View Author
frontotemporal inclusion patient frontotemporal lobar degeneration ftld-fu bvftd disease dementia family history caudate atrophy degeneration mutation frontotemporal dementia atrophy pathology lobar onset caudate neuropathol subtype family protein brain department aftld-u history -43 university ubiquitin neurol study neurology filament inclusion disease feature mackenzie -43-negative ftld-up ubiquitin-positive tdp -43 symptom group ftld-ups cases caudate nucleus ftld-u motor aftld-u cases inclusion body disease tdp -43-negative inclusions research centre mackenzie ir fus pathology ftld-fus cases behavioural center progranulin ftld cases frequency motor neuron disease ?? ?? hospital trojanowski neumann dickson antibody neuropathology variant ucl institute neumann m executive functions substantia nigra trojanowski jq bigio institute cause rademakers r isaac baker m nucleus chromosome
10 Most Recent Publications
|
Symmetrical corticobasal syndrome caused by a novel c.314dup progranulin mutation
(Article)
Dopper, E.G.P. Seelaar, H. Chiu, W.Z. Koning, I. de Minkelen, R. van Baker, M.C. Rozemuller, A.J.M. Rademakers, R. Swieten, J.C. van |
2011-11-01
|
|
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
(Article)
Renton, A. Majounie, E. Kalimo, H. Paetau, A. Abramzon, Y. Remes, A. Kaganovich, A. Scholz, S. Duckworth, J. Ding, J. Harmer, D. Hernandez, D.G. Waite, A. Johnson, J. Mok, K. Ryten, M. Trabzuni, D. Guerreiro, R. Orrell, R. Neal, J. Murray, A. Pearson, J. Jansen, I. Simón-Sánchez, J. Sondervan, D. Seelaar, H. Blake, D. Young, K. Halliwell, N. Callister, J. Toulson, G. Richardson, A. Gerhard, A. Snowden, J. Rollinson, S. Mann, D. Neary, D. Nalls, M.A. Peuralinna, T. Jansson, L. Isoviita, V.-M. Kaivorinne, A.-L. Hölttä-Vuori, M. Ikonen, E. Sulkava, R. Gibbs, J. Benatar, M. Wuu, J. Chiò, A. Restagno, G. Borghero, G. Sabatelli, M. Heckerman, D. Rogaeva, E. Zinman, L. Rothstein, J. Schymick, J. Sendtner, M. Drepper, C. Eichler, E. Alkan, C. Abdullaev, Z. Pack, S. Dutra, A. Pak, E. Hardy, J. Singleton, A. Laaksovirta, H. Williams, N. Heutink, P. Pickering-Brown, S. Morris, H. Tienari, P.J. Traynor, B. Swieten, J.C. van Myllykangas, L. |
2011-10-20
|
|
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
(Article)
Rascovsky, K. Hodges, J. Hillis, A.E. Josephs, K.A. Boeve, B.F. Kertesz, A. Seeley, W.W. Rankin, K.P. Johnson, J.K. Gorno-Tempini, M.-L. Rosen, H. Prioleau-Latham, C.E. Knopman, D.S. Lee, A. Kipps, C.M. Lillo, P. Piguet, O. Rohrer, J.D. Rossor, M. Warren, J.D. Fox, N.C. Galasko, D. Salmon, D.P. Mendez, M.F. Black, S.E. Mesulam, M. Weintraub, S. Dickerson, B.C. Diehl-Schmid, J. Pasquier, F. Deramecourt, V. Lebert, F. Pijnenburg, Y. Chow, T.W. Kramer, J.H. Manes, F. Grafman, J. Cappa, S.F. Freedman, M. Grossman, M. Miller, B.L. Neuhaus, J. Swieten, J.C. van Seelaar, H. Dopper, E.G.P. Onyike, C.U. |
2011-09-01
|
|
Brain perfusion patterns in familial frontotemporal lobar degeneration
(Article)
Seelaar, H. Papma, J.M. Garraux, G. Koning, I. de Reijs, A.E.M. Valkema, R. Rozemuller, A.J.M. Salmon, E. Swieten, J.C. van |
2011-07-26
|
|
Clinical, genetic and pathological heterogeneity of frontotemporal dementia: A review
(Article)
Seelaar, H. Rohrer, J.D. Pijnenburg, Y. Fox, N.C. Swieten, J.C. van |
2011-05-01
|
|
Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders
(Article)
Hortobágyi, T. Troakes, C. Nishimura, A.L. Vance, C. Swieten, J.C. van Seelaar, H. King, A.A. Al-Sarraj, S. Rogelj, B. Shaw, C.E. |
2011-04-01
|
|
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
|
|
Frontotemporal Dementia: clinical, genetic, and pathological heterogeneity
(Doctoral Thesis)
Seelaar, H. |
2011-03-23
|
|
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
|
|
Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration
(Article)
Seelaar, H. Klijnsma, K.Y. Koning, I. de Lugt, A. van der Chiu, W.Z. Azmani, A. Rozemuller, A.J.M. Swieten, J.C. van |
2010-05-01
|
