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Neurobiology of Aging
|
May 21, 2005
The effects of APOE and tau gene variability on risk of frontotemporal dementia
L 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 disease
Massimo 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 Italy
B 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 disease
M 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 experts
P 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 Lockdown
Milena 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 features
Maura 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 patients
Zhengrui Xi, Innocenzo Rainero, Elisa Rubino, et al.
Neurology
|
May 8, 2015
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family
Maria 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 Dementia
Raffaele Maletta, Nicoletta Smirne, Livia Bernardi, et al.
Page
of 20
Search research articles
Search
Showing results (161-170 of 199) with videos related to
Sort By:
Page
of 20
Neurobiology of Aging
|
May 21, 2005
The effects of APOE and tau gene variability on risk of frontotemporal dementia
L 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 disease
Massimo 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 Italy
B 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 disease
M 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 experts
P 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 Lockdown
Milena 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 features
Maura 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 patients
Zhengrui Xi, Innocenzo Rainero, Elisa Rubino, et al.
Neurology
|
May 8, 2015
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family
Maria 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 Dementia
Raffaele Maletta, Nicoletta Smirne, Livia Bernardi, et al.
Page
of 20