Lattante, Serena
Dettaglio
Lattante, Serena
ROMA - Dipartimento di Scienze della vita e sanità pubblica
Pubblicazioni
Risultati 1 - 20 di 69 (tempo di esecuzione: 0.037 secondi).
Data di pubblicazione | Titolo | Autore(i) | File | |
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1 | 2013 | A novel compound heterozygous ALS2 mutation in two Italian siblings with juvenile amyotrophic lateral sclerosis | Luigetti, Marco; Lattante, Serena; Conte, Amelia; Romano, Angela; Zollino, Marcella; Marangi, Giuseppe; Sabatelli, Mario | - |
2 | 2011 | A novel L67P SOD1 mutation in an Italian ALS patient. | Del Grande, Alessandra; Luigetti, Marco; Conte, Amelia; Mancuso, Irene; Lattante, Serena; Marangi, Giuseppe; Zollino, Marcella; Sabatelli, Mario; Stipa, G. | - |
3 | 2020 | Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome | Amenta, S.; Frangella, S.; Marangi, G.; Lattante, S.; Ricciardi, S.; Doronzio, P. N.; Orteschi, D.; Veredice, C.; Contaldo, I.; Zampino, G.; Gentile, M.; Scarano, E.; Graziano, C.; Zollino, M. | - |
4 | 2020 | ALS skin fibroblasts reveal oxidative stress and ERK1/2-mediated cytoplasmic localization of TDP-43 | Romano, Nicla; Catalani, Alessia; Lattante, Serena; Belardo, Antonio; Proietti, Silvia; Bertini, Laura; Silvestri, Federica; Catalani, Elisabetta; Cervia, Davide; Zolla, Lello; Sabatelli, Mario; Welshhans, Kristy; Ceci, Marcello | - |
5 | 2015 | ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion | Chiò, A; Mora, G; Sabatelli, Mario; Caponnetto, C; Lunetta, C; Traynor, Bj; Johnson, Jo; Nalls, Ma; Calvo, A; Moglia, C; Borghero, G; Trojsi, F; La Bella, V; Volanti, P; Simone, I; Salvi, F; Logullo, Fo; Riva, N; Carrera, P; Giannini, F; Mandrioli, J; Tanel, R; Capasso, M; Tremolizzo, L; Battistini, S; Murru, Mr; Origone, P; Zollino, Marcella; Penco, S; Mazzini, L; D'Alfonso, S; Restagno, G; Brunetti, M; Barberis, M; Conforti, Fl; Conte, Amelia; Luigetti, Marco; Lattante, Serena; Marangi, Giuseppe | - |
6 | 2018 | ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis | Lattante, Serena; Pomponi, Maria Grazia; Conte, Amelia; Marangi, Giuseppe; Bisogni, Giulia; Patanella, Agata Katia; Meleo, Emiliana; Lunetta, Christian; Riva, Nilo; Mosca, Lorena; Carrera, Paola; Bee, Marco; Zollino, Marcella; Sabatelli, Mario | - |
7 | 2015 | ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry | Borghero, G; Pugliatti, M; Marrosu, F; Marrosu, Mg; Murru, Mr; Floris, G; Cannas, A; Parish, Ld; Cau, Tb; Loi, D; Ticca, A; Traccis, S; Manera, U; Canosa, A; Moglia, C; Calvo, A; Barberis, M; Brunetti, M; Renton, Ae; Nalls, Ma; Traynor, Bj; Restagno, G; Chiò, A; Sabatelli, Mario; Zollino, Marcella; Conte, Amelia; Luigetti, Marco; Lattante, Serena; Marangi, Giuseppe | - |
8 | 2015 | ATXN2 polyQ intermediate repeats are a modifier of ALS survival | Chiò, A; Calvo, A; Moglia, C; Canosa, A; Brunetti, M; Barberis, M; Restagno, G; Conte, Amelia; Bisogni, Giulia; Marangi, Giuseppe; Moncada, Alice; Lattante, Serena; Zollino, Marcella; Sabatelli, Mario; Bagarotti, A; Corrado, L; Mora, G; Bersano, E; Mazzini, L; D'Alfonso, S. | - |
9 | 2017 | ATXN2 trinucleotide repeat length correlates with risk of ALS | Sproviero, William; Shatunov, Aleksey; Stahl, Daniel; Shoai, Maryam; van Rheenen, Wouter; Jones, Ashley R; Al Sarraj, Safa; Andersen, Peter M; Bonini, Nancy M; Conforti, Francesca L; Van Damme, Philip; Daoud, Hussein; Del Mar Amador, Maria; Fogh, Isabella; Forzan, Monica; Gaastra, Ben; Gellera, Cinzia; Gitler, Aaron D; Hardy, John; Fratta, Pietro; La Bella, Vincenzo; Le Ber, Isabelle; Van Langenhove, Tim; Lattante, Serena; Lee, Yi Chung; Malaspina, Andrea; Meininger, Vincent; Millecamps, Stéphanie; Orrell, Richard; Rademakers, Rosa; Robberecht, Wim; Rouleau, Guy; Ross, Owen A; Salachas, Francois; Sidle, Katie; Smith, Bradley N; Soong, Bing Wen; Sorarù, Gianni; Stevanin, Giovanni; Kabashi, Edor; Troakes, Claire; van Broeckhoven, Christine; Veldink, Jan H; van den Berg, Leonard H; Shaw, Christopher E; Powell, John F; Al Chalabi, Ammar | Open Access |
