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frontotemporal bvftd disease inclusion frontotemporal lobar degeneration dementia pathology mutation frontotemporal dementia degeneration aftld-u lobar neuropathol department ftld-fu subtype protein mackenzie university ftld-up neurology ftld-ups cases aftld-u cases patient research symptom centre mackenzie ir fus pathology -43 ftld cases neurol family history family filament inclusion disease group ubiquitin hospital trojanowski study neumann dickson neuropathology variant ucl institute neumann m trojanowski jq ubiquitin-positive bigio institute cause rademakers r motor tdp -43 isaac baker m brain inclusion body disease onset chromosome medicine chmp 2b mutation rademaker diagnosis queen square grossman m neary revesz t feature broeckhoven kumar-singh mayo clinic snowden js snowden aftld-u subtype adamson j progranulin vandenberghe r nifid rossor mn
6 Most Recent Publications
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Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
(Article)
Hoglinger, G. Melhem, N.M. Swieten, J.C. van Pahwa, R. Pezzoli, G. Pickering-Brown, S. Poewe, W. Rabano, A. Rajput, A. Reich, S.G. Respondek, G. Roeber, S. Rohrer, J.D. Heutink, P. Ross, O.A. Rossor, M. Sacilotto, G. Seeley, W.W. Seppi, K. Silveira-Moriyama, L. Spina, S. Srulijes, K. St. George-Hyslop, P. Stamelou, M. Wszolek, Z.K. Standaert, D.G. Tesei, S. Tourtellotte, W.W. Trenkwalder, C. Troakes, C. Trojanowski, J.Q. Troncoso, J.C. Deerlin, V.M. Vonsattel, J.P.G. Wenning, G.K. Uitti, R.J. White, C.L. Winter, P. Zarow, C. Zecchinelli, A.L. Antonini, A. Vandrovcova, J. Hurtig, H.I. Gross, R.G. Maetzler, W. Goldwurm, S. Tolosa, E. Dickson, D. Borroni, B. Pastor, P. Cantwell, L.B. Han, M.R. Dillman, A. Brug, M.P. van der Gibbs, J. Cookson, M.R. Hernandez, D.G. Singleton, A. Sleiman, P.M.A. Farrer, M.J. Yu, C.-E. Golbe, L.I. Revesz, T. Hardy, J. Lees, A.J. Devlin, B. Hakonarson, H. Müller, U. Schellenberg, G.D. Wang, L.-S. Albin, R.L. Alonso, E. Apfelbacher, M. Arnold, S.E. Avila, J. Beach, T.G. Beecher, S. Berg, D. Bird, T.D. Bogdanovic, N. Klei, L. Boon, A.J.W. Bordelon, Y. Brice, A. Budka, H. Canesi, M. Chiu, W.Z. Cilia, R. Colosimo, C. Deyn, P.P. de Yebenes, J.G. de Rademakers, R. Donker Kaat, L. Duara, R. Durr, A. Engelborghs, S. Fabbrini, G. Finch, N.A. Flook, R. Frosch, M.P. Gaig, C. Galasko, D. Silva, R. de Gasser, T. Gearing, M. Geller, E.T. Ghetti, B. Graff-Radford, N.R. Grossman, M. Hall, D.A. Hazrati, L.-N. Höllerhage, M. Jankovic, J. Litvan, I. Juncos, J.L. Karydas, A. Kretzschmar, H.A. Leber, I. Lee, V.M.Y. Lieberman, A.P. Lyons, K.E. Mariani, C. Masliah, E. Massey, L.A. Riley, D.E. McLean, C.A. Meucci, N. Miller, B.L. Mollenhauer, B. Möller, J.C. Morris, H. O'Sullivan, S.S. Oertel, W. Ottaviani, D. Padovani, A. |
2011-07-01
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Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
(Article)
Hollingworth, P. Harold, D. Dowzell, K. Tikka-Kleemola, P. Breteler, M.M.B. Ikram, M.A. DeStefano, A.L. Fitzpatrick, A.L. Lopez, O.L. Launer, L.J. Seshadri, S. Berr, C. Campion, D. Jones, N. Epelbaum, J. Dartigues, J.-F. Tzourio, C. Alperovitch, A. Lathrop, G.M. Feulner, T.M. Friedrich, P. Riehle, C. Krawczak, M. Schreiber, S. Stretton, A. Mayhaus, M. Nicolhaus, S. Wagenpfeil, S. Steinberg, S. Kallela, M. SnÆdal, J. Björnsson, S. Jonsson, P.V. Chouraki, V. Genier-Boley, B. Thomas, C. Hiltunen, M. Soininen, H. Combarros, O. Zelenika, D. Delepine, M. Bullido, M.J. Pasquier, F. Mateo, I. Frank-Garcia, A. Porcellini, E. Richards, A. Hanon, O. Coto, E. Alvarez, V. Bosco, P. Siciliano, G. Mancuso, M. Panza, F. Solfrizzi, V. Nacmias, B. Sorbi, S. Ivanov, D. Bossù, P. Piccardi, P. Arosio, B. Annoni, G. Seripa, D. Pilotto, A. Scarpini, E. Galimberti, D. Brice, A. Hannequin, D. Widdowson, C. Licastro, F. Holmans, P.A. Riemenschneider, M. Morgan, K. Younkin, S. Owen, M.J. O'Donovan, M. Amouyel, P. Williams, J. Chapman, J. Lovestone, S. Powell, J. Sims, R. Proitsi, P. Lupton, M.K. Brayne, C. Rubinsztein, D.C. Gill, M. Lawlor, B. Lynch, A. Brown, K. Passmore, P.A. Craig, D. Gerrish, A. McGuinness, B. Todd, S. Holmes, C. Mann, D. Smith, A.D. Beaumont, H. Warden, D.R. Wilcock, G.K. Love, S. Kehoe, P.G. Lambert, J.C. Hooper, N.M. Vardy, E.R.L.C. Hardy, J. Mead, S. Fox, N.C. Rossor, M. Collinge, J. Maier, W. Jessen, F. Rüther, E. Carrasquillo, M.M. Schürmann, B. Heun, R. Kölsch, H. Bussche, H. van