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Spillantini, M.G.

( M.G. Spillantini)


patient inclusion family frontotemporal dementia brain dementia frontotemporal mutation tau gene chromosome disease ubiquitin-positive region atrophy cortex linkage analysis neurone study motor neurone disease tau mutations protein marker antibody onset family members spillantini tau-negative inclusions heutink neurol score swieten symptom memory van swieten jc cytoplasmic ubiquitin-positive inclusions parkinsonism ftd cases entorhinal cortex member feature tau protein layer dentate gyrus isoform ftd families 2 receptors presence acta neuropathol tau-negative nucleus hyperorality motor -17 staining rizzu p van swieten speech p 301s mutation ubiquitin pathology evidence lewy bodies problem cytoplasmic murrell jr neurofibrillary tangles tau pathology ftdp -17 tau-related ftd netherland netherlands brain bank rosso stevens m striatal dopamine ubiquitin inclusions lod scores pcr products kovari kertesz




3 Most Recent Publications

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions (Article)
Deerlin, V.M. Sleiman, P.M.A. Arnold, S.E. Mann, D. Pickering-Brown, S. Seelaar, H. Heutink, P. Swieten, J.C. van Murrell, J.R. Ghetti, B. Spina, S. Grafman, J. Martinez-Lage, M. Hodges, J. Spillantini, M.G. Gilman, S. Lieberman, A.P. Kaye, J.A. Woltjer, R.L. Bigio, E.H. Mesulam, M. Al-Sarraj, S. Troakes, C. Chen-Plotkin, A. Rosenberg, R.N. White, C.L. Ferrer, I. Lladó, A. Neumann, H.A.M. Kretzschmar, H.A. Hulette, C. Welsh-Bohmer, K.A. Miller, B.L. Alzualde, A. Wang, L. Munain, A.L. de McKee, A.C. Gearing, M. Levey, A.I. Lah, J.J. Hardy, J. Rohrer, J.D. Lashley, T. Mackenzie, I.R.A. Feldman, H.H. Graff-Radford, N.R. Hamilton, R.L. Dekosky, S.T. Zee, J. van der Kumar-Singh, S. Broeckhoven, C. van Mayeux, R. Vonsattel, J.P. Troncoso, J.C. Kril, J.J. Kwok, J.B.J. Dickson, D. Halliday, G.M. Bird, T.D. Ince, P.G. Shaw, P.J. Cairns, N.J. Morris, J.C. McLean, C.A. DeCarli, C. Ellis, W.G. Freeman, S.H. Rademakers, R. Frosch, M.P. Growdon, J.H. Perl, D.P. Sano, M. Bennett, D.A. Schneider, J.A. Beach, T.G. Reiman, E.M. Woodruff, B.K. Cummings, J.F. Boeve, B. Vinters, H.V. Miller, C.A. Chui, H. Alafuzoff, I. Hartikainen, P. Seilhean, D. Galasko, D. Masliah, E. Cotman, C.W. Tũón, M.T. Grossman, M. Martínez, M.C.C. Munoz, D.G. Carroll, S.L. Marson, D. Riederer, P.F. Bogdanovic, N. Schellenberg, G.D. Hakonarson, H. Trojanowski, J.Q. Lee, V.M.Y.
2010-03-01
Hereditary frontotemporal dementia caused by Tau gene mutations (Article)
Swieten, J.C. van Spillantini, M.G.
2007-01-01
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22 (Article)
Rosso, S.M. Kamphorst, W. Graaf, B.M. de Willemsen, R. Ravid, R. Niermeijer, M.F. Spillantini, M.G. Heutink, P.
2001-01-01