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Giorgio Giaccone

Showing results (81-90 of 129) with videos related to

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Frontiers in Neuroscience|July 14, 2020
Phospho-HDAC6 Gathers Into Protein Aggregates in Parkinson's Disease and Atypical ParkinsonismsSamanta Mazzetti, Mara De Leonardis, Gloria Gagliardi, et al.
Molecular Neurobiology|April 13, 2022
Serpin Signatures in Prion and Alzheimer's DiseasesMarco Zattoni, Marika Mearelli, Silvia Vanni, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 11, 2025
Transthyretin amyloid deposition in the ligamentum flavum of an Italian cohort of patients with lumbar spinal stenosisFrancesca Vitali, Silvia Fenu, Alessandro Izzo, et al.
Frontiers in Aging Neuroscience|December 26, 2022
Semantic and right temporal variant of FTD: Next generation sequencing genetic analysis on a single-center cohortGiacomina Rossi, Erika Salvi, Elkadia Mehmeti, et al.
European Journal of Neurology|July 5, 2022
SORL1 gene mutation and octapeptide repeat insertion in PRNP gene in a case presenting with rapidly progressive dementia and cerebral amyloid angiopathyFederica Cencini, Marcella Catania, Giuseppe Di Fede, et al.
Acta Neuropathologica|November 13, 2012
APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38Maria Luisa Moro, Giorgio Giaccone, Raffaella Lombardi, et al.
Brain Pathology (Zurich, Switzerland)|May 1, 2007
Effects of formalin fixation, paraffin embedding, and time of storage on DNA preservation in brain tissue: a BrainNet Europe studyIsidre Ferrer, Judith Armstrong, Sabina Capellari, et al.
Acta Neuropathologica|June 30, 2026
Prion-like transmission and propagation of human β-amyloid to the bank vole rodent modelMichele Angelo Di Bari, Rosalia Bruno, Geraldina Riccardi, et al.
Acta Neuropathologica|February 10, 2026
D178N prion protein mutation endows RML prions with new strain properties that do not mimic human genetic prion diseasesAntonio Masone, Anna Grasso, Liliana Comerio, et al.
Journal of Alzheimer'S Disease : JAD|October 5, 2020
The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman EmpireCinzia Coppola, Dario Saracino, Mariano Oliva, et al.
Pageof 13

Showing results (81-90 of 129) with videos related to

Sort By:
Pageof 13
Frontiers in Neuroscience|July 14, 2020
Phospho-HDAC6 Gathers Into Protein Aggregates in Parkinson's Disease and Atypical ParkinsonismsSamanta Mazzetti, Mara De Leonardis, Gloria Gagliardi, et al.
Molecular Neurobiology|April 13, 2022
Serpin Signatures in Prion and Alzheimer's DiseasesMarco Zattoni, Marika Mearelli, Silvia Vanni, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 11, 2025
Transthyretin amyloid deposition in the ligamentum flavum of an Italian cohort of patients with lumbar spinal stenosisFrancesca Vitali, Silvia Fenu, Alessandro Izzo, et al.
Frontiers in Aging Neuroscience|December 26, 2022
Semantic and right temporal variant of FTD: Next generation sequencing genetic analysis on a single-center cohortGiacomina Rossi, Erika Salvi, Elkadia Mehmeti, et al.
European Journal of Neurology|July 5, 2022
SORL1 gene mutation and octapeptide repeat insertion in PRNP gene in a case presenting with rapidly progressive dementia and cerebral amyloid angiopathyFederica Cencini, Marcella Catania, Giuseppe Di Fede, et al.
Acta Neuropathologica|November 13, 2012
APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38Maria Luisa Moro, Giorgio Giaccone, Raffaella Lombardi, et al.
Brain Pathology (Zurich, Switzerland)|May 1, 2007
Effects of formalin fixation, paraffin embedding, and time of storage on DNA preservation in brain tissue: a BrainNet Europe studyIsidre Ferrer, Judith Armstrong, Sabina Capellari, et al.
Acta Neuropathologica|June 30, 2026
Prion-like transmission and propagation of human β-amyloid to the bank vole rodent modelMichele Angelo Di Bari, Rosalia Bruno, Geraldina Riccardi, et al.
Acta Neuropathologica|February 10, 2026
D178N prion protein mutation endows RML prions with new strain properties that do not mimic human genetic prion diseasesAntonio Masone, Anna Grasso, Liliana Comerio, et al.
Journal of Alzheimer'S Disease : JAD|October 5, 2020
The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman EmpireCinzia Coppola, Dario Saracino, Mariano Oliva, et al.
Pageof 13