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Showing results (161-170 of 199) with videos related to

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Neurobiology of Aging|May 21, 2005
The effects of APOE and tau gene variability on risk of frontotemporal dementiaL Bernardi, R G Maletta, C Tomaino, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 8, 2011
Position paper of the Italian Society for the study of Dementias (SINDEM) on the proposal of a new lexicon on Alzheimer diseaseMassimo Musicco, Alessandro Padovani, Sandro Sorbi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 22, 2014
Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in ItalyB Borroni, R Turrone, D Galimberti, et al.
Neurogenetics|November 21, 2001
Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's diseaseM Nicolaou, Y Q Song, C A Sato, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 18, 2020
Early diagnosis of Alzheimer's disease: the role of biomarkers including advanced EEG signal analysis. Report from the IFCN-sponsored panel of expertsP M Rossini, R Di Iorio, F Vecchio, et al.
Frontiers in Aging Neuroscience|May 10, 2021
Being the Family Caregiver of a Patient With Dementia During the Coronavirus Disease 2019 LockdownMilena Zucca, Valeria Isella, Raffaele Di Lorenzo, et al.
Journal of Alzheimer'S Disease : JAD|March 23, 2011
A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological featuresMaura Gallo, Norina Marcello, Sabrina A M Curcio, et al.
Human Molecular Genetics|June 9, 2014
Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patientsZhengrui Xi, Innocenzo Rainero, Elisa Rubino, et al.
Neurology|May 8, 2015
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease familyMaria E Conidi, Livia Bernardi, Gianfranco Puccio, et al.
Journal of Alzheimer'S Disease : JAD|January 15, 2018
Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on DementiaRaffaele Maletta, Nicoletta Smirne, Livia Bernardi, et al.
Pageof 20

Showing results (161-170 of 199) with videos related to

Sort By:
Pageof 20
Neurobiology of Aging|May 21, 2005
The effects of APOE and tau gene variability on risk of frontotemporal dementiaL Bernardi, R G Maletta, C Tomaino, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 8, 2011
Position paper of the Italian Society for the study of Dementias (SINDEM) on the proposal of a new lexicon on Alzheimer diseaseMassimo Musicco, Alessandro Padovani, Sandro Sorbi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 22, 2014
Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in ItalyB Borroni, R Turrone, D Galimberti, et al.
Neurogenetics|November 21, 2001
Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's diseaseM Nicolaou, Y Q Song, C A Sato, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 18, 2020
Early diagnosis of Alzheimer's disease: the role of biomarkers including advanced EEG signal analysis. Report from the IFCN-sponsored panel of expertsP M Rossini, R Di Iorio, F Vecchio, et al.
Frontiers in Aging Neuroscience|May 10, 2021
Being the Family Caregiver of a Patient With Dementia During the Coronavirus Disease 2019 LockdownMilena Zucca, Valeria Isella, Raffaele Di Lorenzo, et al.
Journal of Alzheimer'S Disease : JAD|March 23, 2011
A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological featuresMaura Gallo, Norina Marcello, Sabrina A M Curcio, et al.
Human Molecular Genetics|June 9, 2014
Hypermethylation of the CpG-island near the C9orf72 G₄C₂-repeat expansion in FTLD patientsZhengrui Xi, Innocenzo Rainero, Elisa Rubino, et al.
Neurology|May 8, 2015
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease familyMaria E Conidi, Livia Bernardi, Gianfranco Puccio, et al.
Journal of Alzheimer'S Disease : JAD|January 15, 2018
Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on DementiaRaffaele Maletta, Nicoletta Smirne, Livia Bernardi, et al.
Pageof 20