den Heuser, I. Kornhuber, J. Wiltfang, J. Dichgans, M. Frölich, L. Hampel, H. Abraham, R. Gallacher, J. Hüll, M. Rujescu, D. Giegling, I. Goate, A.M. Kauwe, J.S.K. Cruchaga, C. Nowotny, P. Morris, J.C. Mayo, K. Hamshere, M.L. Sleegers, K. Bettens, K. Engelborghs, S. Deyn, P.P. de Broeckhoven, C. van Livingston, G. Bass, N.J. Gurling, H. McQuillin, A. Gwilliam, R. Pahwa, J.S. Deloukas, P. Al-Chalabi, A. Shaw, C.E. Tsolaki, M. Singleton, A.B. Guerreiro, R. Mühleisen, T.W. Nöthen, M.M. Moebus, S. Jöckel, K.-H. Moskvina, V. Klopp, N. Wichmann, H.E. Pankratz, V.S. Sando, S.B. Aasly, J.O. Barcikowska, M. Wszolek, Z.K. Dickson, D. Graff-Radford, N.R. Petersen, R.C. |
2011-05-01
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Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration
(Article)
Chen-Plotkin, A. Martinez-Lage, M. Weiner, M.F. White, C.L. Brooks, W.S. Halliday, G.M. Kril, J.J. Gearing, M. Beach, T.G. Graff-Radford, N.R. Dickson, D. Rademakers, R. Sleiman, P.M.A. Boeve, B.F. Pickering-Brown, S. Snowden, J. Swieten, J.C. van Heutink, P. Seelaar, H. Murrell, J.R. Ghetti, B. Spina, S. Grafman, J. Hu, W.T. Kaye, J.A. Woltjer, R.L. Mesulam, M. Bigio, E.H. Lladó, A. Miller, B.L. Alzualde, A. Moreno, F. Rohrer, J.D. Mackenzie, I.R.A. Greene, R. Feldman, H.H. Hamilton, R.L. Cruts, M. Engelborghs, S. Deyn, P.P. de Broeckhoven, C. van Bird, T.D. Cairns, N.J. Goate, A.M. Frosch, M.P. Wood, E.M. Riederer, P.F. Bogdanovic, N. Lee, V.M.Y. Trojanowski, J.Q. Deerlin, V.M. Bing, S. Grossman, M. Schellenberg, G.D. Hatanpaa, K.J. |
2011-04-01
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Serum N-glycan profile shift during human ageing
(Article)
Vanhooren, V. Dewaele, S. Jaspers, K. Pluijm, I. van der Hoeijmakers, J.H.J. Chen, C.C. Libert, C. Engelborghs, S. Deyn, P.P. de Toussaint, O. Debacq-Chainiaux, F. Poulain, M. Glupczynski, Y. Franceschi, C. |
2010-10-01
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FUS pathology defines the majority of tau-and TDP-43-negative frontotemporal lobar degeneration
(Article)
Urwin, H. Josephs, K.A. Nielsen, J.E. Holm, I.E. Dickson, D. Rademakers, R. Graff-Radford, N.R. Parisi, J.E. Petersen, R.C. Hatanpaa, K.J. White Iii, C.L. Weiner, M.F. Rohrer, J.D. Geser, F. Deerlin, V.M. Trojanowski, J.Q. Miller, B.L. Seeley, W.W. Zee, J. van der Kumar-Singh, S. Engelborghs, S. Deyn, P.P. de Broeckhoven, C. van Mackenzie, I.R.A. Bigio, E.H. Deng, H-X. Halliday, G.M. Kril, J.J. Munoz, D.G. Mann, D. Pickering-Brown, S. Doodeman, V. Adamson, G. Ghazi-Noori, S Neumann, H.A.M. Fisher, E.M.C Holton, J.L. Revesz, T. Rossor, M.N. Collinge, J. Mead, S. Isaacs, A.M. Authier, A. Seelaar, H. Swieten, J.C. van Brown, J.M. Johannsen, P. |
2010-07-01
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Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
(Article)
Haugarvoll, K. Rademakers, R. Guidi, M. Riboldazzi, G. Brown, L. Walter, U. Benecke, R. Berg, D. Gasser, T. Theuns, J. Pals, P. Cras, P. Kachergus, J. Deyn, P.P. de Engelborghs, S. Pickut, B. Uitti, R.J. Foroud, T. Nichols, W.C. Hagenah, J. Klein, C. Samii, A. Zabetian, C.P. Nuytemans, K. Bonifati, V. Broeckhoven, C. van Farrer, M.J. Wszolek, Z.K. Ross, O.A. Gibson, J.M. Tan, E.K. Gaig, C. Tolosa, E. Goldwurm, S. |
2008-04-01
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