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Volumn 22, Issue , 2016, Pages S34-S36

The phenotypic spectrum of progressive supranuclear palsy

Author keywords

Phenotypes; Progressive supranuclear palsy PSP; Tauopathy

Indexed keywords

ARTICLE; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; DISEASE DURATION; DISEASE SEVERITY; HUMAN; PHENOTYPE; PRIORITY JOURNAL; PROGRESSIVE SUPRANUCLEAR PALSY; PROGRESSIVE SUPRANUCLEAR PALSY WITH APRAXIA OF SPEECH; PROGRESSIVE SUPRANUCLEAR PALSY WITH CEREBELLAR ATAXIA; PROGRESSIVE SUPRANUCLEAR PALSY WITH CORTICOBASAL SYNDROME; PROGRESSIVE SUPRANUCLEAR PALSY WITH PREDOMINANT FRONTOTEMPORAL DYSFUNCTION; PROGRESSIVE SUPRANUCLEAR PALSY WITH PREDOMINANT PARKINSONISM; PROGRESSIVE SUPRANUCLEAR PALSY WITH PRIMARY LATERAL SCLEROSIS; PROGRESSIVE SUPRANUCLEAR PALSY WITH PROGRESSIVE NON FLUENT APHASIA; PROGRESSIVE SUPRANUCLEAR PALSY WITH PURE AKINESIA WITH GAIT FREEZING; PROGRESSIVE SUPRANUCLEAR PALSY WITH RICHARDSON SYNDROME; SENSITIVITY ANALYSIS; SYNDROME DELINEATION; ANIMAL; COMPLICATION; DIFFERENTIAL DIAGNOSIS; FALLING; GENETICS; PREVENTION AND CONTROL; SUPRANUCLEAR PALSY, PROGRESSIVE;

EID: 84947783804     PISSN: 13538020     EISSN: 18735126     Source Type: Journal    
DOI: 10.1016/j.parkreldis.2015.09.041     Document Type: Article
Times cited : (67)

