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Archives of Neurology|October 22, 2003
A case of dementia parkinsonism resembling progressive supranuclear palsy due to mutation in the tau protein genePaola Soliveri, Giacomina Rossi, Daniela Monza, et al.Journal of Alzheimer'S Disease : JAD|October 11, 2012
Mutations in MAPT gene cause chromosome instability and introduce copy number variations widely in the genomeGiacomina Rossi, Donatella Conconi, Elena Panzeri, et al.Journal of Alzheimer'S Disease : JAD|March 12, 2009
A novel Italian presenilin 2 gene mutation with prevalent behavioral phenotypeGabriella Marcon, Giuseppe Di Fede, Giorgio Giaccone, et al.Journal of Alzheimer'S Disease : JAD|March 27, 2018
Frontotemporal Dementia and Chorea Associated with a Compound Heterozygous TREM2 MutationVeronica Redaelli, Ettore Salsano, Lara Colleoni, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 2008
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndromeGiacomina Rossi, Cecilia Marelli, Laura Farina, et al.European Journal of Neurology|January 12, 2022
MAPT Q336H mutation: Intrafamilial phenotypic heterogeneity in a new Italian familyCristina Villa, Giacomina Rossi, Ilaria Bizzozero, et al.Neurobiology of Disease|October 11, 2022
GRN-/- iPSC-derived cortical neurons recapitulate the pathological findings of both frontotemporal lobar degeneration and neuronal ceroidolipofuscinosisPatrizia Bossolasco, Sara Cimini, Emanuela Maderna, et al.International Journal of Molecular Sciences|November 26, 2022
Pathological 25 kDa C-Terminal Fragments of TDP-43 Are Present in Lymphoblastoid Cell Lines and Extracellular Vesicles from Patients Affected by Frontotemporal Lobar Degeneration and Neuronal Ceroidolipofuscinosis Carrying a <i>GRN</i> MutationSara Cimini, Sonia Bellini, Claudia Saraceno, et al.Neurogenetics|November 13, 2013
Mutations in MAPT give rise to aneuploidy in animal models of tauopathyGiacomina Rossi, Donatella Conconi, Elena Panzeri, et al.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.Pageof 9