-
1
-
-
75549116708
-
Progressive supranuclear palsy. A heterogeneous degeneration involving the brain stem, basal ganglia and cerebellum with vertical gaze and pseudobulbar palsy, nuchal dystonia and dementia
-
J.C. Steele, J.C. Richardson, and J. Olszewski Progressive supranuclear palsy. A heterogeneous degeneration involving the brain stem, basal ganglia and cerebellum with vertical gaze and pseudobulbar palsy, nuchal dystonia and dementia Arch Neurol 10 1964 333 359
-
(1964)
Arch Neurol
, vol.10
, pp. 333-359
-
-
Steele, J.C.1
Richardson, J.C.2
Olszewski, J.3
-
2
-
-
0028092015
-
Preliminary NINDS neuropathologic criteria for Steele-Richardson- Olszewski syndrome (progressive supranuclear palsy)
-
J.J. Hauw, S.E. Daniel, D. Dickson, D.S. Horoupian, K. Jellinger, and P.L. Lantos Preliminary NINDS neuropathologic criteria for Steele-Richardson- Olszewski syndrome (progressive supranuclear palsy) Neurology 44 1994 2015 2019
-
(1994)
Neurology
, vol.44
, pp. 2015-2019
-
-
Hauw, J.J.1
Daniel, S.E.2
Dickson, D.3
Horoupian, D.S.4
Jellinger, K.5
Lantos, P.L.6
-
3
-
-
0035146717
-
Distinct isoforms of tau aggregated in neurons and glial cells in brains of patients with Pick's disease, corticobasal degeneration and progressive supranuclear palsy
-
T. Arai, K. Ikeda, H. Akiyama, Y. Shikamoto, K. Tsuchiya, and S. Yagishita Distinct isoforms of tau aggregated in neurons and glial cells in brains of patients with Pick's disease, corticobasal degeneration and progressive supranuclear palsy Acta Neuropathol 101 2001 167 173
-
(2001)
Acta Neuropathol
, vol.101
, pp. 167-173
-
-
Arai, T.1
Ikeda, K.2
Akiyama, H.3
Shikamoto, Y.4
Tsuchiya, K.5
Yagishita, S.6
-
4
-
-
77954604622
-
Neuropathology of variants of progressive supranuclear palsy
-
D.W. Dickson, Z. Ahmed, A.A. Algom, Y. Tsuboi, and K.A. Josephs Neuropathology of variants of progressive supranuclear palsy Curr Opin Neurol 23 2010 394 400
-
(2010)
Curr Opin Neurol
, vol.23
, pp. 394-400
-
-
Dickson, D.W.1
Ahmed, Z.2
Algom, A.A.3
Tsuboi, Y.4
Josephs, K.A.5
-
5
-
-
34250865548
-
Pathological tau burden and distribution distinguishes progressive supranuclear palsy-parkinsonism from Richardson's syndrome
-
D.R. Williams, J.L. Holton, C. Strand, A. Pittman, R. de Silva, and A.J. Lees Pathological tau burden and distribution distinguishes progressive supranuclear palsy-parkinsonism from Richardson's syndrome Brain 130 2007 1566 1576
-
(2007)
Brain
, vol.130
, pp. 1566-1576
-
-
Williams, D.R.1
Holton, J.L.2
Strand, C.3
Pittman, A.4
De Silva, R.5
Lees, A.J.6
-
6
-
-
60249088182
-
Progressive supranuclear palsy: Clinicopathological concepts and diagnostic challenges
-
D.R. Williams, and A.J. Lees Progressive supranuclear palsy: clinicopathological concepts and diagnostic challenges Lancet Neurol 8 2009 270 279
-
(2009)
Lancet Neurol
, vol.8
, pp. 270-279
-
-
Williams, D.R.1
Lees, A.J.2
-
7
-
-
0030862210
-
Cortical degeneration in progressive supranuclear palsy. A comparison with cortical-basal ganglionic degeneration
