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

Gabriella Marcon

Showing results (21-30 of 38) with videos related to

Pageof 4
Sort By:
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.
Journal of Neurology|June 9, 2005
Familial frontotemporal dementia associated with the novel MAPT mutation T427MGiorgio Giaccone, Giacomina Rossi, Laura Farina, et al.
Free Radical Research|March 8, 2008
APE1/Ref-1 regulates PTEN expression mediated by Egr-1Damiano Fantini, Carlo Vascotto, Marta Deganuto, et al.
International Journal of Cardiology|July 11, 2016
Risk of dementia and death in patients with atrial fibrillation: A competing risk analysis of a population-based cohortIrene Marzona, Marta Baviera, Tommaso Vannini, et al.
Clinical Nutrition (Edinburgh, Scotland)|July 9, 2021
The role of diet on the risk of dementia in the oldest old: The Monzino 80-plus population-based studyCristina Nicoli, Alessia Antonella Galbussera, Cristina Bosetti, et al.
Brain Pathology (Zurich, Switzerland)|October 15, 2013
Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein GeneGabriella Marcon, Antonio Indaco, Giuseppe Di Fede, et al.
Neurobiology of Aging|May 19, 2024
Region-specific and age-related differences in astrocytes in the human brainJodie H K Man, Marjolein Breur, Charlotte A G H van Gelder, et al.
Mediators of Inflammation|October 31, 2017
Amyotrophic Lateral Sclerosis, a Multisystem Pathology: Insights into the Role of TNF<i>α</i>Massimo Tortarolo, Daniele Lo Coco, Pietro Veglianese, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|June 11, 2020
Echocardiographic evaluation of centenarians in TriesteAntonio Cannatà, Piero Gentile, Alessia Paldino, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
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.
Journal of Neurology|June 9, 2005
Familial frontotemporal dementia associated with the novel MAPT mutation T427MGiorgio Giaccone, Giacomina Rossi, Laura Farina, et al.
Free Radical Research|March 8, 2008
APE1/Ref-1 regulates PTEN expression mediated by Egr-1Damiano Fantini, Carlo Vascotto, Marta Deganuto, et al.
International Journal of Cardiology|July 11, 2016
Risk of dementia and death in patients with atrial fibrillation: A competing risk analysis of a population-based cohortIrene Marzona, Marta Baviera, Tommaso Vannini, et al.
Clinical Nutrition (Edinburgh, Scotland)|July 9, 2021
The role of diet on the risk of dementia in the oldest old: The Monzino 80-plus population-based studyCristina Nicoli, Alessia Antonella Galbussera, Cristina Bosetti, et al.
Brain Pathology (Zurich, Switzerland)|October 15, 2013
Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein GeneGabriella Marcon, Antonio Indaco, Giuseppe Di Fede, et al.
Neurobiology of Aging|May 19, 2024
Region-specific and age-related differences in astrocytes in the human brainJodie H K Man, Marjolein Breur, Charlotte A G H van Gelder, et al.
Mediators of Inflammation|October 31, 2017
Amyotrophic Lateral Sclerosis, a Multisystem Pathology: Insights into the Role of TNF<i>α</i>Massimo Tortarolo, Daniele Lo Coco, Pietro Veglianese, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|June 11, 2020
Echocardiographic evaluation of centenarians in TriesteAntonio Cannatà, Piero Gentile, Alessia Paldino, et al.
Pageof 4