Search Results - Lauria, P. B.

Refine Results
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10
  11. 11

    Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways by Cirulli, Elizabeth T., Lasseigne, Brittany N., Petrovski, Slavé, Sapp, Peter C., Dion, Patrick A., Leblond, Claire S., Couthouis, Julien, Lu, Yi-Fan, Wang, Quanli, Krueger, Brian J., Ren, Zhong, Keebler, Jonathan, Han, Yujun, Levy, Shawn E., Boone, Braden E., Wimbish, Jack R., Waite, Lindsay L., Jones, Angela L., Carulli, John P., Day-Williams, Aaron G., Staropoli, John F., Xin, Winnie W., Chesi, Alessandra, Raphael, Alya R., McKenna-Yasek, Diane, Cady, Janet, de Jong, J. M. B. Vianney, Kenna, Kevin P., Smith, Bradley N., Topp, Simon, Miller, Jack, Gkazi, Athina, Al-Chalabi, Ammar, van den Berg, Leonard H., Veldink, Jan, Silani, Vincenzo, Ticozzi, Nicola, Shaw, Christopher E., Baloh, Robert H., Appel, Stanley, Simpson, Ericka, Lagier-Tourenne, Clotilde, Pulst, Stefan M., Gibson, Summer, Trojanowski, John Q., Elman, Lauren, McCluskey, Leo, Grossman, Murray, Shneider, Neil A., Chung, Wendy K., Ravits, John M., Glass, Jonathan D., Sims, Katherine B., Van Deerlin, Vivianna M., Maniatis, Tom, Hayes, Sebastian D., Ordureau, Alban, Swarup, Sharan, Landers, John, Baas, Frank, Allen, Andrew S., Bedlack, Richard S., Harper, J. Wade, Gitler, Aaron D., Rouleau, Guy A., Brown, Robert, Harms, Matthew B., Cooper, Gregory M., Harris, Tim, Myers, Richard M., Goldstein, David B.

    Get full text
    Article
  12. 12
  13. 13
  14. 14
  15. 15
  16. 16

    Genome-wide Analyses Identify KIF5A as a Novel ALS Gene by Kenna, Kevin P., Chia, Ruth, Dominov, Janice A., Nalls, Mike A., van Vugt, Joke J.F.A., Simone, Isabella, Caredda, Carla, Milia, Antonio, Floris, Gianluca, Caponnetto, Claudia, Mandich, Paola, Mora, Gabriele, Sideri, Riccardo, Penco, Silvana, Mandrioli, Jessica, Trojsi, Francesca, Ticca, Anna, Ortu, Enzo, Pugliatti, Maura, Benigni, Michele, Brunetti, Maura, Marrali, Giuseppe, Riva, Nilo, Conforti, Francesca L., Messina, Sonia, D’Alfonso, Sandra, Baloh, Robert H., Penny, Michelle, Moreno, Cristiane de Araujo Martins, Chung, Wendy K., Cirulli, Elizabeth T., Harris, Tim, Krueger, Brian J., Lasseigne, Brittany N., McKenna-Yasek, Diane, Myers, Richard M., Pulst, Stefan M., Raphael, Alya R., Rouleau, Guy A., Sapp, Peter C., Waite, Lindsay L., Wang, Quanli, Ostrow, Lyle W., Baas, Frank, Zaitlen, Noah, Hornstein, Eran, Patsopoulos, Nikolaos A., Kaye, Julia, Wyman, Stacia, LeNail, Alexander, Baxi, Emily, LeNail, Alex, Benatar, Michael, Hussain, Sumaira, Swenson, Andrea, Jackson, Carlayne, So, Yuen, Wuu, Joanne, Silani, Vincenzo, Fogh, Isabella, Cereda, Cristina, Ceroni, Mauro, Mazzini, Letizia, Maderna, Luca, Sorarù, Gianni, Bernard, Emilien, Laaksovirta, Hannu, McKenna-Yasek, Diane, Asress, Seneshaw, Al-Sarraj, Safa, Scholz, Sonja W., MacGowan, Daniel J.L., Kirby, Janine, Pioro, Erik P., Pamphlett, Roger, Dunckley, Travis L., Troncoso, Juan C., Moisse, Matthieu, Drory, Vivian E., Turner, Martin R., Blair, Ian P., de Carvalho, Mamede, Hide, Winston, Glass, Jonathan, Mill, Jonathan, Newhouse, Stephen, Pulit, Sara, Robberecht, Wim, Shaw, Pamela, van den Berg, Leonard, Williams, Kelly L., Zatz, Mayana, Rothstein, Jeffrey D., Simmons, Zachary, Van Damme, Philip, Sabatelli, Mario, Trojanowski, John Q., Brown, Robert H., Veldink, Jan H., Tienari, Pentti

