Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Mackenzie, Ian RA"'
Publikováno v:
In Lancet Neurology 2010 9(10):995-1007
Autor:
Chu, Stephanie A, Flagan, Taru M, Staffaroni, Adam M, Jiskoot, Lize C, Deng, Jersey, Spina, Salvatore, Zhang, Liwen, Sturm, Virginia E, Yokoyama, Jennifer S, Seeley, William W, Papma, Janne M, Geschwind, Dan H, Rosen, Howard J, Boeve, Bradley F, Boxer, Adam L, Heuer, Hilary W, Forsberg, Leah K, Brushaber, Danielle E, Grossman, Murray, Coppola, Giovanni, Dickerson, Bradford C, Bordelon, Yvette M, Faber, Kelley, Feldman, Howard H, Fields, Julie A, Fong, Jamie C, Foroud, Tatiana, Gavrilova, Ralitza H, Ghoshal, Nupur, Graff-Radford, Neill R, Hsiung, Ging-Yuek Robin, Huey, Edward D, Irwin, David J, Kantarci, Kejal, Kaufer, Daniel I, Karydas, Anna M, Knopman, David S, Kornak, John, Kramer, Joel H, Kukull, Walter A, Lapid, Maria I, Litvan, Irene, Mackenzie, Ian RA, Mendez, Mario F, Miller, Bruce L, Onyike, Chiadi U, Pantelyat, Alexander Y, Rademakers, Rosa, Marisa Ramos, Eliana, Roberson, Erik D, Carmela Tartaglia, Maria, Tatton, Nadine A, Toga, Arthur W, Vetor, Ashley, Weintraub, Sandra, Wong, Bonnie, Wszolek, Zbigniew K, ARTFL/LEFFTDS Consortium, Van Swieten, John C, Lee, Suzee E
Publikováno v:
Annals of clinical and translational neurology, vol 8, iss 1
ObjectiveMAPT mutations typically cause behavioral variant frontotemporal dementia with or without parkinsonism. Previous studies have shown that symptomatic MAPT mutation carriers have frontotemporal atrophy, yet studies have shown mixed results as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::80fe25a543bb2432ebaa60d869646bcb
https://escholarship.org/uc/item/6wz5f59w
https://escholarship.org/uc/item/6wz5f59w
Publikováno v:
Alzheimer disease and associated disorders, vol 34, iss 4
Cerebrospinal fluid (CSF) biomarkers amyloid-β and tau have been validated for the antemortem diagnosis of Alzheimer disease (AD) and are included in the AT(N) research framework for AD. Recently, an AT(N) CSF profile has been described for dementia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::c28c90bd326d61999a76f1b126f71bba
https://escholarship.org/uc/item/3mh5t8d7
https://escholarship.org/uc/item/3mh5t8d7
Autor:
Chen, Qin, Boeve, Bradley F, Schwarz, Christopher G, Reid, Robert, Tosakulwong, Nirubol, Lesnick, Timothy G, Bove, Jessica, Brannelly, Patrick, Brushaber, Danielle, Coppola, Giovanni, Dheel, Christina, Dickerson, Bradford C, Dickinson, Susan, Faber, Kelley, Fields, Julie, Fong, Jamie, Foroud, Tatiana, Forsberg, Leah, Gavrilova, Ralitza H, Gearhart, Debra, Ghoshal, Nupur, Goldman, Jill, Graff-Radford, Jonathan, Graff-Radford, Neill R, Grossman, Murray, Haley, Dana, Heuer, Hilary W, Hsiung, Ging-Yuek R, Huey, Edward, Irwin, David J, Jack, Clifford R, Jones, David T, Jones, Lynne, Karydas, Anna M, Knopman, David S, Kornak, John, Kramer, Joel, Kremers, Walter, Kukull, Walter A, Lapid, Maria, Lucente, Diane, Lungu, Codrin, Mackenzie, Ian RA, Manoochehri, Masood, McGinnis, Scott, Miller, Bruce L, Pearlman, Rodney, Petrucelli, Leonard, Potter, Madeline, Rademakers, Rosa, Ramos, Eliana M, Rankin, Katherine P, Rascovsky, Katya, Sengdy, Pheth, Shaw, Leslie, Syrjanen, Jeremy, Tatton, Nadine, Taylor, Joanne, Toga, Arthur W, Trojanowski, John, Weintraub, Sandra, Wong, Bonnie, Boxer, Adam L, Rosen, Howie, Wszolek, Zbigniew, Kantarci, Kejal, LEFFTDS Consortium
Our aim was to investigate the patterns and trajectories of white matter (WM) diffusion abnormalities in microtubule-associated protein tau (MAPT) mutations carriers. We studied 22 MAPT mutation carriers (12 asymptomatic, 10 symptomatic) and 20 nonca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::864b1ecf83209c11761fe2209b881e24
https://escholarship.org/uc/item/36k2s219
https://escholarship.org/uc/item/36k2s219
Publikováno v:
