المؤلفون: Van Deerlin, Vivianna M, Sleiman, Patrick MA, Martinez-Lage, Maria, Chen-Plotkin, Alice, Wang, Li-San, Graff-Radford, Neill R, Dickson, Dennis W, Rademakers, Rosa, Boeve, Bradley F, Grossman, Murray, Arnold, Steven E, Mann, David MA, Pickering-Brown, Stuart M, Seelaar, Harro, Heutink, Peter, van Swieten, John C, Murrell, Jill R, Ghetti, Bernardino, Spina, Salvatore, Grafman, Jordan, Hodges, John, Spillantini, Maria Grazia, Gilman, Sid, Lieberman, Andrew P, Kaye, Jeffrey A, Woltjer, Randall L, Bigio, Eileen H, Mesulam, Marsel, al-Sarraj, Safa, Troakes, Claire, Rosenberg, Roger N, White, Charles L, Ferrer, Isidro, Lladó, Albert, Neumann, Manuela, Kretzschmar, Hans A, Hulette, Christine Marie, Welsh-Bohmer, Kathleen A, Miller, Bruce L, Alzualde, Ainhoa, de Munain, Adolfo Lopez, McKee, Ann C, Gearing, Marla, Levey, Allan I, Lah, James J, Hardy, John, Rohrer, Jonathan D, Lashley, Tammaryn, Mackenzie, Ian RA, Feldman, Howard H, Hamilton, Ronald L, Dekosky, Steven T, van der Zee, Julie, Kumar-Singh, Samir, Van Broeckhoven, Christine, Mayeux, Richard, Vonsattel, Jean Paul G, Troncoso, Juan C, Kril, Jillian J, Kwok, John BJ, Halliday, Glenda M, Bird, Thomas D, Ince, Paul G, Shaw, Pamela J, Cairns, Nigel J, Morris, John C, McLean, Catriona Ann, DeCarli, Charles, Ellis, William G, Freeman, Stefanie H, Frosch, Matthew P, Growdon, John H, Perl, Daniel P, Sano, Mary, Bennett, David A, Schneider, Julie A, Beach, Thomas G, Reiman, Eric M, Woodruff, Bryan K, Cummings, Jeffrey, Vinters, Harry V, Miller, Carol A, Chui, Helena C, Alafuzoff, Irina, Hartikainen, Päivi, Seilhean, Danielle, Galasko, Douglas, Masliah, Eliezer, Cotman, Carl W, Tuñón, M Teresa, Martínez, M Cristina Caballero, Munoz, David G, Carroll, Steven L, Marson, Daniel, Riederer, Peter F, Bogdanovic, Nenad, Schellenberg, Gerard D, Hakonarson, Hakon, Trojanowski, John Q, Lee, Virginia M-Y

المصدر: Nature Genetics. 42(3)

مصطلحات موضوعية: Biological Sciences, Genetics, Frontotemporal Dementia (FTD), Neurodegenerative, Dementia, Rare Diseases, Brain Disorders, Neurosciences, Acquired Cognitive Impairment, Aetiology, 2.1 Biological and endogenous factors, Case-Control Studies, Chromosomes, Human, Pair 7, DNA-Binding Proteins, Frontotemporal Lobar Degeneration, Gene Frequency, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Inclusion Bodies, Intercellular Signaling Peptides and Proteins, Linkage Disequilibrium, Membrane Proteins, Polymorphism, Single Nucleotide, Progranulins, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/6dm6028c

المؤلفون: Ingelsson, Martin, Ramasamy, Karunya, Russ, Carsten, Freeman, Stefanie H., Orne, Jennifer, Raju, Susan, Matsui, Toshifumi, Growdon, John H., Frosch, Matthew P., Ghetti, Bernardino, Brown, Robert H., Irizarry, Michael C., Hyman, Bradley T.

المصدر: Acta Neuropathologica. November 2007 114(5):471-479

المؤلفون: Skoglund, Lena, Matsui, Toshifumi, Freeman, Stefanie H, Wallin, Anders, 1950, Blom, Elin S, Frosch, Matthew P, Growdon, John H, Hyman, Bradley T, Lannfelt, Lars, Ingelsson, Martin, Glaser, Anna

المصدر: Alzheimer disease and associated disorders. 25(2):173-8

مصطلحات موضوعية: Psychiatry, Psykiatri

URL الوصول: https://gup.ub.gu.se/publication/144133

المؤلفون: Skoglund, Lena, Ingvast, Sofie, Matsui, Toshifumi, Freeman, Stefanie H., Frosch, Matthew P., Brundin, Rosemarie, Giedraitis, Vilmantas, Growdon, John H., Hyman, Bradley T., Lannfelt, Lars, Ingelsson, Martin, Glaser, Anna

المصدر: Dementia and Geriatric Cognitive Disorders. 28(5):471-475

مصطلحات موضوعية: Frontotemporal lobar degeneration, Frontotemporal dementia, Progranulin, Tau, Gene dosage alterations

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:du-13165

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