    Get full text
    Article
  17. 17

    Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores by de Rojas, Itziar, Tesi, Niccolo, Zettergren, Anna, Montrreal, Laura, Antonell, Anna, Bis, Joshua C., González-Perez, Antonio, Calero, Miguel, Blesa, Rafael, Sotolongo-Grau, Oscar, Benaque, Alba, Benussi, Alberto, de Mendonça, Alexandre, Arias Pastor, Alfonso, Espinosa, Ana, Sanabria, Ángela, DeStefano, Anita L., Schneider, Anja, Haapasalo, Annakaisa, Tybjærg-Hansen, Anne, Hartmann, Annette M., Spottke, Annika, Corbatón-Anchuelo, Arturo, Arosio, Beatrice, Nacmias, Benedetta, Kunkle, Brian W., Charbonnier, Camille, Martínez Rodríguez, Carmen, Reynolds, Chandra A., Fenoglio, Chiara, Van Broeckhoven, Christine, Clark, Christopher, Buiza-Rueda, Dolores, Alcolea, Daniel, Grünblatt, Edna, Dardiotis, Efthimios, Conti, Elisa, Boerwinkle, Eric, Ferri, Evelyn, Pasquier, Florence, Mangialasche, Francesca, Hadjigeorgiou, Georgios, Spalletta, Gianfranco, Soininen, Hilkka, Rainero, Innocenzo, Hort, Jakub, Kornhuber, Johannes, Pineda, Juan A., Fortea, Juan, Popp, Julius, Buerger, Katharina, Molina-Porcel, Laura, Wang, Li-San, Farotti, Lucia, Tsolaki, Magda, Rosende-Roca, Maitée, Hulsman, Marc, Spallazzi, Marco, Bernal Sánchez-Arjona, María, Dalmasso, Maria Carolina, Fernández-Fuertes, Marta, Herrmann, Martin J., Vyhnalek, Martin, Yannakoulia, Mary, Schmid, Matthias, Armstrong, Nicola J., Skrobot, Olivia Anna, Quenez, Olivier, Bossù, Paola, Caffarra, Paolo, Dionigi Rossi, Paolo, Sakka, Paraskevi, Riederer, Peter, Kalaria, Rajesh N., Mayeux, Richard, Vandenberghe, Rik, Sorbi, Sandro, Hägg, Sara, Engelborghs, Sebastiaan, Helisalmi, Seppo, Kern, Silke, Boschi, Silvia, Fostinelli, Silvia, Gil, Silvia, Ciccone, Simona, Djurovic, Srdjan, Riedel-Heller, Steffi, Kuulasmaa, Teemu, del Ser, Teodoro, Ngandu, Tiia, García-Alberca, Jose María, Lleó, Alberto, Real, Luis M., Mir, Pablo, Scheltens, Philip, Holstege, Henne, Amouyel, Philippe, Blennow, Kaj, Andreassen, Ole A., Posthuma, Danielle

    Published in Nature communications
    Get full text
    Article
  18. 18
  19. 19
  20. 20

    Subcutaneous immunoglobulin for maintenance treatment in chronic inflammatory demyelinating polyneuropathy (PATH): a randomised, double-blind, placebo-controlled, phase 3 trial by van Schaik, Ivo N, Bril, Vera, van Geloven, Nan, Lewis, Richard A, Sobue, Gen, Lawo, John-Philip, Mielke, Orell, Durn, Billie L, Cornblath, David R, George, K., Henderson, R., Van Damme, P., Demeestere, J., Larue, S., D'Amour, C., Breiner, A., Kunc, P., Sussova, J., Kalous, T., Talab, R., Bednar, M., Toomsoo, T., Sorro, U., Saarela, M., Auranen, M., Pouget, J., Attarian, S., Le Masson, G., Wielanek-Bachelet, A., Delmont, E., Aufauvre, D., Sommer, C., Kramer, D., Goerlitz, C., Haas, J., Chatzopoulos, M., Gold, R., Jaspert-Grehl, A., Kutschenko, A., Trebst, C., Baum, P., Bergh, F., Klehmet, J., Klostermann, F., Oechtering, J., Schroeter, M., Mueller, D., Sperfeld, A., Drory, V., Algom, A., Yarnitsky, D., Murinson, B., Ciccocioppo, F., Grandis, M., Lauria, G., Cazzato, D., Antonini, G., Morino, S., Cocito, D., Zibetti, M., Yokota, T., Ohkubo, T., Kanda, T., Kaida, K., Onoue, H., Kuwabara, S., Mori, M., Iijima, M., Baba, M., Yokoyama, K., van Schaik, I.N., Visser, N., Hoeijmakers, J., Rejdak, K., Casanovas Pons, C., Alberti Aguiló, M., Figueras, M., Marquez Infante, C., Benitez Rivero, S., Lunn, M., Morrow, J., Lavin, T., Melamed, I., Ajroud-Driss, S., Menichella, D., Dimachkie, M., Beydoun, S., Johl, H., Shtilbans, A., Ladha, S., Freimer, M., Kissel, J., Latov, N., Ubogu, E., Rao, T., Sharma, K., Gonzalez, G., Allen, J., Walk, D., Hobson-Webb, L.

    Published in Lancet neurology
    Get full text
    Article