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Neurobiology of Aging, ISSN 0197-4580, 04/2019, Volume 76, pp. 214.e11 - 214.e15
Frontotemporal lobar degeneration caused by mutations is mainly associated with a TDP-43 type A proteinopathy. We present a family with autosomal dominant... 
Astrogliopathy | GRN mutations | ARTAG | Tauopathy | Neuropathology | PATHOLOGIES | PATTERNS | PROGRANULIN | NEUROSCIENCES | BRAIN | GERIATRICS & GERONTOLOGY | Proteins | Alzheimer's disease | Genetic aspects
Journal Article
by Pottier, Cyril and Zhou, Xiaolai and Perkerson, Ralph B and Baker, Matt and Jenkins, Gregory D and Serie, Daniel J and Ghidoni, Roberta and Benussi, Luisa and Binetti, Giuliano and López de Munain, Adolfo and Zulaica, Miren and Moreno, Fermin and Le Ber, Isabelle and Pasquier, Florence and Hannequin, Didier and Sánchez-Valle, Raquel and Antonell, Anna and Lladó, Albert and Parsons, Tammee M and Finch, NiCole A and Finger, Elizabeth C and Lippa, Carol F and Huey, Edward D and Neumann, Manuela and Heutink, Peter and Synofzik, Matthis and Wilke, Carlo and Rissman, Robert A and Slawek, Jaroslaw and Sitek, Emilia and Johannsen, Peter and Nielsen, Jørgen E and Ren, Yingxue and van Blitterswijk, Marka and DeJesus-Hernandez, Mariely and Christopher, Elizabeth and Murray, Melissa E and Bieniek, Kevin F and Evers, Bret M and Ferrari, Raffaele and Ferrari, Camilla and Rollinson, Sara and Richardson, Anna and Scarpini, Elio and Fumagalli, Giorgio G and Padovani, Alessandro and Hardy, John and Momeni, Parastoo and Frangipane, Francesca and Maletta, Raffaele and Anfossi, Maria and Gallo, Maura and Petrucelli, Leonard and Suh, EunRan and Lopez, Oscar L and Wong, Tsz H and van Rooij, Jeroen G J and Seelaar, Harro and Mead, Simon and Caselli, Richard J and Reiman, Eric M and Noel Sabbagh, Marwan and Kjolby, Mads and Nykjaer, Anders and Karydas, Anna M and Boxer, Adam L and Grinberg, Lea T and Grafman, Jordan and Spina, Salvatore and Oblak, Adrian and Mesulam, M-Marsel and Weintraub, Sandra and Geula, Changiz and Hodges, John R and Piguet, Olivier and Brooks, William S and Irwin, David J and Trojanowski, John Q and Lee, Edward B and Josephs, Keith A and Parisi, Joseph E and Ertekin-Taner, Nilüfer and Knopman, David S and Nacmias, Benedetta and Piaceri, Irene and Bagnoli, Silvia and Sorbi, Sandro and Gearing, Marla and Glass, Jonathan and Beach, Thomas G and Black, Sandra E and Masellis, Mario and Rogaeva, Ekaterina and Vonsattel, Jean-Paul and Honig, Lawrence S and Kofler, Julia and Bruni, Amalia C and Snowden, Julie and Mann, David and Pickering-Brown, Stuart and ...
The Lancet Neurology, ISSN 1474-4422, 06/2018, Volume 17, Issue 6, pp. 548 - 558
Journal Article
Journal of Alzheimer's Disease, ISSN 1387-2877, 2018, Volume 62, Issue 4, pp. 1683 - 1689
Background: During the twentieth century, frontotemporal dementia (FTD) was often misdiagnosed, confused with Alzheimer's disease or psychiatric disorders,... 
mutation | frontotemporal dementia | GRN | Alzheimer's disease | MISSENSE | DEMENTIA | CLINICAL-DIAGNOSIS | PHENOTYPE | TAU | NINCDS-ADRDA CRITERIA | PROGRANULIN | NEUROSCIENCES | PREDICTION | CHROMOSOME-17 | ASSOCIATION
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 12/2008, Volume 17, Issue 23, pp. 3631 - 3642
Journal Article
Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 01/2015, Volume 74, Issue 1, pp. 75 - 84
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2019
GRN null mutations are among the main genetic causes of frontotemporal dementia through progranulin haploinsufficiency. Most missense mutations are considered... 
GRN | Missense mutation | Progranulin | TDP-43 | Frontotemporal lobar degeneration | Frontotemporal dementia | C9orf72
Journal Article
Brain, ISSN 0006-8950, 02/2016, Volume 139, Issue 2, pp. 452 - 467
Journal Article
Journal Article
Journal Article