-
C. Bergeron, M.S. Pollanen, L. Weyer, and A.E. Lang Cortical degeneration in progressive supranuclear palsy. A comparison with cortical-basal ganglionic degeneration J Neuropathol Exp Neurol 56 1997 726 734
-
(1997)
J Neuropathol Exp Neurol
, vol.56
, pp. 726-734
-
-
Bergeron, C.1
Pollanen, M.S.2
Weyer, L.3
Lang, A.E.4
-
8
-
-
0034999577
-
Cortical synapse loss in progressive supranuclear palsy
-
E.H. Bigio, M.B. Vono, S. Satumtira, J. Adamson, E. Sontag, and L.S. Hynan Cortical synapse loss in progressive supranuclear palsy J Neuropathol Exp Neurol 60 2001 403 410
-
(2001)
J Neuropathol Exp Neurol
, vol.60
, pp. 403-410
-
-
Bigio, E.H.1
Vono, M.B.2
Satumtira, S.3
Adamson, J.4
Sontag, E.5
Hynan, L.S.6
-
9
-
-
0036942725
-
Progressive supranuclear palsy with asymmetric tau pathology presenting with unilateral limb dystonia
-
T. Oide, S. Ohara, M. Yazawa, K. Inoue, N. Itoh, and T. Tokuda Progressive supranuclear palsy with asymmetric tau pathology presenting with unilateral limb dystonia Acta Neuropathol 104 2002 209 214
-
(2002)
Acta Neuropathol
, vol.104
, pp. 209-214
-
-
Oide, T.1
Ohara, S.2
Yazawa, M.3
Inoue, K.4
Itoh, N.5
Tokuda, T.6
-
10
-
-
26444469061
-
Increased tau burden in the cortices of progressive supranuclear palsy presenting with corticobasal syndrome
-
Y. Tsuboi, K.A. Josephs, B.F. Boeve, I. Litvan, R.J. Caselli, and J.N. Caviness Increased tau burden in the cortices of progressive supranuclear palsy presenting with corticobasal syndrome Mov Disord 20 2005 982 988
-
(2005)
Mov Disord
, vol.20
, pp. 982-988
-
-
Tsuboi, Y.1
Josephs, K.A.2
Boeve, B.F.3
Litvan, I.4
Caselli, R.J.5
Caviness, J.N.6
-
11
-
-
0000443399
-
Über einen wenig bekannten spinalen Symptomenkomplex
-
W.H. Erb Über einen wenig bekannten spinalen Symptomenkomplex Klin Wochenschr 12 1875 357 359
-
(1875)
Klin Wochenschr
, vol.12
, pp. 357-359
-
-
Erb, W.H.1
-
12
-
-
0026682621
-
Primary lateral sclerosis. Clinical features, neuropathology and diagnostic criteria
-
C.E. Pringle, A.J. Hudson, D.G. Munoz, J.A. Kiernan, W.F. Brown, and G.C. Ebers Primary lateral sclerosis. Clinical features, neuropathology and diagnostic criteria Brain 115 1992 495 520
-
(1992)
Brain
, vol.115
, pp. 495-520
-
-
Pringle, C.E.1
Hudson, A.J.2
Munoz, D.G.3
Kiernan, J.A.4
Brown, W.F.5
Ebers, G.C.6
-
13
-
-
0031666851
-
Upper motor neuron predominant degeneration with frontal and temporal lobe atrophy
-
M. Konagaya, M. Sakai, Y. Matsuoka, Y. Konagaya, and Y. Hashizume Upper motor neuron predominant degeneration with frontal and temporal lobe atrophy Acta Neuropathol 96 1998 532 536
-
(1998)
Acta Neuropathol
, vol.96
, pp. 532-536
-
-
Konagaya, M.1
Sakai, M.2
Matsuoka, Y.3
Konagaya, Y.4
Hashizume, Y.5
-
14
-
-
0030704626
-
Primary lateral sclerosis
-
R. Watanabe, M. Iino, M. Honda, J. Sano, and M. Hara Primary lateral sclerosis Neuropathology 17 1997 220 224
-
(1997)
Neuropathology
, vol.17
, pp. 220-224
