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Annals of Neurology, ISSN 0364-5134, 2014, Volume 76, Issue 1, pp. 120 - 133
Journal Article
Neurology, ISSN 0028-3878, 2012, Volume 79, Issue 10, pp. 962 - 964
Journal Article
by Davies, Gail and Armstrong, Nicola J and Bis, Joshua and Bressler, Jan and Chouraki, Vincent and Giddaluru, Sudheer and Hofer, E and Ibrahim-Verbaas, Carla and Kirin, Mirna and Lahti, J and Lee, Sven and Le Hellard, Stephanie and Liu, T and Marioni, Riccardo and Oldmeadow, Christopher and Postmus, Douwe and Smith, G.D and Smith, Jennifer A and Thalamuthu, Anbupalam and Thomson, Russell and Vitart, Veronique and Wang, J and Yu, L and Zgaga, Lina and Zhao, Wei and Boxall, Ruth and Harris, Sarah and Hill, W. David and Liewald, David C and Luciano, Michelle and Adams, Hieab and Ames, David and Amin, Najaf and Amouyel, Philippe and Assareh, A.A and Au, R and Becker, James and Beiser, A and Berr, Claudine and Bertram, Lars and Boerwinkle, Eric and Buckley, Brendan M and Campbell, Harry and Corley, J and De Jager, P.L and Dufouil, Carole and Eriksson, Johan G and Espeseth, Thomas and Faul, J.D and Ford, I and Scotland, Generation and Gottesman, Rebecca and Griswold, Michael and Gudnason, Vilmundur and Harris, T.B and Heiss, Gerardo and Hofman, Albert and Holliday, Elizabeth and Huffman, Jennifer and Kardia, Sharon and Kochan, Nicole A and Knopman, David and Kwok, J.B and Lambert, J.-C and Lee, T and Li, G and Li, S.-C and Loitfelder, Marisa and Lopez, Oscar and Lundervold, A.J and Lundqvist, A and Mather, R and Mirza, Saira and Nyberg, L and Oostra, Ben and Palotie, Aarno and Papenberg, G and Pattie, Alison and Petrovic, Katja and Polasek, Ozren and Psaty, Bruce and Redmond, Paul and Reppermund, S and Rotter, J.I and Schmidt, Reinhold and Schuur, Maaike and Schofield, P.W and Scott, R.J and Steen, Vidar and Stott, David J and Swieten, John and Taylor, Kent and Trollor, J and Trompet, Stella and Uitterlinden, Ané and Weinstein, G and Widen, Elisabeth and Windham, B Gwen and Jukema, Jan Wouter and Wright, Alan and ... and Generation Scotland and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Molecular Psychiatry, ISSN 1359-4184, 01/2015, Volume 20, Issue 2, pp. 183 - 192
Journal Article
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, ISSN 1552-4841, 2012, Volume 159B, Issue 6, pp. 628 - 643
With increased frequency, clinical geneticists are asked for genetic advice on the heredity of dementia in families. Alzheimer's disease is in most cases a... 
Journal Article
Journal Article
Neurology, ISSN 0028-3878, 2012, Volume 79, pp. 1377 - 1383
OBJECTIVE: The assessment of behavioral disturbances in amyotrophic lateral sclerosis (ALS) is important because of the overlap with the behavioral variant of... 
Journal Article
Neurology, ISSN 0028-3878, 2012, Volume 79, Issue 13, pp. 1377 - 1383
Objective: The assessment of behavioral disturbances in amyotrophic lateral sclerosis (ALS) is important because of the overlap with the behavioral variant of... 
Journal Article
Neurology, ISSN 0028-3878, 2012, Volume 79, Issue 13, pp. 1377 - 1383
Objective: The assessment of behavioral disturbances in amyotrophic lateral sclerosis (ALS) is important because of the overlap with the behavioral variant of... 
Journal Article
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 2011, Volume 82, Issue 5, pp. 476 - 486
Frontotemporal dementia (FTD) is the second most common young-onset dementia and is clinically characterised by progressive behavioural change, executive... 
Journal Article
Journal Article
European Journal of Neurology, ISSN 1351-5101, 2009, Volume 16, Issue 3, pp. 297 - 309
Tauopathies with parkinsonism represent a spectrum of disease entities unified by the pathologic accumulation of hyperphosphorylated tau protein fragments... 
