Treffer 1 - 20 von 238 für Suche 'King, Bradley H', Suchdauer: 1,36s Treffer weiter einschränken
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    NEK1 variants confer susceptibility to amyotrophic lateral sclerosis von Kenna, Kevin P, van Doormaal, Perry T C, Dekker, Annelot M, Ticozzi, Nicola, Kenna, Brendan J, Diekstra, Frank P, van Rheenen, Wouter, van Eijk, Kristel R, Jones, Ashley R, Keagle, Pamela, Shatunov, Aleksey, Sproviero, William, Smith, Bradley N, van Es, Michael A, Topp, Simon D, Kenna, Aoife, Miller, Jack W, Fallini, Claudia, Tiloca, Cinzia, McLaughlin, Russell L, Vance, Caroline, Troakes, Claire, Colombrita, Claudia, Mora, Gabriele, Calvo, Andrea, Verde, Federico, Al-Sarraj, Safa, King, Andrew, Calini, Daniela, de Belleroche, Jacqueline, Baas, Frank, van der Kooi, Anneke J, de Visser, Marianne, ten Asbroek, Anneloor L M A, Sapp, Peter C, McKenna-Yasek, Diane, Polak, Meraida, Asress, Seneshaw, Muñoz-Blanco, José Luis, Strom, Tim M, Meitinger, Thomas, Morrison, Karen E, Lauria, Giuseppe, Williams, Kelly L, Leigh, P Nigel, Nicholson, Garth A, Blair, Ian P, Leblond, Claire S, Dion, Patrick A, Rouleau, Guy A, Pall, Hardev, Shaw, Pamela J, Turner, Martin R, Talbot, Kevin, Taroni, Franco, Boylan, Kevin B, Van Blitterswijk, Marka, Rademakers, Rosa, Esteban-Pérez, Jesús, García-Redondo, Alberto, Van Damme, Phillip, Robberecht, Wim, Chio, Adriano, Gellera, Cinzia, Drepper, Carsten, Sendtner, Michael, Ratti, Antonia, Glass, Jonathan D, Mora, Jesús S, Basak, Nazli A, Hardiman, Orla, Ludolph, Albert C, Andersen, Peter M, Weishaupt, Jochen H, Brown, Robert H, Al-Chalabi, Ammar, Silani, Vincenzo, Shaw, Christopher E, van den Berg, Leonard H, Veldink, Jan H, Landers, John E

    Veröffentlicht in Nature genetics

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    Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS von Smith, Bradley N., Ticozzi, Nicola, Fallini, Claudia, Gkazi, Athina Soragia, Topp, Simon, Kenna, Kevin P., Scotter, Emma L., Kost, Jason, Keagle, Pamela, Miller, Jack W., Calini, Daniela, Vance, Caroline, Danielson, Eric W., Troakes, Claire, Tiloca, Cinzia, Al-Sarraj, Safa, Lewis, Elizabeth A., King, Andrew, Colombrita, Claudia, Pensato, Viviana, Castellotti, Barbara, de Belleroche, Jacqueline, Baas, Frank, ten Asbroek, Anneloor LMA, Sapp, Peter C., McKenna-Yasek, Diane, McLaughlin, Russell L., Polak, Meraida, Asress, Seneshaw, Esteban-Pérez, Jesús, Muñoz-Blanco, José Luis, Simpson, Michael, D’Alfonso, Sandra, Mazzini, Letizia, Comi, Giacomo P., Del Bo, Roberto, Ceroni, Mauro, Gagliardi, Stella, Querin, Giorgia, Bertolin, Cinzia, van Rheenen, Wouter, Diekstra, Frank P., Lauria, Giuseppe, Duga, Stefano, Corti, Stefania, Cereda, Cristina, Corrado, Lucia, Sorarù, Gianni, Morrison, Karen E., Williams, Kelly L., Nicholson, Garth A., Blair, Ian P., Dion, Patrick A., Leblond, Claire S., Rouleau, Guy A., Hardiman, Orla, Veldink, Jan H., van den Berg, Leonard H., Al-Chalabi, Ammar, Pall, Hardev, Shaw, Pamela J., Turner, Martin R., Talbot, Kevin, Taroni, Franco, García-Redondo, Alberto, Wu, Zheyang, Glass, Jonathan D., Gellera, Cinzia, Ratti, Antonia, Brown, Robert H., Silani, Vincenzo, Shaw, Christopher E., Landers, John E.

    Veröffentlicht in Neuron (Cambridge, Mass.)

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    Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis von Johnson, Janel O, Li, Rachel, Kumaran, Ravindran, Alahmady, Nada, Renton, Alan E, Topp, Simon D, Gibbs, J. Raphael, Cookson, Mark R, Troakes, Claire, Shatunov, Aleksey, Iacoangeli, Alfredo, Al Khleifat, Ahmad, Blair, Ian P, Kwok, John B, Bonkowski, Emily S, Shaw, Pamela J, Calvo, Andrea, Al-Saif, Hind, Leigh, Fawn, Scott, Anna I, Landers, John E, Chiò, Adriano, Crawford, Thomas O, Fallini, Claudia, Topp, Simon D, Keagle, Pamela, Pensato, Viviana, McLaughlin, Russell L, Stevic, Zorica, D’Alfonso, Sandra, Comi, Giacomo P, Del Bo, Roberto, Rademakers, Rosa, Corti, Stefania, Cereda, Cristina, Veldink, Jan H, van den Berg, Leonard H, García-Redondo, Alberto, Gellera, Cinzia, Ratti, Antonia, Viollet, Coralie, Hupalo, Daniel N, Ahmed, Sarah, Bowser, Robert, Brady, Christopher B, Campbell, Roy H, Cooper-Knock, John, Eicher, John D, Faghri, Faraz, Floeter, Mary Kay, Fratta, Pietro, Glass, Jonathan D, Hardy, John, Hernandez, Dena G, Jansson, Lilja, Laaksovirta, Hannu, Landi, Francesco, Le Ber, Isabelle, Lumbroso, Serge, Maragakis, Nicholas J, Nalls, Mike A, Rothstein, Jeffrey D, Sendtner, Michael, Sidle, Katie C, Simmons, Zachary, Troncoso, Juan C, Chiò, Adriano, Angelocola, Stefania M, Ausiello, Francesco P, Barberis, Marco, Bersano, Enrica, Borghero, Giuseppe, Brunetti, Maura, Canale, Fabrizio, Conforti, Francesca L, Dalla Bella, Eleonora, DeMarco, Giovanni, Filippi, Massimo, Fini, Nicola, Gallone, Salvatore, Grassano, Maurizio, Greco, Lucia, La Bella, Vincenzo, Lauria, Giuseppe, Logroscino, Giancarlo, Logullo, Francesco O, Lunetta, Christian, Mandrioli, Jessica, Marangi, Giuseppe, Marinou, Kalliopi, Marrosu, Maria Giovanna, Martinelli, Ilaria, Quattrini, Angelo, Salvi, Fabrizio, Sbaiz, Luca, Simonini, Cecilia, Tedeschi, Gioacchino, Volanti, Paolo, Zollino, Marcella, Zucchi, Elisabetta

    Veröffentlicht in JAMA neurology

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