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Fabrizio Gardoni

Showing results (131-140 of 139) with videos related to

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Brain : a Journal of Neurology|May 8, 2012
Mechanisms underlying the impairment of hippocampal long-term potentiation and memory in experimental Parkinson's diseaseCinzia Costa, Carmelo Sgobio, Sabrina Siliquini, et al.
Brain, Behavior, and Immunity|March 14, 2024
Anti-GluA3 autoantibodies define a new sub-population of frontotemporal lobar degeneration patients with distinct neuropathological featuresMaria Italia, Michela Salvadè, Filippo La Greca, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 16, 2016
Coxsackievirus Adenovirus Receptor Loss Impairs Adult Neurogenesis, Synapse Content, and Hippocampus PlasticityCharleine Zussy, Fabien Loustalot, Felix Junyent, et al.
Brain : a Journal of Neurology|March 31, 2019
Alpha-synuclein targets GluN2A NMDA receptor subunit causing striatal synaptic dysfunction and visuospatial memory alterationValentina Durante, Antonio de Iure, Vittorio Loffredo, et al.
Pharmacological Research|February 14, 2025
Neuronal PCSK9 regulates cognitive performances via the modulation of ApoER2 synaptic localizationSilvia Pelucchi, Lorenzo Da Dalt, Giulia De Cesare, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 1, 2023
Detection of TDP-43 seeding activity in the olfactory mucosa from patients with frontotemporal dementiaElena Fontana, Matilde Bongianni, Alberto Benussi, et al.
Biological Psychiatry|September 23, 2015
Alpha-Synuclein Produces Early Behavioral Alterations via Striatal Cholinergic Synaptic Dysfunction by Interacting With GluN2D N-Methyl-D-Aspartate Receptor SubunitAlessandro Tozzi, Antonio de Iure, Vincenza Bagetta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 5, 2023
Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorderLisa Pavinato, Jennifer Stanic, Marta Barzasi, et al.
Progress in Neurobiology|July 26, 2015
Pathophysiology of L-dopa-induced motor and non-motor complications in Parkinson's diseaseMatthieu F Bastide, Wassilios G Meissner, Barbara Picconi, et al.
Pageof 14

Showing results (131-140 of 139) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 139 results.
Brain : a Journal of Neurology|May 8, 2012
Mechanisms underlying the impairment of hippocampal long-term potentiation and memory in experimental Parkinson's diseaseCinzia Costa, Carmelo Sgobio, Sabrina Siliquini, et al.
Brain, Behavior, and Immunity|March 14, 2024
Anti-GluA3 autoantibodies define a new sub-population of frontotemporal lobar degeneration patients with distinct neuropathological featuresMaria Italia, Michela Salvadè, Filippo La Greca, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 16, 2016
Coxsackievirus Adenovirus Receptor Loss Impairs Adult Neurogenesis, Synapse Content, and Hippocampus PlasticityCharleine Zussy, Fabien Loustalot, Felix Junyent, et al.
Brain : a Journal of Neurology|March 31, 2019
Alpha-synuclein targets GluN2A NMDA receptor subunit causing striatal synaptic dysfunction and visuospatial memory alterationValentina Durante, Antonio de Iure, Vittorio Loffredo, et al.
Pharmacological Research|February 14, 2025
Neuronal PCSK9 regulates cognitive performances via the modulation of ApoER2 synaptic localizationSilvia Pelucchi, Lorenzo Da Dalt, Giulia De Cesare, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 1, 2023
Detection of TDP-43 seeding activity in the olfactory mucosa from patients with frontotemporal dementiaElena Fontana, Matilde Bongianni, Alberto Benussi, et al.
Biological Psychiatry|September 23, 2015
Alpha-Synuclein Produces Early Behavioral Alterations via Striatal Cholinergic Synaptic Dysfunction by Interacting With GluN2D N-Methyl-D-Aspartate Receptor SubunitAlessandro Tozzi, Antonio de Iure, Vincenza Bagetta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 5, 2023
Missense variants in RPH3A cause defects in excitatory synaptic function and are associated with a clinically variable neurodevelopmental disorderLisa Pavinato, Jennifer Stanic, Marta Barzasi, et al.
Progress in Neurobiology|July 26, 2015
Pathophysiology of L-dopa-induced motor and non-motor complications in Parkinson's diseaseMatthieu F Bastide, Wassilios G Meissner, Barbara Picconi, et al.
Pageof 14