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Frontotemporal dementia
Citations 11-20 of 114 total displayed.
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Past content
(since Aug 2001):
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- ARTICLES
Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His
- J. van der Zee, D. Pirici, T. Van Langenhove, S. Engelborghs, R. Vandenberghe, M. Hoffmann, G. Pusswald, M. Van den Broeck, K. Peeters, M. Mattheijssens, J. -J. Martin, P. P. De Deyn, M. Cruts, D. Haubenberger, S. Kumar-Singh, A. Zimprich, and C. Van Broeckhoven
Neurology 2009; 73: 626-632.
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- ARTICLES
Neurocognitive contributions to verbal fluency deficits in frontotemporal lobar degeneration
- D. J. Libon, C. McMillan, D. Gunawardena, C. Powers, L. Massimo, A. Khan, B. Morgan, C. Farag, L. Richmond, J. Weinstein, P. Moore, H. B. Coslett, A. Chatterjee, G. Aguirre, and M. Grossman
Neurology 2009; 73: 535-542.
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Familial aggregation of parkinsonism in progressive supranuclear palsy
- L. Donker Kaat, A.J.W. Boon, A. Azmani, W. Kamphorst, M. M.B. Breteler, B. Anar, P. Heutink, and J. C. van Swieten
Neurology 2009; 73: 98-105.
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Characterization of DCTN1 genetic variability in neurodegeneration
- C. Vilariño-Güell, C. Wider, A. I. Soto-Ortolaza, S. A. Cobb, J. M. Kachergus, B. H. Keeling, J. C. Dachsel, M. M. Hulihan, D. W. Dickson, Z. K. Wszolek, R. J. Uitti, N. R. Graff-Radford, B. F. Boeve, K. A. Josephs, B. Miller, K. B. Boylan, K. Gwinn, C. H. Adler, J. O. Aasly, F. Hentati, A. Destée, A. Krygowska-Wajs, M. -C. Chartier-Harlin, O. A. Ross, R. Rademakers, and M. J. Farrer
Neurology 2009; 72: 2024-2028.
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Brain and ventricular volumetric changes in frontotemporal lobar degeneration over 1 year
- D. S. Knopman, C. R. Jack, Jr, J. H. Kramer, B. F. Boeve, R. J. Caselli, N. R. Graff-Radford, M. F. Mendez, B. L. Miller, and N. D. Mercaldo
Neurology 2009; 72: 1843-1849.
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Atrophy patterns in histologic vs clinical groupings of frontotemporal lobar degeneration
- J.M.S. Pereira, G. B. Williams, J. Acosta-Cabronero, G. Pengas, M. G. Spillantini, J. H. Xuereb, J. R. Hodges, and P. J. Nestor
Neurology 2009; 72: 1653-1660.
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- ARTICLES
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
- I. Le Ber, A. Camuzat, E. Berger, D. Hannequin, A. Laquerrière, V. Golfier, D. Seilhean, G. Viennet, P. Couratier, P. Verpillat, S. Heath, W. Camu, O. Martinaud, L. Lacomblez, M. Vercelletto, F. Salachas, F. Sellal, M. Didic, C. Thomas-Anterion, M. Puel, B-F Michel, C. Besse, C. Duyckaerts, V. Meininger, D. Campion, B. Dubois, A. Brice For the French Research Network on FTD/FTD-MND
Neurology 2009; 72: 1669-1676.
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Patterns of cortical thinning in the language variants of frontotemporal lobar degeneration
- J. D. Rohrer, J. D. Warren, M. Modat, G. R. Ridgway, A. Douiri, M. N. Rossor, S. Ourselin, and N. C. Fox
Neurology 2009; 72: 1562-1569.
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Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN
- J. L. Whitwell, C. R. Jack, Jr, B. F. Boeve, M. L. Senjem, M. Baker, R. Rademakers, R. J. Ivnik, D. S. Knopman, Z. K. Wszolek, R. C. Petersen, and K. A. Josephs
Neurology 2009; 72: 813-820.
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Sensitivity of current criteria for the diagnosis of behavioral variant frontotemporal dementia
- O. Piguet, M. Hornberger, B. P. Shelley, C. M. Kipps, and J. R. Hodges
Neurology 2009; 72: 732-737.
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