-
-
Watanabe, R.1
Iino, M.2
Honda, M.3
Sano, J.4
Hara, M.5
-
16
-
-
0029036659
-
A 65-year-old woman with dysarthria, dysphagia, weakness, and gait disturbance
-
H. Imai, Y. Furukawa, S. Sumino, H. Mori, G. Ueda, and T. Shirai A 65-year-old woman with dysarthria, dysphagia, weakness, and gait disturbance No To Shinkei 47 1995 399 410
-
(1995)
No to Shinkei
, vol.47
, pp. 399-410
-
-
Imai, H.1
Furukawa, Y.2
Sumino, S.3
Mori, H.4
Ueda, G.5
Shirai, T.6
-
17
-
-
84864132237
-
Primary lateral sclerosis: Upper-motor-predominant amyotrophic lateral sclerosis with frontotemporal lobar degeneration - Immunohistochemical and biochemical analyses of TDP-43
-
T. Kosaka, Y.J. Fu, A. Shiga, H. Ishidaira, C.F. Tan, and T. Tani Primary lateral sclerosis: upper-motor-predominant amyotrophic lateral sclerosis with frontotemporal lobar degeneration - immunohistochemical and biochemical analyses of TDP-43 Neuropathology 32 2012 373 384
-
(2012)
Neuropathology
, vol.32
, pp. 373-384
-
-
Kosaka, T.1
Fu, Y.J.2
Shiga, A.3
Ishidaira, H.4
Tan, C.F.5
Tani, T.6
-
18
-
-
0023823645
-
Ubiquitin deposits in anterior horn cells in motor neurone disease
-
P.N. Leigh, B.H. Anderton, A. Dodson, J.M. Gallo, M. Swash, and D.M. Power Ubiquitin deposits in anterior horn cells in motor neurone disease Neurosci Lett 93 1988 197 203
-
(1988)
Neurosci Lett
, vol.93
, pp. 197-203
-
-
Leigh, P.N.1
Anderton, B.H.2
Dodson, A.3
Gallo, J.M.4
Swash, M.5
Power, D.M.6
-
19
-
-
0033033277
-
Sporadic amyotrophic lateral sclerosis resembling primary lateral sclerosis: Report of an autopsy case and a review of the literature
-
K. Tsuchiya, M. Arai, S. Matsuya, H. Nishimura, T. Ishiko, and H. Kondo Sporadic amyotrophic lateral sclerosis resembling primary lateral sclerosis: report of an autopsy case and a review of the literature Neuropathology 19 1999 71 76
-
(1999)
Neuropathology
, vol.19
, pp. 71-76
-
-
Tsuchiya, K.1
Arai, M.2
Matsuya, S.3
Nishimura, H.4
Ishiko, T.5
Kondo, H.6
-
20
-
-
0017758030
-
Pure spastic paralysis of corticospinal origin
-
C.M. Fisher Pure spastic paralysis of corticospinal origin Can J Neurol Sci 4 1977 251 258
-
(1977)
Can J Neurol Sci
, vol.4
, pp. 251-258
-
-
Fisher, C.M.1
-
21
-
-
0019465385
-
Primary lateral sclerosis: A case report
-
M.F. Beal, and E.P. Richardson Jr. Primary lateral sclerosis: a case report Arch Neurol 38 1981 630 633
-
(1981)
Arch Neurol
, vol.38
, pp. 630-633
-
-
Beal, M.F.1
Richardson Jr., E.P.2
-
22
-
-
0023796160
-
Primary lateral sclerosis. A clinical diagnosis reemerges
-
D.S. Younger, S. Chou, A.P. Hays, D.J. Lange, R. Emerson, and M. Brin Primary lateral sclerosis. A clinical diagnosis reemerges Arch Neurol 45 1988 1304 1307
-
(1988)
Arch Neurol
, vol.45
, pp. 1304-1307
-
-
Younger, D.S.1
Chou, S.2
Hays, A.P.3
Lange, D.J.4
Emerson, R.5
Brin, M.6
-
23
-
-
0038170494
-
Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies
-
