Theory of Mind and Its Neuropsychological and Quality of Life Correlates in the Early Stages of Amyotrophic Lateral Sclerosis by Trojsi, Francesca, Siciliano, Mattia, Russo, Antonio, Passaniti, Carla, Femiano, Cinzia, Ferrantino, Teresa, De Liguoro, Stefania, Lavorgna, Luigi, Monsurrò, Maria R, Tedeschi, Gioacchino, Santangelo, Gabriella

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Impact on children of a parent with ALS: a case-control study by Calvo, Vincenzo, Bianco, Francesca, Benelli, Enrico, Sambin, Marco, Monsurrò, Maria R, Femiano, Cinzia, Querin, Giorgia, Sorarù, Gianni, Palmieri, Arianna

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Dysfunctions within limbic–motor networks in amyotrophic lateral sclerosis by Passamonti, Luca, Fera, Francesco, Tessitore, Alessandro, Russo, Antonio, Cerasa, Antonio, Gioia, Cecilia M, Monsurrò, Maria R, Migliaccio, Raffaella, Tedeschi, Gioacchino, Quattrone, Aldo

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HFE p.H63D polymorphism does not influence ALS phenotype and survival by Chiò, Adriano, Mora, Gabriele, Sabatelli, Mario, Caponnetto, Claudia, Lunetta, Christian, Traynor, Bryan J, Johnson, Janel O, Nalls, Mike A, Calvo, Andrea, Moglia, Cristina, Borghero, Giuseppe, Monsurrò, Maria Rosaria, La Bella, Vincenzo, Volanti, Paolo, Simone, Isabella, Salvi, Fabrizio, Logullo, Francesco O, Nilo, Riva, Giannini, Fabio, Mandrioli, Jessica, Tanel, Raffaella, Murru, Maria Rita, Mandich, Paola, Zollino, Marcella, Conforti, Francesca L, Penco, Silvana, Brunetti, Maura, Barberis, Marco, Restagno, Gabriella

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Establishment and characterization of a human neuroectodermal cell line (TB) from a cerebrospinal fluid specimen by Sorrentino, Giuseppe, Monsurrò, Maria R, Pettinato, Guido, Vanni, Roberta, Zuddas, Alessandro, Di Porzio, Umberto, Bonavita, Vincenzo

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A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD by Renton, Alan E., Majounie, Elisa, Waite, Adrian, Simón-Sánchez, Javier, Rollinson, Sara, Gibbs, J. Raphael, Schymick, Jennifer C., Laaksovirta, Hannu, van Swieten, John C., Myllykangas, Liisa, Kalimo, Hannu, Paetau, Anders, Abramzon, Yevgeniya, Remes, Anne M., Kaganovich, Alice, Scholz, Sonja W., Duckworth, Jamie, Ding, Jinhui, Harmer, Daniel W., Hernandez, Dena G., Johnson, Janel O., Mok, Kin, Ryten, Mina, Trabzuni, Danyah, Guerreiro, Rita J., Orrell, Richard W., Neal, James, Murray, Alex, Pearson, Justin, Jansen, Iris E., Sondervan, David, Seelaar, Harro, Blake, Derek, Young, Kate, Halliwell, Nicola, Callister, Janis Bennion, Toulson, Greg, Richardson, Anna, Gerhard, Alex, Snowden, Julie, Mann, David, Neary, David, Nalls, Michael A., Peuralinna, Terhi, Jansson, Lilja, Isoviita, Veli-Matti, Kaivorinne, Anna-Lotta, Hölttä-Vuori, Maarit, Ikonen, Elina, Sulkava, Raimo, Benatar, Michael, Wuu, Joanne, Chiò, Adriano, Restagno, Gabriella, Borghero, Giuseppe, Sabatelli, Mario, Heckerman, David, Rogaeva, Ekaterina, Zinman, Lorne, Rothstein, Jeffrey D., Sendtner, Michael, Drepper, Carsten, Eichler, Evan E., Alkan, Can, Abdullaev, Ziedulla, Pack, Svetlana D., Dutra, Amalia, Pak, Evgenia, Hardy, John, Singleton, Andrew, Williams, Nigel M., Heutink, Peter, Pickering-Brown, Stuart, Morris, Huw R., Tienari, Pentti J., Traynor, Bryan J.