10 | 2015 | CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients | Chiò, A; Mora, G; Sabatelli, Mario; Caponnetto, C; Traynor, Bj; Johnson, Jo; Nalls, Ma; Calvo, A; Moglia, C; Borghero, G; Monsurrò, Mr; La Bella, V; Volanti, P; Simone, I; Salvi, F; Logullo, Fo; Nilo, R; Battistini, S; Mandrioli, J; Tanel, R; Murru, Mr; Mandich, P; Zollino, Marcella; Conforti, Fl; Brunetti, M; Barberis, M; Restagno, G; Penco, S; Lunetta, C; Conte, Amelia; Luigetti, Marco; Lattante, Serena; Marangi, Giuseppe | - |
11 | 2012 | Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation | Conte, Andrea; Lattante, Serena; Luigetti, Marco; Del Grande, Alessandra; Romano, A; Marcaccio, A; Marangi, Giuseppe; Rossini, Paolo Maria; Neri, Giovanni; Zollino, Marcella; Sabatelli, Mario | - |
12 | 2012 | Classification of familial amyotrophic lateral sclerosis by family history: effects on frequency of genes mutation | Conte, Amelia; Lattante, Serena; Luigetti, Marco; Del Grande, Alessandra; Romano, Antonino; Marcaccio, A; Marangi, Giuseppe; Rossini, Paolo Maria; Neri, Geraldina; Zollino, Marcella; Sabatelli, Mario | - |
13 | 2019 | Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS | Lattante, Serena; Doronzio, Paolo Niccolo'; Marangi, Giuseppe; Conte, Amelia; Bisogni, Giulia; Bernardo, Daniela; Russo, Tommaso; Lamberti, Dante; Patrizi, Sara; Paolo Apollo, Francesco; Lunetta, Christian; Scarlino, Stefania; Pozzi, Laura; Zollino, Marcella; Riva, Nilo; Sabatelli, Mario | - |
14 | 2014 | Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders | Lattante, Serena; Millecamps, S; Stevanin, G; Rivaud Péchoux, S; Moigneu, C; Camuzat, A; Da Barroca, S; Mundwiller, E; Couarch, P; Salachas, F; Hannequin, D; Meininger, V; Pasquier, F; Seilhean, D; Couratier, P; Danel Brunaud, V; Bonnet, A; Tranchant, C; Leguern, E; Brice, A; Le Ber, I; Kabashi, E. | - |
15 | 2012 | Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease | Lattante, Serena; Conte, Amelia; Zollino, Marcella; Luigetti, Marco; Del Grande, Alessandra; Marangi, Giuseppe; Romano, Alberto; Marcaccio, A; Meleo, Emiliana; Bisogni, Giulia; Rossini, Paolo Maria; Sabatelli, Mario | - |
16 | 2011 | D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation | Del Grande, Alessandra; Conte, Amelia; Lattante, Serena; Luigetti, Marco; Marangi, Giuseppe; Zollino, Marcella; Madia, Francesca; Bisogni, Giulia; Sabatelli, Mario | - |
17 | 2014 | Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions | Lattante, Serena; Le Ber, I; Galimberti, D; Serpente, M; Rivaud Péchoux, S; Camuzat, A; Clot, F; Fenoglio, C; Scarpini, E; Brice, A; Kabashi, E. | - |
18 | 2015 | Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD) | Lattante, Serena; Ciura, S; Rouleau, Ga; Kabashi, E. | - |
19 | 2016 | Defining the spectrum of frontotemporal dementias associated with TARDBP mutations. | Caroppo, P; Camuzat, A; Guillot Noel, L; Thomas Antérion, C; Couratier, P; Wong, Th; Teichmann, M; Golfier, V; Auriacombe, S; Belliard, S; Laurent, B; Lattante, Serena; Millecamps, S; Clot, F; Dubois, B; Van Swieten, Jc; Brice, A; Le Ber, I. | - |
20 | 2012 | Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients | Lattante, Serena; Marangi, Giuseppe; Luigetti, Marco; Conte, Amelia; Mandrioli, J; Del Grande, Alessandra; Zollino, Marcella; Sabatelli, Mario | - |