R. de Silva, T. Lashley, G. Gibb, D. Hanger, A. Hope, and A. Reid Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies Neuropathol Appl Neurobiol 29 2003 288 302
-
(2003)
Neuropathol Appl Neurobiol
, vol.29
, pp. 288-302
-
-
De Silva, R.1
Lashley, T.2
Gibb, G.3
Hanger, D.4
Hope, A.5
Reid, A.6
-
24
-
-
65649144764
-
Clinicopathological characterization of Pick's disease versus frontotemporal lobar degeneration with ubiquitin/TDP-43-positive inclusions
-
O. Yokota, K. Tsuchiya, T. Arai, S. Yagishita, O. Matsubara, and A. Mochizuki Clinicopathological characterization of Pick's disease versus frontotemporal lobar degeneration with ubiquitin/TDP-43-positive inclusions Acta Neuropathol 117 2009 429 444
-
(2009)
Acta Neuropathol
, vol.117
, pp. 429-444
-
-
Yokota, O.1
Tsuchiya, K.2
Arai, T.3
Yagishita, S.4
Matsubara, O.5
Mochizuki, A.6
-
25
-
-
4444347376
-
Staging of argyrophilic grains: An age-associated tauopathy
-
Y. Saito, N.N. Ruberu, M. Sawabe, T. Arai, N. Tanaka, and Y. Kakuta Staging of argyrophilic grains: an age-associated tauopathy J Neuropathol Exp Neurol 63 2004 911 918
-
(2004)
J Neuropathol Exp Neurol
, vol.63
, pp. 911-918
-
-
Saito, Y.1
Ruberu, N.N.2
Sawabe, M.3
Arai, T.4
Tanaka, N.5
Kakuta, Y.6
-
26
-
-
0030803611
-
Argyrophilic grain disease: Distribution of grains in patients with and without dementia
-
M. Tolnay, M. Schwietert, A.U. Monsch, H.B. Staehelin, D. Langui, and A. Probst Argyrophilic grain disease: distribution of grains in patients with and without dementia Acta Neuropathol 94 1997 353 358
-
(1997)
Acta Neuropathol
, vol.94
, pp. 353-358
-
-
Tolnay, M.1
Schwietert, M.2
Monsch, A.U.3
Staehelin, H.B.4
Langui, D.5
Probst, A.6
-
27
-
-
54449096081
-
White matter tauopathy with globular glial inclusions: A distinct sporadic frontotemporal lobar degeneration
-
G.G. Kovacs, K. Majtenyi, S. Spina, J.R. Murrell, E. Gelpi, and R. Hoftberger White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration J Neuropathol Exp Neurol 67 2008 963 975
-
(2008)
J Neuropathol Exp Neurol
, vol.67
, pp. 963-975
-
-
Kovacs, G.G.1
Majtenyi, K.2
Spina, S.3
Murrell, J.R.4
Gelpi, E.5
Hoftberger, R.6
-
28
-
-
56749083283
-
Apraxia of speech and nonfluent aphasia: A new clinical marker for corticobasal degeneration and progressive supranuclear palsy
-
K.A. Josephs, and J.R. Duffy Apraxia of speech and nonfluent aphasia: a new clinical marker for corticobasal degeneration and progressive supranuclear palsy Curr Opin Neurol 21 2008 688 692
-
(2008)
Curr Opin Neurol
, vol.21
, pp. 688-692
-
-
Josephs, K.A.1
Duffy, J.R.2
-
29
-
-
33745007339
-
Atypical progressive supranuclear palsy with corticospinal tract degeneration
-
K.A. Josephs, O. Katsuse, D.A. Beccano-Kelly, W.L. Lin, R.J. Uitti, and Y. Fujino Atypical progressive supranuclear palsy with corticospinal tract degeneration J Neuropathol Exp Neurol 65 2006 396 405
-
(2006)
J Neuropathol Exp Neurol
, vol.65
, pp. 396-405
-
-
Josephs, K.A.1
Katsuse, O.2
Beccano-Kelly, D.A.3
Lin, W.L.4
Uitti, R.J.5
Fujino, Y.6
-
31
-
