-
1
-
-
8944226575
-
Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): Report of the NINDS-SPSP International Workshop
-
Litvan I, Agid Y, Calne D, et al. Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP International Workshop. Neurology. 1996;47:1-9.
-
(1996)
Neurology
, vol.47
, pp. 1-9
-
-
Litvan, I.1
Agid, Y.2
Calne, D.3
-
2
-
-
0029854681
-
Neuropsychiatric aspects of progressive supranuclear palsy
-
Litvan I, Mega MS, Cummings JL, Fairbanks L. Neuropsychiatric aspects of progressive supranuclear palsy. Neurology. 1996;47:1184-1189.
-
(1996)
Neurology
, vol.47
, pp. 1184-1189
-
-
Litvan, I.1
Mega, M.S.2
Cummings, J.L.3
Fairbanks, L.4
-
3
-
-
0029349321
-
Neuropsychological features of progressive supranuclear palsy
-
Grafman J, Litvan I, Stark M. Neuropsychological features of progressive supranuclear palsy. Brain Cogn. 1995;28:311-320.
-
(1995)
Brain Cogn
, vol.28
, pp. 311-320
-
-
Grafman, J.1
Litvan, I.2
Stark, M.3
-
4
-
-
0028092015
-
Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy)
-
Hauw JUJU, Daniel SE, Dickson D, et al. Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy). Neurology. 1994;44:2015-2019.
-
(1994)
Neurology
, vol.44
, pp. 2015-2019
-
-
Hauw, J.U.J.U.1
Daniel, S.E.2
Dickson, D.3
-
5
-
-
0028183597
-
The neuropathology of progressive supranuclear palsy
-
Lantos PL. The neuropathology of progressive supranuclear palsy. J Neural Transm. 1994;42(suppl):137-152.
-
(1994)
J Neural Transm
, vol.42
, Issue.SUPPL.
, pp. 137-152
-
-
Lantos, P.L.1
-
6
-
-
0032833626
-
Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration
-
Dickson DW. Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration. J Neurol. 1999;246(suppl 2):6-15.
-
(1999)
J Neurol
, vol.246
, Issue.SUPPL. 2
, pp. 6-15
-
-
Dickson, D.W.1
-
7
-
-
0032784539
-
Clinical genetics of familial progressive supranuclear palsy
-
Rojo A, Pernaute RS, Fontan A, et al. Clinical genetics of familial progressive supranuclear palsy. Brain. 1999;122:1233-1245.
-
(1999)
Brain
, vol.122
, pp. 1233-1245
-
-
Rojo, A.1
Pernaute, R.S.2
Fontan, A.3
-
8
-
-
0034904509
-
Recent advances in understanding of tau protein and movement disorders
-
Arvanitakis Z, Wszolek ZK. Recent advances in understanding of tau protein and movement disorders. Curr Opin Neurol. 2001;14:491-497.
-
(2001)
Curr Opin Neurol
, vol.14
, pp. 491-497
-
-
Arvanitakis, Z.1
Wszolek, Z.K.2
-
9
-
-
0032573083
-
Pathogenic implications of mutation in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
-
Clark LN, Poorkaj P, Wszolek ZK, et al. Pathogenic implications of mutation in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17. Proc Natl Acad Sci U S A. 1998;95:13103-13107.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 13103-13107
-
-
Clark, L.N.1
Poorkaj, P.2
Wszolek, Z.K.3
-
10
-
-
0033002879
-
A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a taupathy with dementia and supranuclear palsy
-
Delisle MB, Murrell JR, Richardson R, et al. A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a taupathy with dementia and supranuclear palsy. Acta Neuropathol. 1999;98:62-77.
-
(1999)
Acta Neuropathol
, vol.98
, pp. 62-77
-
-
Delisle, M.B.1
Murrell, J.R.2
Richardson, R.3
-
11
-
-
0033546987
-
A mutation in the microtubule-associated tau protein in pallido-nigro-luysian degeneration
-
Yasuda M, Kawamata T, Komure O, et al. A mutation in the microtubule-associated tau protein in pallido-nigro-luysian degeneration. Neurology. 1999;53:864-868.
-
(1999)
Neurology
, vol.53
, pp. 864-868
-
-
Yasuda, M.1
Kawamata, T.2
Komure, O.3
-
12
-
-
0034624917
-
Two brothers with fronto-temporal dementia and parkinsonism with an N279K mutation of the tau gene
-
Arima K, Kowalska A, Hasegawa M, et al. Two brothers with fronto-temporal dementia and parkinsonism with an N279K mutation of the tau gene. Neurology. 2000;54:1787-1795.
-
(2000)
Neurology
, vol.54
, pp. 1787-1795
-
-
Arima, K.1
Kowalska, A.2
Hasegawa, M.3
-
13
-
-
84982538792
-
MRI in corticobasal degeneration
-
Grisoli M, Fetoni V, Savoiardo M, Girotti F, Bruzzone MG. MRI in corticobasal degeneration. Eur J Neurol. 1994;2:547-552.
-
(1994)
Eur J Neurol
, vol.2
, pp. 547-552
-
-
Grisoli, M.1
Fetoni, V.2
Savoiardo, M.3
Girotti, F.4
Bruzzone, M.G.5
-
14
-
-
0028183596
-
PET studies in progressive supranuclear palsy
-
Brooks DJ. PET studies in progressive supranuclear palsy. J Neural Transm. 1994;42(suppl):119-134.
-
(1994)
J Neural Transm
, vol.42
, Issue.SUPPL.
, pp. 119-134
-
-
Brooks, D.J.1
-
15
-
-
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 mutation
-
Stanford PM, Halliday GM, Brooks WS, 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 mutation. Brain. 2000;123:880-893.
-
(2000)
Brain
, vol.123
, pp. 880-893
-
-
Stanford, P.M.1
Halliday, G.M.2
Brooks, W.S.3
-
16
-
-
0035412946
-
Fronto-temporal dementia and parkinsonism linked to chromosome (17 FTDP-17): PPND family: A longitudinal videotape demonstration
-
Wszolek ZK, Kardon RH, Wolters EC, et al. Fronto-temporal dementia and parkinsonism linked to chromosome (17 FTDP-17): PPND family: a longitudinal videotape demonstration. Mov Disord. 2001;16:756-760.
-
(2001)
Mov Disord
, vol.16
, pp. 756-760
-
-
Wszolek, Z.K.1
Kardon, R.H.2
Wolters, E.C.3
-
17
-
-
0034705093
-
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration
-
Wszolek ZK, Uitti RJ, Hutton M. A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration [letter]. Neurology. 2000;54:2028-2030.
-
(2000)
Neurology
, vol.54
, pp. 2028-2030
-
-
Wszolek, Z.K.1
Uitti, R.J.2
Hutton, M.3
-
18
-
-
0036279601
-
Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: A comparison of the pallido-ponto-nigral degeneration kindred and a French family
-
Tsubol Y, Uitti RJ, Delisle MB, et al. Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallido-ponto-nigral degeneration kindred and a French family. Arch Neurol. 2002;59:943-950.
-
(2002)
Arch Neurol
, vol.59
, pp. 943-950
-
-
Tsubol, Y.1
Uitti, R.J.2
Delisle, M.B.3
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