Search Results - Halliday, Sandra M.

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    Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study by Nicholas, Jennifer, Grossman, Murray, McMillan, Corey T, Massimo, Lauren, Van Deerlin, Vivianna M, Warren, Jason D, Fox, Nick C, Bocchetta, Martina, Boeve, Bradley F, Knopman, David S, Rademakers, Rosa, van Swieten, John C, Meeter, Lieke H, Dopper, Elise GP, Snowden, Julie S, Saxon, Jennifer, Pickering-Brown, Stuart, Le Ber, Isabelle, Brice, Alexis, Caroppo, Paola, Ghidoni, Roberta, Pievani, Michela, Binetti, Giuliano, Dickerson, Bradford C, Lucente, Diane, Graff, Caroline, Ghoshal, Nupur, Galimberti, Daniela, Scarpini, Elio, Mackenzie, Ian R, Hsiung, Ging-Yuek R, Sengdy, Pheth, Boxer, Adam L, Taylor, Joanne B, Synofzik, Matthis, Wilke, Carlo, Sulzer, Patricia, Kwok, John, Lladó, Albert, Borrego-Ecija, Sergi, Santana, Isabel, Almeida, Maria Rosário, Tábuas-Pereira, Miguel, Moreno, Fermin, Barandiaran, Myriam, Indakoetxea, Begoña, Levin, Johannes, Danek, Adrian, Rowe, James B, Anderl-Straub, Sarah, Masellis, Mario, Black, Sandra E, Lautrette, Geraldine, Vandenberghe, Rik, Rogalski, Emily J, Weintraub, Sandra, Gerhard, Alexander, Onyike, Chiadi U, Papageorgiou, Sokratis G, Bras, Jose, Rohrer, Jonathan D, Heller, Carolin, Convery, Rhian S, Shafei, Rachelle M, Jones, David T, Baker, Matt, Gavrilova, Ralitza, Domoto-Reilly, Kimiko, Poos, Jackie M, Van der Ende, Emma L, Panman, Jessica L, Seelaar, Harro, Fostinelli, Silvia, Chiang, Huei-Hsin, Arighi, Andrea, Fenoglio, Chiara, Heuer, Hilary, Miller, Bruce, Karydas, Anna, Fong, Jamie, João Leitão, Maria, Santiago, Beatriz, Ferreira, Carlos, De Arriba, Maria, Tainta, Mikel, Zulaica, Miren, Ferreira, Catarina, Semler, Elisa, Ludolph, Albert, Miltenberger, Gabriel, Rogaeva, Ekaterina, Bruffaerts, Rose, Vandenbulcke, Mathieu, Mesulam, M Marsel, Bigio, Eileen, Kroupis, Christos, Stefanis, Leonidas, Shoesmith, Christien, Robertson, Erik, Geschwind, Daniel

    Published in Lancet neurology
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    MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study by Valentino, Rebecca R, Heckman, Michael G, Shoai, Maryam, Martinez-Carrasco, Alejandro, Tamvaka, Nicole, Walton, Ronald L, Real, Raquel, Mok, Kin, Christopher, Elizabeth A, Lee, Edward B, Frosch, Matthew P, Molina-Porcel, Laura, Gefen, Tamar, Robinson, Andrew C, Kobylecki, Christopher, Rowe, James B, Beach, Thomas G, Teich, Andrew F, Keith, Julia L, Bodi, Istvan, Gearing, Marla, Arzberger, Thomas, Morris, Christopher M, White, Charles L, Mechawar, Naguib, MacKenzie, Ian R, McLean, Catriona, Wang, Shih-Hsiu J, Nagra, Rashed M, Kovacs, Gabor G, Giaccone, Giorgio, Ang, Lee-Cyn, Morris, Huw R, Hardy, John A, Dickson, Dennis W, Ross, Owen A, Warner, Thomas T, Boeve, Bradley F, Duara, Ranjan, Josephs, Keith A, Murray, Melissa E, Lyons, Kelly E, Whitwell, Jennifer L, Miller, Bruce, Schlereth, Athena, Van Deerlin, Vivianna M, Wolk, David A, Connors, Theresa R, Dooley, Patrick M, Aldecoa, Iban, Gelpi, Ellen, Sánchez-Valle, Raquel, Sanz-Cartagena, Pilar, Bigio, Eileen H, Weintraub, Sandra, Schneider, Julie A, Chang, Koping, Troncoso, Juan C, Jones, Matthew, Richardson, Anna, Roncaroli, Federico, Snowden, Julie, Serrano, Geidy E, Goldman, James E, Leskinen, Sandra P, Masellis, Mario, King, Andrew, Al-Sarraj, Safa, Troakes, Claire, Hodges, John R, Kril, Jillian J, Kwok, John B, Roeber, Sigrun, Attems, Johannes, Thomas, Alan J, Evers, Bret M., Bieniek, Kevin F, Sieben, Anne A, Cras, Patrick P, De Vil, Bart B, Castellani, Rudolph J, Chaffee, Ann, Franklin, Erin, Jacobsen, Max, Keene, Dirk, Latimer, Caitlin S, Purohit, Dushyant P, Schantz, Aimee, Walker, Jamie, De Deyn, Peter P, Duyckaerts, Charles, Seilhean, Danielle, Turbant-Leclere, Sabrina, Nennesmo, Inger, Riehl, James, Nacmias, Benedetta, Finger, Elizabeth C, Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B

