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Journal of Alzheimer'S Disease : JAD|August 22, 2013
Identification of three novel LRRK2 mutations associated with Parkinson's disease in a Calabrian populationMaria Anfossi, Rosanna Colao, Maura Gallo, et al.Neurobiology of Aging|February 8, 2011
Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementiaMaria Anfossi, Romina Vuono, Raffaele Maletta, 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.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|October 30, 2016
Role of Niemann-Pick Type C Disease Mutations in DementiaChiara Cupidi, Francesca Frangipane, Maura Gallo, 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.Journal of Alzheimer'S Disease : JAD|February 23, 2016
Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus ProtocolMartina Bocchetta, Anna Mega, Livia Bernardi, et al.Neurobiology of Aging|May 24, 2017
The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease familyMaura Gallo, Francesca Frangipane, Chiara Cupidi, et al.Journal of Alzheimer'S Disease : JAD|January 28, 2017
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal DementiaRaffaele Ferrari, Mario Grassi, Francesca Graziano, et al.Neurobiology of Aging|July 24, 2012
Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern ItalyLivia Bernardi, Francesca Frangipane, Nicoletta Smirne, et al.Pageof 6