-
0034792793
-
Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature
-
N. Le Forestier, T. Maisonobe, A. Piquard, S. Rivaud, L. Crevier-Buchman, and F. Salachas Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature Brain 124 2001 1989 1999
-
(2001)
Brain
, vol.124
, pp. 1989-1999
-
-
Le Forestier, N.1
Maisonobe, T.2
Piquard, A.3
Rivaud, S.4
Crevier-Buchman, L.5
Salachas, F.6
-
32
-
-
84885973796
-
Progressive supranuclear palsy and corticobasal degeneration
-
D.W. Dickson, R.O. Weller, 2nd edn Wiley-Blackwell
-
D.W. Dickson, J.J. Hauw, Y. Agid, and I. Litvan Progressive supranuclear palsy and corticobasal degeneration D.W. Dickson, R.O. Weller, Neurodegeneration: the molecular pathology of dementia and movement disorders 2nd edn 2011 Wiley-Blackwell 135 155
-
(2011)
Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders
, pp. 135-155
-
-
Dickson, D.W.1
Hauw, J.J.2
Agid, Y.3
Litvan, I.4
-
33
-
-
23844558327
-
Atypical progressive supranuclear palsy underlying progressive apraxia of speech and nonfluent aphasia
-
K.A. Josephs, B.F. Boeve, J.R. Duffy, G.E. Smith, D.S. Knopman, and J.E. Parisi Atypical progressive supranuclear palsy underlying progressive apraxia of speech and nonfluent aphasia Neurocase 11 2005 283 296
-
(2005)
Neurocase
, vol.11
, pp. 283-296
-
-
Josephs, K.A.1
Boeve, B.F.2
Duffy, J.R.3
Smith, G.E.4
Knopman, D.S.5
Parisi, J.E.6
-
34
-
-
0029877434
-
Progressive supranuclear palsy: A clinicopathological study of 21 cases
-
M. Verny, K.A. Jellinger, J.J. Hauw, C. Bancher, I. Litvan, and Y. Agid Progressive supranuclear palsy: a clinicopathological study of 21 cases Acta Neuropathol 91 1996 427 431
-
(1996)
Acta Neuropathol
, vol.91
, pp. 427-431
-
-
Verny, M.1
Jellinger, K.A.2
Hauw, J.J.3
Bancher, C.4
Litvan, I.5
Agid, Y.6
-
35
-
-
0029761242
-
The significance of cortical pathology in progressive supranuclear palsy. Clinico-pathological data in 10 cases
-
M. Verny, C. Duyckaerts, Y. Agid, and J.J. Hauw The significance of cortical pathology in progressive supranuclear palsy. Clinico-pathological data in 10 cases Brain 119 1996 1123 1136
-
(1996)
Brain
, vol.119
, pp. 1123-1136
-
-
Verny, M.1
Duyckaerts, C.2
Agid, Y.3
Hauw, J.J.4
-
36
-
-
20444436764
-
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism
-
D.R. Williams, R. de Silva, D.C. Paviour, A. Pittman, H.C. Watt, and L. Kilford Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism Brain 128 2005 1247 1258
-
(2005)
Brain
, vol.128
, pp. 1247-1258
-
-
Williams, D.R.1
De Silva, R.2
Paviour, D.C.3
Pittman, A.4
Watt, H.C.5
Kilford, L.6
-
37
-
-
77649138106
-
What features improve the accuracy of the clinical diagnosis of progressive supranuclear palsy-parkinsonism (PSP-P)?
-
D.R. Williams, and A.J. Lees What features improve the accuracy of the clinical diagnosis of progressive supranuclear palsy-parkinsonism (PSP-P)? Mov Disord 25 2010 357 362
-
(2010)
Mov Disord
, vol.25
, pp. 357-362
-
-
Williams, D.R.1
Lees, A.J.2
|