    Published in Lancet neurology
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    Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTL... by Pottier, Cyril, Ren, Yingxue, Perkerson, Ralph B., Baker, Matt, Jenkins, Gregory D., van Blitterswijk, Marka, DeJesus-Hernandez, Mariely, van Rooij, Jeroen G. J., Murray, Melissa E., Christopher, Elizabeth, McDonnell, Shannon K., Fogarty, Zachary, Batzler, Anthony, Tian, Shulan, Vicente, Cristina T., Matchett, Billie, Karydas, Anna M., Hsiung, Ging-Yuek Robin, Seelaar, Harro, Mol, Merel O., Finger, Elizabeth C., Graff, Caroline, Öijerstedt, Linn, Neumann, Manuela, Heutink, Peter, Synofzik, Matthis, Wilke, Carlo, Prudlo, Johannes, Rizzu, Patrizia, Simon-Sanchez, Javier, Edbauer, Dieter, Diehl-Schmid, Janine, Evers, Bret M., King, Andrew, Mesulam, M. Marsel, Weintraub, Sandra, Geula, Changiz, Bieniek, Kevin F., Petrucelli, Leonard, Ahern, Geoffrey L., Reiman, Eric M., Woodruff, Bryan K., Caselli, Richard J., Huey, Edward D., Farlow, Martin R., Grafman, Jordan, Mead, Simon, Grinberg, Lea T., Spina, Salvatore, Irwin, David J., Lee, Edward B., Suh, EunRan, Snowden, Julie, Mann, David, Ertekin-Taner, Nilufer, Uitti, Ryan J., Wszolek, Zbigniew K., Josephs, Keith A., Parisi, Joseph E., Knopman, David S., Petersen, Ronald C., Hodges, John R., Piguet, Olivier, Geier, Ethan G., Yokoyama, Jennifer S., Rissman, Robert A., Rogaeva, Ekaterina, Keith, Julia, Zinman, Lorne, Tartaglia, Maria Carmela, Cairns, Nigel J., Cruchaga, Carlos, Kofler, Julia, Lopez, Oscar L., Beach, Thomas G., Arzberger, Thomas, Herms, Jochen, Honig, Lawrence S., Vonsattel, Jean Paul, Halliday, Glenda M., Kwok, John B., White, Charles L., Gearing, Marla, Glass, Jonathan, Rollinson, Sara, Pickering-Brown, Stuart, Rohrer, Jonathan D., Trojanowski, John Q., Van Deerlin, Vivianna, Bigio, Eileen H., Troakes, Claire, Asmann, Yan, Miller, Bruce L., Boeve, Bradley F., Seeley, William W., Mackenzie, Ian R. A., van Swieten, John C., Dickson, Dennis W., Biernacka, Joanna M., Rademakers, Rosa

    Published in Acta neuropathologica
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