Treffer 1 - 20 von 44 für Suche 'SEELEY, PATRICK JOHN', Suchdauer: 1,93s Treffer weiter einschränken
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    MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study von 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

    Veröffentlicht in Lancet neurology

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    Whole genome‐wide sequence analysis of long‐lived families (Long‐Life Family Study) identifies MTUS2 gene associated with late‐onset Alzheimer's disease von Vardarajan, Badri, Andersen, Stacy L., Thyagarajan, Bharat, Yashin, Anatoli, Krinsky‐McHale, Sharon, Handen, Benjamin L., Schupf, Nicole, Lee, Joseph H., Barral, Sandra, Bell, Karen, Bulova, Peter, Cohen, Ann D., Constantino, John N., Handen, Benjamin L., Head, Elizabeth, Honig, Lawrence, Ikonomovic, Milos D., Keator, David, Lao, Patrick, Lott, Ira T., Mapstone, Mark, Parisi, Melissa, Pulsifer, Margaret, Varadarajan, Badri, Zaman, Shahid, Adams, Perrie M., Allen, Mariet, Atwood, Craig S., Ayres, Gayle, Barral, Sandra, Beecham, Gary W., Biber, Sarah A., Boeve, Bradley F., Bush, William S., Byrd, Goldie, Chan, Kwun C., Chen, Yen‐Chi, Chesselet, Marie‐Francoise, Chin, Nathaniel A., Cranney, Marissa, Cruchaga, Carlos, DeToledo, John C., Ertekin‐Taner, Nilufer, Faber, Kelley M., Fallin, Daniele, Farrer, Lindsay A., Galasko, Douglas R., Gefen, Tamar, Goate, Alison M., Grabowski, Thomas, Haines, Jonathan L., Hakonarson, Hakon, Hall, Kathleen, Hall, James R., Harari, Oscar, Honig, Lawrence S., Hyman, Bradley T., Hynan, Linda, Johnson, Kimberly, Jun, Gyungah, Kamboh, M. Ilyas, Khaleeq, Aisha, Kunkle, Brian W., LaFerla, Frank M., Lah, James J., Lieberman, Andrew P., Lipton, Richard B., Lopez, Oscar L., Marquez, David, Marson, Daniel C., Masurkar, Arjun V., Mukherjee, Shubhabrata, Nudelman, Kelley, Parisi, Joseph E., Pavlik, Valory, Perez, Victoria, Petersen, Ronald C., Polk, Marsha, Qu, Liming, Quiceno, Mary, Raj, Ashok, Rajabli, Farid, Roberson, Erik D., Royall, Donald R., Sano, Mary, Song, Yeunjoo, George‐Hyslop, Peter St, Stern, Robert A., Stevens, Alan, Sultzer, David, Valladares, Otto, Van Deerlin, Vivianna M., Vance, Jeffery M., Vassar, Robert, Welsh‐Bohmer, Kathleen A., Wilms, Henrick, Wisniewski, Thomas, Woon, Martin, Younkin, Steven G., Zhu, Congcong

    Veröffentlicht in Alzheimer's & dementia

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    Studying the natural history of frontotemporal lobar degeneration (FTLD): The ARTFL LEFFTDS longitudinal FTLD (ALLFTD) protocol von Boeve, Bradley F., Boxer, Adam L., Rosen, Howard J., Forsberg, Leah K., Heuer, Hilary W., Brushaber, Danielle, Appleby, Brian, Biernacka, Joanna M., Bordelon, Yvette M., Botha, Hugo, Brannelly, Patrick, Dickerson, Brad C., Dickson, Dennis W., Kimiko, Domoto‐Reilly, Faber, Kelley, Fagan, Anne, Fields, Julie A., Fishman, Ann, Foroud, Tatiana M., Galasko, Doug R., Gavrilova, Ralitza H., Gendron, Tania F., Geschwind, Daniel H., Ghoshal, Nupur, Goldman, Jill, Graff‐Radford, Jonathan, Graff‐Radford, Neill R., Grant, Ian, Grossman, Murray, Hsiung, Ging‐Yuek Robin, Huang, Eric J., Huey, Edward, Irwin, David J., Jones, David T., Kantarci, Kejal, Karydas, Anna M., Kaufer, Daniel, Knopman, David S., Kramer, Joel H., Kremers, Walter K., Kornak, John, Kukull, Walter A., Lagone, Emma, Leger, Gabriel C., Litvan, Irene, Ljubenkov, Peter A., Lucente, Diane E, Mackenzie, Ian R, Manoochehri, Masood, Masdeu, Joseph C., McGinnis, Scott, Mendez, Mario F., Miller, Bruce L., Miyagawa, Toji, Nelson, Kevin M., Onyike, Chiadi U, Pantelyat, Alex, Pascual, Belen, Pearlman, Rodney, Petrucelli, Leonard, Rademakers, Rosa, Ramos, Eliana Marisa, Rankin, Katherine, Rascovsky, Katya, Rexach, Jessica E., Ritter, Aaron, Roberson, Erik D., Rojas, Julio C., Sabbagh, Marwan N., Salmon, David P., Savica, Rodolfo, Seeley, William W., Staffaroni, Adam M., Syrjanen, Jeremy, Tartaglia, Carmela, Tatton, Nadine, Taylor, Joanne, Toga, Arthur W., Weintraub, Sandra, Wheaton, Diana, Wong, Bonnie, Wszolek, Zbigniew

    Veröffentlicht in Alzheimer's & dementia

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