Showing results (61-70 of 74) with videos related to
Sort By:
Pageof 8
Neurobiology of Aging|October 22, 2018
ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementiaElisa Rubino, Cecilia Mancini, Silvia Boschi, et al.Journal of Hypertension|December 2, 2010
Hypertension and migraine comorbidity: prevalence and risk of cerebrovascular events: evidence from a large, multicenter, cross-sectional survey in Italy (MIRACLES study)Giuseppe Mancia, Enrico Agabiti Rosei, Ettore Ambrosioni, et al.Dementia and Geriatric Cognitive Disorders|September 30, 2009
Absence of TARDBP gene mutations in an italian series of patients with frontotemporal lobar degenerationSalvatore Gallone, Maria Teresa Giordana, Elio Scarpini, et al.Neurology|September 14, 2012
SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosisElisa Rubino, Innocenzo Rainero, Adriano Chiò, et al.The Journal of Headache and Pain|May 15, 2012
Italian guidelines for primary headaches: 2012 revised versionPaola Sarchielli, Franco Granella, Maria Pia Prudenzano, 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.BMC Medical Genetics|May 1, 2015
An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2Cecilia Mancini, Laura Orsi, Yiran Guo, et al.Journal of Alzheimer'S Disease : JAD|January 13, 2016
PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian PopulationEmanuela Oldoni, Giorgio G Fumagalli, Maria Serpente, et al.Acta Neuropathologica|February 27, 2015
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patientsZhengrui Xi, Ming Zhang, Amalia C Bruni, 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.Pageof 8