-
1
-
-
0034904509
-
Recent advances in the understanding of tau protein and movement disorders
-
Arvanitakis Z, Wszolek ZK. Recent advances in the understanding of tau protein and movement disorders. Curr Opin Neurol 2001; 14: 491-7.
-
(2001)
Curr Opin Neurol
, vol.14
, pp. 491-497
-
-
Arvanitakis, Z.1
Wszolek, Z.K.2
-
2
-
-
0037327535
-
Tau phosphorylation and kinase activation in familial tauopathy linked to deln296 mutation
-
Ferrer I, Pastor P, Rey MJ, Munoz E, Puig B, Pastor E, et al. Tau phosphorylation and kinase activation in familial tauopathy linked to deln296 mutation. Neuropathol Appl Neurobiol 2003; 29: 23-34.
-
(2003)
Neuropathol Appl Neurobiol
, vol.29
, pp. 23-34
-
-
Ferrer, I.1
Pastor, P.2
Rey, M.J.3
Munoz, E.4
Puig, B.5
Pastor, E.6
-
3
-
-
19944428327
-
Pick bodies in a family with presenilin-1 Alzheimer's disease
-
Halliday GM, Song YJC, Lepar G, Brooks WS, Kwok JB, Kersaitis C, et al. Pick bodies in a family with presenilin-1 Alzheimer's disease. Ann Neurol 2005; 57: 139-43.
-
(2005)
Ann Neurol
, vol.57
, pp. 139-143
-
-
Halliday, G.M.1
Song, Y.J.C.2
Lepar, G.3
Brooks, W.S.4
Kwok, J.B.5
Kersaitis, C.6
-
4
-
-
0034877085
-
Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and widespread tau accumulation in the glial cells
-
Iseki E, Matsumura T, Marui W, Hino H, Odawara T, Sugiyama N, et al. Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and widespread tau accumulation in the glial cells. Acta Neuropathol 2001; 102: 285-92.
-
(2001)
Acta Neuropathol
, vol.102
, pp. 285-292
-
-
Iseki, E.1
Matsumura, T.2
Marui, W.3
Hino, H.4
Odawara, T.5
Sugiyama, N.6
-
5
-
-
0038796582
-
Frontotemporal dementia and parkinsonism with P301S tau gene mutation in a Jewish family
-
Lossos A, Reches A, Gal A, Newman JP, Soffer D, Gomori JM, et al. Frontotemporal dementia and parkinsonism with P301S tau gene mutation in a Jewish family. J Neurol 2003; 250: 733-40.
-
(2003)
J Neurol
, vol.250
, pp. 733-740
-
-
Lossos, A.1
Reches, A.2
Gal, A.3
Newman, J.P.4
Soffer, D.5
Gomori, J.M.6
-
6
-
-
0035134195
-
Familial atypical progressive supranuclear palsy associated with homozygosity for the delN296 mutation in the tau gene
-
Pastor P, Pastor E, Carnero C, Vela R, Garcia T, Amer G, et al. Familial atypical progressive supranuclear palsy associated with homozygosity for the delN296 mutation in the tau gene. Ann Neurol 2001; 49: 263-67.
-
(2001)
Ann Neurol
, vol.49
, pp. 263-267
-
-
Pastor, P.1
Pastor, E.2
Carnero, C.3
Vela, R.4
Garcia, T.5
Amer, G.6
-
7
-
-
0036316037
-
Progressive supranuclear palsy: Clinical and genetic aspects
-
Pastor P, Tolosa E. Progressive supranuclear palsy: clinical and genetic aspects. Curr Opin Neurol 2002; 15: 429-37.
-
(2002)
Curr Opin Neurol
, vol.15
, pp. 429-437
-
-
Pastor, P.1
Tolosa, E.2
-
8
-
-
0036771837
-
An R5L tau mutation in a subject with progressive supranuclear palsy phenotype
-
Poorkaj P, Muma NA, Zhukareva V, Cochran EJ, Shannon KM, Hurtig H, et al. An R5L tau mutation in a subject with progressive supranuclear palsy phenotype. Ann Neurol 2002; 52: 511-6.
-
(2002)
Ann Neurol
, vol.52
, pp. 511-516
-
-
Poorkaj, P.1
Muma, N.A.2
Zhukareva, V.3
Cochran, E.J.4
Shannon, K.M.5
Hurtig, H.6
-
10
-
-
0034051721
-
Tau mutations in familial frontotemporal dementia
-
Spillantini MG, Goedert M. Tau mutations in familial frontotemporal dementia. [Editorial]. Brain 2000; 123: 857-9.
-
(2000)
Brain
, vol.123
, pp. 857-859
-
-
Spillantini, M.G.1
Goedert, M.2
-
11
-
-
0034093228
-
Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene. Expansion of the disease phenotype caused by tau gene mutations
-
Stanford PM, Halliday GM, Brooks WS, Kwok JBJ, Storey CE, Creasey H, et al. Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene. Expansion of the disease phenotype caused by tau gene mutations. Brain 2000; 123: 880-93.
-
(2000)
Brain
, vol.123
, pp. 880-893
-
-
Stanford, P.M.1
Halliday, G.M.2
Brooks, W.S.3
Kwok, J.B.J.4
Storey, C.E.5
Creasey, H.6
-
12
-
-
33244488121
-
Progressive supranuclear palsy, frontotemporal dementia with parkinsonism linked to chromosome 17 and familial tauopathies
-
Stanford PM, Halliday GM, Brooks WS, Kwok JBJ, Schofield PR. Progressive supranuclear palsy, frontotemporal dementia with parkinsonism linked to chromosome 17 and familial tauopathies [reply]. Brain 2001; 124: 1668-70.
-
(2001)
Brain
, vol.124
, pp. 1668-1670
-
-
Stanford, P.M.1
Halliday, G.M.2
Brooks, W.S.3
Kwok, J.B.J.4
Schofield, P.R.5
-
13
-
-
0242317909
-
Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia
-
Stanford PM, Shepherd CE, Halliday GM, Brooks WS, Schofield PW, Brodaty H, et al. Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia. Brain 2003; 126: 814-26.
-
(2003)
Brain
, vol.126
, pp. 814-826
-
-
Stanford, P.M.1
Shepherd, C.E.2
Halliday, G.M.3
Brooks, W.S.4
Schofield, P.W.5
Brodaty, H.6
-
14
-
-
0034907406
-
Progressive supranuclear palsy as a disease phenotype caused by S305S tau gene mutation
-
Wszolek ZK, Tsuboi Y, Uitti RJ, Reed L, Hutton ML, Dickson DW. Progressive supranuclear palsy as a disease phenotype caused by S305S tau gene mutation [letter]. Brain 2001; 124: 1666-8.
-
(2001)
Brain
, vol.124
, pp. 1666-1668
-
-
Wszolek, Z.K.1
Tsuboi, Y.2
Uitti, R.J.3
Reed, L.4
Hutton, M.L.5
Dickson, D.W.6
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