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A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis by Fogh, Isabella, Ratti, Antonia, Gellera, Cinzia, Lin, Kuang, Tiloca, Cinzia, Moskvina, Valentina, Corrado, Lucia, Sorarù, Gianni, Cereda, Cristina, Corti, Stefania, Gentilini, Davide, Calini, Daniela, Castellotti, Barbara, Mazzini, Letizia, Querin, Giorgia, Gagliardi, Stella, Del Bo, Roberto, Conforti, Francesca L, Siciliano, Gabriele, Inghilleri, Maurizio, Saccà, Francesco, Bongioanni, Paolo, Penco, Silvana, Corbo, Massimo, Sorbi, Sandro, Filosto, Massimiliano, Ferlini, Alessandra, Di Blasio, Anna M, Signorini, Stefano, Shatunov, Aleksey, Jones, Ashley, Shaw, Pamela J, Morrison, Karen E, Farmer, Anne E, Van Damme, Philip, Robberecht, Wim, Chiò, Adriano, Traynor, Bryan J, Sendtner, Michael, Melki, Judith, Meininger, Vincent, Hardiman, Orla, Andersen, Peter M, Leigh, Nigel P, Glass, Jonathan D, Overste, Daniel, Diekstra, Frank P, Veldink, Jan H, van Es, Michael A, Shaw, Christopher E, Weale, Michael E, Lewis, Cathryn M, Williams, Julie, Brown, Robert H, Landers, John E, Ticozzi, Nicola, Ceroni, Mauro, Pegoraro, Elena, Comi, Giacomo P, D'Alfonso, Sandra, van den Berg, Leonard H, Taroni, Franco, Al-Chalabi, Ammar, Powell, John, Silani, Vincenzo

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Small extracellular vesicles deliver miR-21 and miR-217 as pro-senescence effectors to endothelial cells by Mensà, Emanuela, Guescini, Michele, Giuliani, Angelica, Bacalini, Maria Giulia, Ramini, Deborah, Corleone, Giacomo, Ferracin, Manuela, Fulgenzi, Gianluca, Graciotti, Laura, Prattichizzo, Francesco, Sorci, Leonardo, Battistelli, Michela, Monsurrò, Vladia, Bonfigli, Anna Rita, Cardelli, Maurizio, Recchioni, Rina, Marcheselli, Fiorella, Latini, Silvia, Maggio, Serena, Fanelli, Mirco, Amatori, Stefano, Storci, Gianluca, Ceriello, Antonio, Stocchi, Vilberto, De Luca, Maria, Magnani, Luca, Rippo, Maria Rita, Procopio, Antonio Domenico, Sala, Claudia, Budimir, Iva, Bassi, Cristian, Negrini, Massimo, Garagnani, Paolo, Franceschi, Claudio, Sabbatinelli, Jacopo, Bonafè, Massimiliano, Olivieri, Fabiola

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Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? by Mancuso, Michelangelo, Conforti, Francesca Luisa, Rocchi, Anna, Tessitore, Alessandro, Muglia, Maria, Tedeschi, Gioacchino, Panza, Daniela, Monsurrò, MariaRosaria, Sola, Patrizia, Mandrioli, Jessica, Choub, Anna, DelCorona, Alberto, Manca, Maria Laura, Mazzei, Rosalucia, Sprovieri, Teresa, Filosto, Massimiliano, Salviati, Alessandro, Valentino, Paola, Bono, Francesco, Caracciolo, Manuela, Simone, Isabella Laura, La Bella, Vincenzo, Majorana, Giovanni, Siciliano, Gabriele, Murri, Luigi, Quattrone, Aldo

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A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and mental retardation in a family with tuberous sclerosis by Argenziano, Giuseppe, Monsurrò, Maria Rosaria, Pazienza, Raniero, Delfino, Mario

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