Neural correlates of altered insight in frontotemporal dementia: a systematic review von Muñoz-Neira, Carlos, Tedde, Andrea, Coulthard, Elizabeth, Thai, N. Jade, Pennington, Catherine

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Tomm40 polymorphisms in Italian Alzheimer’s disease and frontotemporal dementia patients von Bagnoli, Silvia, Piaceri, Irene, Tedde, Andrea, Bessi, Valentina, Bracco, Laura, Sorbi, Sandro, Nacmias, Benedetta

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Interleukin-10 promoter polymorphisms influence susceptibility to ulcerative colitis in a gender-specific manner von Tedde, Andrea, Laura Putignano, Anna, Bagnoli, Siro, Congregati, Caterina, Milla, Monica, Sorbi, Sandro, Genuardi, Maurizio, Papi, Laura

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Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer’s disease von Nacmias, Benedetta, Piccini, Carolina, Bagnoli, Silvia, Tedde, Andrea, Cellini, Elena, Bracco, Laura, Sorbi, Sandro

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Association Study of Genetic Variants in CDKN2A/CDKN2B Genes/Loci with Late-Onset Alzheimer's Disease von Tedde, Andrea, Piaceri, Irene, Bagnoli, Silvia, Lucenteforte, Ersilia, Ueberham, Uwe, Arendt, Thomas, Sorbi, Sandro, Nacmias, Benedetta

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Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer’s disease von Tedde, Andrea, Bartoli, Antonella, Piaceri, Irene, Ferrara, Sara, Bagnoli, Silvia, Serio, Antonio, Sorbi, Sandro, Nacmias, Benedetta

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Clinical presentation and prognosis of COVID-19 in older adults with hypothyroidism: data from the GeroCovid observational study von Bagalà, V., Sala, A., Trevisan, C., Okoye, C., Incalzi, R. A., Monzani, F., Volpato, S.

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Mutation analysis of patients with neurodegenerative disorders using NeuroX array von Ghani, Mahdi, Lang, Anthony E, Zinman, Lorne, Nacmias, Benedetta, Sorbi, Sandro, Bessi, Valentina, Tedde, Andrea, Tartaglia, Maria Carmela, Surace, Ezequiel I, Sato, Christine, Moreno, Danielle, Xi, Zhengrui, Hung, Rachel, Nalls, Mike A, Singleton, Andrew, St George-Hyslop, Peter, Rogaeva, Ekaterina

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The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family von Gallo, Maura, Frangipane, Francesca, Cupidi, Chiara, De Bartolo, Matteo, Turone, Sabina, Ferrari, Camilla, Nacmias, Benedetta, Grimaldi, Giuliana, Laganà, Valentina, Colao, Rosanna, Bernardi, Livia, Anfossi, Maria, Conidi, Maria Elena, Vasso, Franca, Curcio, Sabrina Anna Maria, Mirabelli, Maria, Smirne, Nicoletta, Torchia, Giusi, Muraca, Maria Gabriella, Puccio, Gianfranco, Di Lorenzo, Raffaele, Piccininni, Maristella, Tedde, Andrea, Maletta, Raffaele Giovanni, Sorbi, Sandro, Bruni, Amalia Cecilia

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Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians von Piaceri, Irene, Bagnoli, Silvia, Tedde, Andrea, Sorbi, Sandro, Nacmias, Benedetta

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KIBRA gene variants are associated with episodic memory performance in subjective memory complaints von Nacmias, Benedetta, Bessi, Valentina, Bagnoli, Silvia, Tedde, Andrea, Cellini, Elena, Piccini, Carolina, Sorbi, Sandro, Bracco, Laura

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Imaging and Cognitive Reserve Studies Predict Dementia in Presymptomatic Alzheimer's Disease Subjects von Ferrari, Camilla, Nacmias, Benedetta, Bagnoli, Silvia, Piaceri, Irene, Lombardi, Gemma, Pradella, Silvia, Tedde, Andrea, Sorbi, Sandro

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Semantic dementia associated with mutation V363I in the tau gene von Bessi, Valentina, Bagnoli, Silvia, Nacmias, Benedetta, Tedde, Andrea, Sorbi, Sandro, Bracco, Laura

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Analyses of the role of the glucocorticoid receptor gene polymorphism (rs41423247) as a potential moderator in the association between childhood overweight, psychopathology, and cl... von Castellini, Giovanni, Lelli, Lorenzo, Tedde, Andrea, Piaceri, Irene, Bagnoli, Silvia, Lucenteforte, Ersilia, Sorbi, Sandro, Monteleone, Alessio Maria, Hudziak, James J, Nacmias, Benedetta, Ricca, Valdo

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Suitability of neuropsychological tests in patients with vascular dementia (VaD) von Bagnoli, Silvia, Failli, Ylenia, Piaceri, Irene, Rinnoci, Valentina, Bessi, Valentina, Tedde, Andrea, Nacmias, Benedetta, Sorbi, Sandro

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A case of atypical early-onset Alzheimer’s disease carrying the missense mutation Thr354Ile in exon 10 of the PSEN1 gene von Marini, Sandro, Lucidi, Giulia, Tedde, Andrea, Bessi, Valentina, Nacmias, Benedetta

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Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas von DE VITIS, L. R, TEDDE, A, VITELLI, F, AMMANNATI, F, MENNONNA, P, BIGOZZI, U, MONTALI, E, PAPI, L

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The novel PSEN1 M84V mutation associated to frontal disexecutive syndrome, spastic paraparesis and cerebellar atrophy in a dominant Alzheimer’s disease family von Gallo, Maura, Frangipane, Francesca, Cupidi, Chiara, De Bartolo, Matteo, Turone, Sabina, Ferrari, Camilla, Nacmias, Benedetta, Grimaldi, Giuliana, Laganà, Valentina, Colao, Rosanna, Bernardi, Livia, Anfossi, Maria, Conidi, Maria Elena, Vasso, Franca, Curcio, Sabrina Anna Maria, Mirabelli, Maria, Smirne, Nicoletta, Torchia, Giusi, Muraca, Maria Gabriella, Puccio, Gianfranco, Di Lorenzo, Raffaele, Piccininni, Maristella, Tedde, Andrea, Maletta, Raffaele Giovanni, Sorbi, Sandro, Bruni, Amalia Cecilia

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Progranulin Genetic Screening in Frontotemporal Lobar Degeneration Patients From Central Italy von Bagnoli, Silvia, Piaceri, Irene, Tedde, Andrea, Piacentini, Silvia, Nannucci, Serena, Bracco, Laura, Sorbi, Sandro, Nacmias, Benedetta

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Association of IL10 promoter polymorphism in Italian Alzheimer's disease von Bagnoli, Silvia, Cellini, Elena, Tedde, Andrea, Nacmias, Benedetta, Piacentini, Silvia, Bessi, Valentina, Bracco, Laura, Sorbi, Sandro

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