Parkinsonism | Tauopathies | Progressive supranuclear palsy | Multiple system atrophy | Parkinson disease | Frontotemporal dementia with parkinsonism linked to chromosome 17 | Corticobasal degeneration | Microtubule-associated protein tau | TAU-PROTEIN | NEUROFIBRILLARY TANGLES | ATYPICAL PARKINSONISM | corticobasal degeneration | parkinsonism | ALZHEIMERS-DISEASE | GLYCOGEN-SYNTHASE KINASE-3 | FRONTOTEMPORAL DEMENTIA | frontotemporal dementia with parkinsonism linked to chromosome 17 | multiple system atrophy | NEUROSCIENCES | CLINICAL NEUROLOGY | microtubule-associated protein tau | MITOCHONDRIAL COMPLEX-I | MOUSE MODEL | tauopathies | progressive supranuclear palsy | TRANSGENIC MICE | Geography | Supranuclear Palsy, Progressive - physiopathology | Parkinsonian Disorders - complications | Humans | Tauopathies - pathology | Dementia - physiopathology | Dementia - genetics | Niemann-Pick Disease, Type C - physiopathology | Supranuclear Palsy, Progressive - complications | Pick Disease of the Brain - pathology | tau Proteins - genetics | Drug Design | Tauopathies - complications | Tauopathies - therapy | Niemann-Pick Disease, Type C - diagnosis | Tauopathies - physiopathology | Parkinsonian Disorders - physiopathology | Pick Disease of the Brain - complications | Parkinson Disease, Postencephalitic - physiopathology | Protein-Serine-Threonine Kinases - genetics | Parkinson Disease, Postencephalitic - complications | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 | Animals | Dementia - complications | Parkinsonian Disorders - pathology | Parkinsonian Disorders - therapy | Models, Biological | Biomarkers | Mutation | Niemann-Pick Disease, Type C - complications | Supranuclear Palsy, Progressive - diagnosis | Medical colleges | Care and treatment | Orphan drugs | Neurosciences | Parkinson's disease | Amyotrophic lateral sclerosis | Biological markers | Banks (Finance) | Natural history | microtubule-associated protein tau, multiple system atrophy | Review
Journal Article
by Ibrahim-Verbaas, Carla and Bressler, Jan and Debette, Stéphanie and Schuur, Maaike and Smith, A.V and Bis, Joshua and Davies, Gail and Trompet, Stella and Smith, J.A and Björnsson, Asgeir and Chibnik, Lori and Liu, Y and Vitart, Veronique and Kirin, Mirna and Petrovic, Katja and Polasek, Ozren and Zgaga, Lina and Fawns-Ritchie, C and Hoffmann, Per and Karjalainen, Juha and Lahti, J and Llewellyn, D.J and Schmidt, Carsten O and Mather, R and Chouraki, Vincent and Sun, Q and Resnick, S.M and Rose, Lynda and Oldmeadow, Christopher and Stewart, M and Smith, B.H and Gudnason, Vilmundur and Yang, Qiong and Mirza, Saira and Jukema, J.W and DeJager, Philip L and Harris, Tamara and Liewald, David C and Amin, Najaf and Coker, Laura and Stegle, Oliver and Lopez, O.L and Schmidt, R and Teumer, Alexander and Ford, I and Karbalai, Nazanin and Becker, James and Jonsdottir, Maria K and Au, Rhoda and Fehrmann, Rudolf and Herms, Stefan and Nalls, Michael and Zhao, W and Turner, Stephen and Yaffe, K and Lohman, Kurt and Swieten, John and Kardia, Sharon L.r and Knopman, David and Meeks, William and Heiss, Gerardo and Holliday, Elizabeth and Schofield, P.W and Tanaka, Toshiko and Stott, David J and Wang, Jing and Ridker, Paul and Gow, A.J and Pattie, Alison and Starr, John and Hocking, L.J and Armstrong, Nicola and McLachlan, Stela and Shulman, J.M and Pilling, Luke and Eiriksdottir, Gudny and Scott, Rodney and Kochan, Nicole A and Palotie, Aarno and Hsieh, Yi-Chen and Eriksson, Johan G and Penman, Alan and Gottesman, Rebecca and Oostra, Ben and Yu, Lei and DeStefano, Anita and Beiser, Alexa and Garcia, M and Rotter, Jerome I and Nöthen, Markus M and Hofman, Albert and Slagboom, Eline and Westendorp, R.G.J and Buckley, Brendan M and Wolf, P.A and Uitterlinden, Ané and Psaty, Bruce and Grabe, Hans Jörgen and Bandinelli, Stefania and Chasman, Daniel and ... and Generation Scotland and on behalf of Generation Scotland
Molecular Psychiatry, ISSN 1359-4184, 02/2016, Volume 21, Issue 2, pp. 189 - 197
Journal Article