Lattante, Serena

Lattante, Serena  

ROMA - Dipartimento di Scienze della vita e sanità pubblica  

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Data di pubblicazione Titolo Autore(i) File
1-gen-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
1-gen-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.
1-gen-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.
1-gen-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
1-gen-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
1-gen-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
1-gen-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
1-gen-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.
1-gen-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
1-gen-2022 Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients Perciballi, E.; Bovio, F.; Rosati, J.; Arrigoni, F.; D'anzi, A.; Lattante, S.; Gelati, M.; De Marchi, F.; Lombardi, I.; Ruotolo, G.; Forcella, M.; Mazzini, L.; D'alfonso, S.; Corrado, L.; Sabatelli, M.; Conte, A.; De Gioia, L.; Martino, S.; Vescovi, A. L.; Fusi, P.; Ferrari, D.
1-gen-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
1-gen-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
1-gen-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
1-gen-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
1-gen-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.
1-gen-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
1-gen-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
1-gen-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.
1-gen-2015 Defining the genetic connection linking amyotrophic lateral sclerosis (ALS) with frontotemporal dementia (FTD) Lattante, Serena; Ciura, S; Rouleau, Ga; Kabashi, E.
1-gen-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.