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B Ghetti

Showing results (191-200 of 227) with videos related to

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American Journal of Ophthalmology|April 1, 1997
Subacute sclerosing panencephalitis manifesting as viral retinitis: clinical and histopathologic findingsD W Park, H C Boldt, S J Massicotte, et al.
Nature Genetics|April 1, 1992
Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tanglesK Hsiao, S R Dlouhy, M R Farlow, 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 Neuropathology and Experimental Neurology|December 22, 1999
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal depositsJ R Murrell, M G Spillantini, P Zolo, et al.
Neurology|January 5, 2007
Clinicopathologic features of frontotemporal dementia with progranulin sequence variationS Spina, J R Murrell, E D Huey, et al.
Journal of Neuropathology and Experimental Neurology|January 5, 2002
Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizuresM Takao, B Ghetti, J R Murrell, et al.
Journal of Pediatric Surgery|October 24, 2022
Evaluating pediatric car safety compliance in motor vehicle collisions: Identifying high-risk groups for improper restraint usageClaudio B Ghetti, Alexandra S Rooney, Víctor de Cos, et al.
Neurology|August 24, 2005
Neuropsychological function in nondemented carriers of presenilin-1 mutationsJ M Ringman, C Diaz-Olavarrieta, Y Rodriguez, et al.
Annals of Neurology|September 8, 2000
Familial Alzheimer's disease: site of mutation influences clinical phenotypeC F Lippa, J M Swearer, K J Kane, et al.
Annals of Neurology|June 1, 1996
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob diseaseP Parchi, R Castellani, S Capellari, et al.
Pageof 23

Showing results (191-200 of 227) with videos related to

Sort By:
Pageof 23
American Journal of Ophthalmology|April 1, 1997
Subacute sclerosing panencephalitis manifesting as viral retinitis: clinical and histopathologic findingsD W Park, H C Boldt, S J Massicotte, et al.
Nature Genetics|April 1, 1992
Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tanglesK Hsiao, S R Dlouhy, M R Farlow, 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 Neuropathology and Experimental Neurology|December 22, 1999
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal depositsJ R Murrell, M G Spillantini, P Zolo, et al.
Neurology|January 5, 2007
Clinicopathologic features of frontotemporal dementia with progranulin sequence variationS Spina, J R Murrell, E D Huey, et al.
Journal of Neuropathology and Experimental Neurology|January 5, 2002
Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizuresM Takao, B Ghetti, J R Murrell, et al.
Journal of Pediatric Surgery|October 24, 2022
Evaluating pediatric car safety compliance in motor vehicle collisions: Identifying high-risk groups for improper restraint usageClaudio B Ghetti, Alexandra S Rooney, Víctor de Cos, et al.
Neurology|August 24, 2005
Neuropsychological function in nondemented carriers of presenilin-1 mutationsJ M Ringman, C Diaz-Olavarrieta, Y Rodriguez, et al.
Annals of Neurology|September 8, 2000
Familial Alzheimer's disease: site of mutation influences clinical phenotypeC F Lippa, J M Swearer, K J Kane, et al.
Annals of Neurology|June 1, 1996
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob diseaseP Parchi, R Castellani, S Capellari, et al.
Pageof 23