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Volumn 323, Issue 1-2, 2012, Pages 147-153

Progressive supranuclear palsy presenting as primary lateral sclerosis but lacking parkinsonism, gaze palsy, aphasia, or dementia

Author keywords

Motor neuron disease; Primary lateral sclerosis; Progressive supranuclear palsy; Pseudobulbar palsy; Pyramidal signs

Indexed keywords

TAU PROTEIN;

EID: 84867874064     PISSN: 0022510X     EISSN: 18785883     Source Type: Journal    
DOI: 10.1016/j.jns.2012.09.005     Document Type: Article
Times cited : (42)

References (37)
  • 1
    • 75549116708 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 5
    • 34250865548 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 9
    • 0036942725 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 15
    • 34447094657 scopus 로고    scopus 로고
    • TDP-43 in differential diagnosis of motor neuron disorders
    • D.W. Dickson, K.A. Josephs, and C. Amador-Ortiz TDP-43 in differential diagnosis of motor neuron disorders Acta Neuropathol 114 2007 71 79
    • (2007) Acta Neuropathol , vol.114 , pp. 71-79
    • Dickson, D.W.1    Josephs, K.A.2    Amador-Ortiz, C.3
  • 16
    • 0029036659 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 19
    • 0033033277 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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
  • 23
    • 0038170494 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 27
    • 54449096081 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 31
    • 0034792793 scopus 로고    scopus 로고
    • 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
  • 33
    • 23844558327 scopus 로고    scopus 로고
    • 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
  • 35
    • 0029761242 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.