References (30)
  • 1
    • 0034956738 scopus 로고    scopus 로고
    • The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UK
    • Nath U., Ben-Shlomo Y., Thomson R., Morris H.R., Wood N.W., Lees A.J., Burn D.J. The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UK. Brain 2001, 124:1438-1449.
    • (2001) Brain , vol.124 , pp. 1438-1449
    • Nath, U.1    Ben-Shlomo, Y.2    Thomson, R.3    Morris, H.R.4    Wood, N.W.5    Lees, A.J.6    Burn, D.J.7
  • 2
    • 0002450017 scopus 로고
    • Supranuclear ophthalmoplegia, pseudobulbar palsy, nuchal dystonia and dementia
    • Richardson J.C., Steele J.C., Olszewski J. Supranuclear ophthalmoplegia, pseudobulbar palsy, nuchal dystonia and dementia. Trans. Am. Neurol. Assoc. 1963, 8:25-29.
    • (1963) Trans. Am. Neurol. Assoc. , vol.8 , pp. 25-29
    • Richardson, J.C.1    Steele, J.C.2    Olszewski, J.3
  • 3
    • 20444436764 scopus 로고    scopus 로고
    • Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism
    • Williams D.R., de Silva R., Paviour D.C., Pittman A., Watt H.C., Kilford L., Holton J.L., Revesz T., Lees A.J. Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism. Brain 2005, 128:1247-1258.
    • (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    Holton, J.L.7    Revesz, T.8    Lees, A.J.9
  • 5
    • 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
    • Steele J.C., Richardson J.C., Olszewski J. 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. 1964, 10:333-359.
    • (1964) Arch. Neurol. , vol.10 , pp. 333-359
    • Steele, J.C.1    Richardson, J.C.2    Olszewski, J.3
  • 6
    • 0020568213 scopus 로고
    • Steele-Richardson-Olszewski disease without ophthalmoplegia. 6 clinico-anatomic cases
    • Dubas F., Gray F., Escourolle R. Steele-Richardson-Olszewski disease without ophthalmoplegia. 6 clinico-anatomic cases. Rev. Neurol. Paris 1983, 139:407-416.
    • (1983) Rev. Neurol. Paris , vol.139 , pp. 407-416
    • Dubas, F.1    Gray, F.2    Escourolle, R.3
  • 7
    • 0021879643 scopus 로고
    • Atypical presentation of progressive supranuclear palsy
    • Davis P.J., Bergeron C., McLachlan D.R. Atypical presentation of progressive supranuclear palsy. Ann. Neurol. 1985, 17:337-343.
    • (1985) Ann. Neurol. , vol.17 , pp. 337-343
    • Davis, P.J.1    Bergeron, C.2    McLachlan, D.R.3
  • 8
    • 60249088182 scopus 로고    scopus 로고
    • Progressive supranuclear palsy: clinico-pathological concepts and diagnostic challenges
    • Williams D.R., Lees A.J. Progressive supranuclear palsy: clinico-pathological concepts and diagnostic challenges. Lancet Neurol. 2009, 8:270-279.
    • (2009) Lancet Neurol. , vol.8 , pp. 270-279
    • Williams, D.R.1    Lees, A.J.2
  • 13
    • 77649138106 scopus 로고    scopus 로고
    • What features improve the accuracy of the clinical diagnosis of progressive supranuclear palsy-parkinsonism (PSP - P)?
    • Williams D.R., Lees A.J. What features improve the accuracy of the clinical diagnosis of progressive supranuclear palsy-parkinsonism (PSP - P)?. Mov. Disord. 2010, 25:357-362.
    • (2010) Mov. Disord. , vol.25 , pp. 357-362
    • Williams, D.R.1    Lees, A.J.2
  • 14
    • 33646187528 scopus 로고    scopus 로고
    • Primary progressive freezing gait: a syndrome with many causes
    • Factor S.A., Higgins D.S., Qian J. Primary progressive freezing gait: a syndrome with many causes. Neurology 2006, 66:411-414.
    • (2006) Neurology , vol.66 , pp. 411-414
    • Factor, S.A.1    Higgins, D.S.2    Qian, J.3
  • 15
    • 38049130310 scopus 로고    scopus 로고
    • Pure akinesia with gait freezing: a third clinical phenotype of progressive supranuclear palsy
    • Williams D.R., Holton J.L., Strand K., Revesz T., Lees A.J. Pure akinesia with gait freezing: a third clinical phenotype of progressive supranuclear palsy. Mov. Disord. 2007, 22:2235-2241.
    • (2007) Mov. Disord. , vol.22 , pp. 2235-2241
    • Williams, D.R.1    Holton, J.L.2    Strand, K.3    Revesz, T.4    Lees, A.J.5
  • 19
    • 26444516126 scopus 로고    scopus 로고
    • Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting
    • Scaravilli T., Tolosa E., Ferrer I. Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting. Mov. Disord. 2005, 20:21-28.
    • (2005) Mov. Disord. , vol.20 , pp. 21-28
    • Scaravilli, T.1    Tolosa, E.2    Ferrer, I.3
  • 21
    • 56749083283 scopus 로고    scopus 로고
    • Apraxia of speech and nonfluent aphasia: a new clinical marker for corticobasal degeneration and progressive supranuclear palsy
    • Josephs K.A., Duffy J.R. Apraxia of speech and nonfluent aphasia: a new clinical marker for corticobasal degeneration and progressive supranuclear palsy. Curr. Opin. Neurol. 2008, 21:688-692.
    • (2008) Curr. Opin. Neurol. , vol.21 , pp. 688-692
    • Josephs, K.A.1    Duffy, J.R.2
  • 22
    • 84871059690 scopus 로고    scopus 로고
    • Autopsy-proven progressive supranuclear palsy presenting as behavioral variant frontotemporal dementia
    • Hassan A., Parisi J.E., Josephs K.A. Autopsy-proven progressive supranuclear palsy presenting as behavioral variant frontotemporal dementia. Neurocase Neural Basis Cogn. 2013, 18:478-488.
    • (2013) Neurocase Neural Basis Cogn. , vol.18 , pp. 478-488
    • Hassan, A.1    Parisi, J.E.2    Josephs, K.A.3
  • 24
    • 84889087546 scopus 로고    scopus 로고
    • Early clinical features of patients with progressive supranuclear palsy with predominant cerebellar ataxia
    • Kanazawa M., Tada M., Onodera O., Takahashi H., Nishizawa M., Shimohata T. Early clinical features of patients with progressive supranuclear palsy with predominant cerebellar ataxia. Park. Relat. Disord. 2013, 19:1149-1151.
    • (2013) Park. Relat. Disord. , vol.19 , pp. 1149-1151
    • Kanazawa, M.1    Tada, M.2    Onodera, O.3    Takahashi, H.4    Nishizawa, M.5    Shimohata, T.6
  • 25
    • 84884973818 scopus 로고    scopus 로고
    • An autopsied case of progressive supranuclear palsy presenting with cerebellar ataxia and severe cerebellar involvement
    • Iwasaki Y., Mori K., Ito M., Tatsumi S., Mimuro M., Yoshida M. An autopsied case of progressive supranuclear palsy presenting with cerebellar ataxia and severe cerebellar involvement. Neuropathology 2013, 33:561-567.
    • (2013) Neuropathology , vol.33 , pp. 561-567
    • Iwasaki, Y.1    Mori, K.2    Ito, M.3    Tatsumi, S.4    Mimuro, M.5    Yoshida, M.6
  • 27
    • 79955728557 scopus 로고    scopus 로고
    • FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases
    • Rusina R., Kovacs G.G., Fiala J., Hort J., Ridzoň P., Holmerová I., Ströbel T., Matěj R. FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases. BMC Neurol. 2011, 11:50.
    • (2011) BMC Neurol. , vol.11 , pp. 50
    • Rusina, R.1    Kovacs, G.G.2    Fiala, J.3    Hort, J.4    Ridzoň, P.5    Holmerová, I.6    Ströbel, T.7    Matěj, R.8
  • 28
    • 26444560660 scopus 로고    scopus 로고
    • Parkinsonism-dementia complex of Guam
    • Steele J.C. Parkinsonism-dementia complex of Guam. Mov. Disord. 2005, 20:99-107.
    • (2005) Mov. Disord. , vol.20 , pp. 99-107
    • Steele, J.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.