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Giorgio Giaccone

Showing results (31-40 of 129) with videos related to

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European Journal of Neurology|January 12, 2022
MAPT Q336H mutation: Intrafamilial phenotypic heterogeneity in a new Italian familyCristina Villa, Giacomina Rossi, Ilaria Bizzozero, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 3, 2017
Towards an early clinical diagnosis of sporadic CJD VV2 (ataxic type)Simone Baiardi, Anna Magherini, Sabina Capellari, et al.
Journal of Alzheimer'S Disease : JAD|June 17, 2011
Variability of the clinical phenotype in an Italian family with dementia associated with an intronic deletion in the GRN geneGabriella Marcon, Giacomina Rossi, Giorgio Giaccone, et al.
Journal of Neuropathology and Experimental Neurology|April 2, 2004
Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 geneGabriella Marcon, Giorgio Giaccone, Chiara Cupidi, et al.
Neurobiology of Aging|December 16, 2019
One novel GRN null mutation, two different aphasia phenotypesCinzia Coppola, Mariano Oliva, Dario Saracino, et al.
Scientific Reports|December 11, 2019
Use of different RT-QuIC substrates for detecting CWD prions in the brain of Norwegian cervidsEdoardo Bistaffa, Tram Thu Vuong, Federico Angelo Cazzaniga, et al.
Journal of Alzheimer'S Disease : JAD|December 25, 2014
Prodromal Alzheimer's disease presenting as cerebral amyloid angiopathy-related inflammation with spontaneous amyloid-related imaging abnormalities and high cerebrospinal fluid anti-Aβ autoantibodiesGiorgio B Boncoraglio, Fabrizio Piazza, Mario Savoiardo, et al.
International Journal of Molecular Sciences|November 26, 2022
Pathological 25 kDa C-Terminal Fragments of TDP-43 Are Present in Lymphoblastoid Cell Lines and Extracellular Vesicles from Patients Affected by Frontotemporal Lobar Degeneration and Neuronal Ceroidolipofuscinosis Carrying a <i>GRN</i> MutationSara Cimini, Sonia Bellini, Claudia Saraceno, et al.
Journal of Neuropathology and Experimental Neurology|February 7, 2007
The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker diseaseGiuseppe Di Fede, Giorgio Giaccone, Lucia Limido, et al.
Neurobiology of Aging|March 14, 2017
Missense mutation in GRN gene affecting RNA splicing and plasma progranulin level in a family affected by frontotemporal lobar degenerationSimona Luzzi, Lara Colleoni, Paola Corbetta, et al.
Pageof 13

Showing results (31-40 of 129) with videos related to

Sort By:
Pageof 13
European Journal of Neurology|January 12, 2022
MAPT Q336H mutation: Intrafamilial phenotypic heterogeneity in a new Italian familyCristina Villa, Giacomina Rossi, Ilaria Bizzozero, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 3, 2017
Towards an early clinical diagnosis of sporadic CJD VV2 (ataxic type)Simone Baiardi, Anna Magherini, Sabina Capellari, et al.
Journal of Alzheimer'S Disease : JAD|June 17, 2011
Variability of the clinical phenotype in an Italian family with dementia associated with an intronic deletion in the GRN geneGabriella Marcon, Giacomina Rossi, Giorgio Giaccone, et al.
Journal of Neuropathology and Experimental Neurology|April 2, 2004
Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 geneGabriella Marcon, Giorgio Giaccone, Chiara Cupidi, et al.
Neurobiology of Aging|December 16, 2019
One novel GRN null mutation, two different aphasia phenotypesCinzia Coppola, Mariano Oliva, Dario Saracino, et al.
Scientific Reports|December 11, 2019
Use of different RT-QuIC substrates for detecting CWD prions in the brain of Norwegian cervidsEdoardo Bistaffa, Tram Thu Vuong, Federico Angelo Cazzaniga, et al.
Journal of Alzheimer'S Disease : JAD|December 25, 2014
Prodromal Alzheimer's disease presenting as cerebral amyloid angiopathy-related inflammation with spontaneous amyloid-related imaging abnormalities and high cerebrospinal fluid anti-Aβ autoantibodiesGiorgio B Boncoraglio, Fabrizio Piazza, Mario Savoiardo, et al.
International Journal of Molecular Sciences|November 26, 2022
Pathological 25 kDa C-Terminal Fragments of TDP-43 Are Present in Lymphoblastoid Cell Lines and Extracellular Vesicles from Patients Affected by Frontotemporal Lobar Degeneration and Neuronal Ceroidolipofuscinosis Carrying a <i>GRN</i> MutationSara Cimini, Sonia Bellini, Claudia Saraceno, et al.
Journal of Neuropathology and Experimental Neurology|February 7, 2007
The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker diseaseGiuseppe Di Fede, Giorgio Giaccone, Lucia Limido, et al.
Neurobiology of Aging|March 14, 2017
Missense mutation in GRN gene affecting RNA splicing and plasma progranulin level in a family affected by frontotemporal lobar degenerationSimona Luzzi, Lara Colleoni, Paola Corbetta, et al.
Pageof 13