A Harris, R Chiesa, B Drisaldi, et al.
Annals of Neurology|January 1, 1988
HTLV-I-like viral particles in spinal cord cells in Jamaican tropical spastic paraparesisP P Liberski, P Rodgers-Johnson, G Char, et al.
Neurology|July 1, 1986
Neuropathologic verification of Creutzfeldt-Jakob disease in the exhumed American recipient of human pituitary growth hormone: epidemiologic and pathogenetic implicationsR Tintner, P Brown, E T Hedley-Whyte, et al.
Neurology|March 11, 1990
Subcellular distribution and physicochemical properties of scrapie-associated precursor protein and relationship with scrapie agentJ Safar, M Ceroni, P Piccardo, et al.
Neurobiology of Disease|April 13, 2001
Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutationR Chiesa, A Pestronk, R E Schmidt, et al.
The American Journal of Pathology|November 12, 1998
Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissuesA Jiménez-Huete, P M Lievens, R Vidal, et al.
Annals of Neurology|January 1, 1988
Intrathecal synthesis of IgG antibodies to HTLV-I supports an etiological role for HTLV-I in tropical spastic paraparesisM Ceroni, P Piccardo, P Rodgers-Johnson, et al.
Pageof 6