1. C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts. (15th December 2020) Authors: Costa, Beatrice; Manzoni, Claudia; Bernal-Quiros, Manuel; Kia, Demis A.; Aguilar, Miquel; Alvarez, Ignacio; Alvarez, Victoria; Andreassen, Ole; Anfossi, Maria; Bagnoli, Silvia; Benussi, Luisa; Bernardi, Livia; Binetti, Giuliano; Blackburn, Daniel; Boada, Mercè; Borroni, Barbara; Bowns, Lucy; Bråt... Journal: Neurology Issue: Volume 95:Number 24(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Evolution of genetic testing supports precision medicine for caring Alzheimer's disease patients. (October 2021) Authors: Bruni, Amalia Cecilia; Bernardi, Livia; Maletta, Raffaele Journal: Current opinion in pharmacology Issue: Volume 60(2021) Page Start: 275 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. IP6K3 and IPMK variations in LOAD and longevity: Evidence for a multifaceted signaling network at the crossroad between neurodegeneration and survival. (April 2021) Authors: Dato, Serena; Crocco, Paolina; De Rango, Francesco; Iannone, Francesca; Maletta, Raffaele; Bruni, Amalia C.; Saiardi, Adolfo; Rose, Giuseppina; Passarino, Giuseppe Journal: Mechanisms of ageing and development Issue: Volume 195(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. NGF controls APP cleavage by downregulating APP phosphorylation at Thr668: relevance for Alzheimer's disease. Issue 4 (13th April 2016) Authors: Triaca, Viviana; Sposato, Valentina; Bolasco, Giulia; Ciotti, Maria Teresa; Pelicci, Piergiuseppe; Bruni, Amalia C.; Cupidi, Chiara; Maletta, Raffaele; Feligioni, Marco; Nisticò, Robert; Canu, Nadia; Calissano, Pietro Journal: Aging cell Issue: Volume 15:Issue 4(2016) Page Start: 661 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. Issue 6 (June 2018) Authors: Pottier, Cyril; Zhou, Xiaolai; Perkerson, Ralph B; Baker, Matt; Jenkins, Gregory D; Serie, Daniel J; Ghidoni, Roberta; Benussi, Luisa; Binetti, Giuliano; López de Munain, Adolfo; Zulaica, Miren; Moreno, Fermin; Le Ber, Isabelle; Pasquier, Florence; Hannequin, Didier; Sánchez-Valle, Raquel; Antone... Journal: Lancet neurology Issue: Volume 17:Issue 6(2018) Page Start: 548 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Prevalence of heterozygous mutations in Niemann-Pick type C genes in a cohort of progressive supranuclear palsy. (October 2020) Authors: Picillo, Marina; Amboni, Marianna; Bruni, Amalia; Maletta, Raffaele; Barone, Paolo Journal: Parkinsonism & related disorders Issue: Volume 79(2020) Page Start: 9 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