Journal of Neuroinflammation, Vol 4, Iss 1, p 7 (2007)
Abstract Progranulin (PGRN) is a pleiotropic protein that has gained the attention of the neuroscience community with recent discoveries of mutations in the gene for PGRN that cause frontotemporal lobar degeneration (FTLD). Pathogenic mutations in PG
Externí odkaz:
https://doaj.org/article/037209a55cf44bd599c6b5cad81e3184
Autor:
Boxer, Adam, Rosen, Howard, Boeve, Bradley, Heuer, Hilary, Coppola, Giovanni, Dickerson, Bradford, Bordelon, Yvette, Conwit, Robin, Dheel, Christina, Faber, Kelley, Feldman, Howard, Fields, Julie, Fong, Jamie, Foroud, Tatiana, Ghoshal, Nupur, Graff-Radford, Neill, Grossman, Murray, Hsiung, Ging-Yuek, Huey, Edward, Irwin, David, Kantarci, Kejal, Kaufer, Daniel, Karydas, Anna, Knopman, David, Komak, John, Kramer, Joel, Kukull, Walter, Litvan, Irene, Mackenzie, Ian RA, Mendez, Mario, Miller, Bruce, Miller, Matt, Miller, Matthew, Onyike, Chiadi, Pantelyat, Alexander, Potter, Madeline, Rademakers, Rosa, Roberson, Erik, Sutherland, Margaret, Tartaglia, Carmela, Toga, Arthur, Vetor, Ashley, Weintraub, Sandra, Wszolek, Zbigniew
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::9c6c45bd26f3a775373e15018640b17b
https://escholarship.org/uc/item/76x7g8xh
https://escholarship.org/uc/item/76x7g8xh
Autor:
Ferrari, Raffaele, Hernandez, Dena G, Nalls, Michael A, Rohrer, Jonathan D, Ramasamy, Adaikalavan, Kwok, John BJ, Dobson-Stone, Carol, Brooks, William S, Schofield, Peter R, Halliday, Glenda M, Hodges, John R, Piguet, Olivier, Bartley, Lauren, Thompson, Elizabeth, Haan, Eric, Hernández, Isabel, Ruiz, Agustín, Boada, Mercè, Borroni, Barbara, Padovani, Alessandro, Cruchaga, Carlos, Cairns, Nigel J, Benussi, Luisa, Binetti, Giuliano, Ghidoni, Roberta, Forloni, Gianluigi, Galimberti, Daniela, Fenoglio, Chiara, Serpente, Maria, Scarpini, Elio, Clarimón, Jordi, Lleó, Alberto, Blesa, Rafael, Waldö, Maria Landqvist, Nilsson, Karin, Nilsson, Christer, Mackenzie, Ian RA, Hsiung, Ging-Yuek R, Mann, David MA, Grafman, Jordan, Morris, Christopher M, Attems, Johannes, Griffiths, Timothy D, McKeith, Ian G, Thomas, Alan J, Pietrini, P, Huey, Edward D, Wassermann, Eric M, Baborie, Atik, Jaros, Evelyn, Tierney, Michael C, Pastor, Pau, Razquin, Cristina, Ortega-Cubero, Sara, Alonso, Elena, Perneczky, Robert, Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Kurz, Alexander, Rainero, Innocenzo, Rubino, Elisa, Pinessi, Lorenzo, Rogaeva, Ekaterina, St George-Hyslop, Peter, Rossi, Giacomina, Tagliavini, Fabrizio, Giaccone, Giorgio, Rowe, James B, Schlachetzki, Johannes CM, Uphill, James, Collinge, John, Mead, Simon, Danek, Adrian, Van Deerlin, Vivianna M, Grossman, Murray, Trojanowski, John Q, van der Zee, Julie, Deschamps, William, Van Langenhove, Tim, Cruts, Marc, Van Broeckhoven, Christine, Cappa, Stefano F, Le Ber, Isabelle, Hannequin, Didier, Golfier, Véronique, Vercelletto, Martine, Brice, Alexis, Nacmias, Benedetta, Sorbi, Sandro, Bagnoli, Silvia, Piaceri, Irene, Nielsen, Jørgen E, Hjermind, Lena E, Riemenschneider, Matthias, Mayhaus, Manuel, Ibach, Bernd, Gasparoni, Gilles, Pichler, Sabrina, Gu, Wei, Rossor, Martin N
Publikováno v:
The Lancet. Neurology, vol 13, iss 7
BackgroundFrontotemporal dementia (FTD) is a complex disorder characterised by a broad range of clinical manifestations, differential pathological signatures, and genetic variability. Mutations in three genes-MAPT, GRN, and C9orf72--have been associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::fa988b37ab528ab55edd967b5491da98
https://escholarship.org/uc/item/9t62224n
https://escholarship.org/uc/item/9t62224n
Akademický článek
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Autor:
Mackenzie, Ian RA, Rademakers, Rosa
Publikováno v:
Current Opinion in Neurology; December 2008, Vol. 21 Issue: 6 p693-700, 8p
Publikováno v:
Lancet Neurology. Oct2010, Vol. 9 Issue 10, p955-955. 1p.