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Volumn 45, Issue 3, 2011, Pages 343-349

Parkinsonism and frontotemporal dementia: The clinical overlap

Author keywords

Corticobasal degeneration; Corticobasal syndrome; Frontotemporal dementia; Frontotemporal lobar degeneration; Parkinsonism; Progressive supranuclear palsy

Indexed keywords

N ACETYLASPARTIC ACID;

EID: 80855123673     PISSN: 08958696     EISSN: 15591166     Source Type: Journal    
DOI: 10.1007/s12031-011-9632-1     Document Type: Conference Paper
Times cited : (47)

References (54)
  • 1
    • 34347359543 scopus 로고    scopus 로고
    • Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation
    • 17318302 10.1007/s00702-007-0632-9 1:STN:280:DC%2BD2szns12nsQ%3D%3D
    • Y Baba MC Baker BI Le, et al. 2007 Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation J Neural Transm 114 7 947 950 17318302 10.1007/s00702-007-0632-9 1:STN:280:DC%2BD2szns12nsQ%3D%3D
    • (2007) J Neural Transm , vol.114 , Issue.7 , pp. 947-950
    • Baba, Y.1    Baker, M.C.2    Le, B.I.3
  • 2
    • 33746919083 scopus 로고    scopus 로고
    • Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
    • 16862116 10.1038/nature05016 1:CAS:528:DC%2BD28XosVOgurc%3D
    • M Baker IR Mackenzie SM Pickering-Brown, et al. 2006 Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 Nature 442 7105 916 919 16862116 10.1038/nature05016 1:CAS:528: DC%2BD28XosVOgurc%3D
    • (2006) Nature , vol.442 , Issue.7105 , pp. 916-919
    • Baker, M.1    MacKenzie, I.R.2    Pickering-Brown, S.M.3
  • 3
    • 0022560086 scopus 로고
    • Loss of striatal [76Br]bromospiperone binding sites demonstrated by positron tomography in progressive supranuclear palsy
    • 3485639 10.1038/jcbfm.1986.26 1:STN:280:DyaL287mvVGrsw%3D%3D
    • JC Baron B Maziere C Loc'h 1986 Loss of striatal [76Br]bromospiperone binding sites demonstrated by positron tomography in progressive supranuclear palsy J Cereb Blood Flow Metab 6 2 131 136 3485639 10.1038/jcbfm.1986.26 1:STN:280:DyaL287mvVGrsw%3D%3D
    • (1986) J Cereb Blood Flow Metab , vol.6 , Issue.2 , pp. 131-136
    • Baron, J.C.1    Maziere, B.2    Loc'H, C.3
  • 4
    • 42249085980 scopus 로고    scopus 로고
    • Refining frontotemporal dementia with parkinsonism linked to chromosome 17: Introducing FTDP-17 (MAPT) and FTDP-17 (PGRN)
    • 18413467 10.1001/archneur.65.4.460
    • BF Boeve M Hutton 2008 Refining frontotemporal dementia with parkinsonism linked to chromosome 17: introducing FTDP-17 (MAPT) and FTDP-17 (PGRN) Arch Neurol 65 4 460 464 18413467 10.1001/archneur.65.4.460
    • (2008) Arch Neurol , vol.65 , Issue.4 , pp. 460-464
    • Boeve, B.F.1    Hutton, M.2
  • 5
    • 33750576831 scopus 로고    scopus 로고
    • Frontotemporal dementia and parkinsonism associated with the IVS1 + 1G->A mutation in progranulin: A clinicopathologic study
    • 17030535 10.1093/brain/awl268
    • BF Boeve M Baker DW Dickson, et al. 2006 Frontotemporal dementia and parkinsonism associated with the IVS1 + 1G->A mutation in progranulin: a clinicopathologic study Brain 129 Pt 11 3103 3114 17030535 10.1093/brain/awl268
    • (2006) Brain , vol.129 , Issue.PART 11 , pp. 3103-3114
    • Boeve, B.F.1    Baker, M.2    Dickson, D.W.3
  • 6
    • 58149229648 scopus 로고    scopus 로고
    • Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy
    • 18971445 10.1212/01.wnl.0000335941.68602.39 1:CAS:528:DC%2BD1cXhtlylurjP
    • B Borroni M Malinverno F Gardoni, et al. 2008 Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy Neurology 71 22 1796 1803 18971445 10.1212/01.wnl.0000335941.68602.39 1:CAS:528:DC%2BD1cXhtlylurjP
    • (2008) Neurology , vol.71 , Issue.22 , pp. 1796-1803
    • Borroni, B.1    Malinverno, M.2    Gardoni, F.3
  • 7
    • 77955000583 scopus 로고    scopus 로고
    • VEGF haplotypes are associated with increased risk to progressive supranuclear palsy and corticobasal syndrome
    • 20413880 1:CAS:528:DC%2BC3cXptFGlt7s%3D
    • B Borroni BR Del S Goldwurm, et al. 2010 VEGF haplotypes are associated with increased risk to progressive supranuclear palsy and corticobasal syndrome J Alzheimers Dis 21 1 87 94 20413880 1:CAS:528:DC%2BC3cXptFGlt7s%3D
    • (2010) J Alzheimers Dis , vol.21 , Issue.1 , pp. 87-94
    • Borroni, B.1    Del, B.R.2    Goldwurm, S.3
  • 8
    • 0026612088 scopus 로고
    • Striatal D2 receptor status in patients with Parkinson's disease, striatonigral degeneration, and progressive supranuclear palsy, measured with 11C-raclopride and positron emission tomography
    • 1575457 10.1002/ana.410310209 1:STN:280:DyaK383ks1ClsQ%3D%3D
    • DJ Brooks V Ibanez GV Sawle, et al. 1992 Striatal D2 receptor status in patients with Parkinson's disease, striatonigral degeneration, and progressive supranuclear palsy, measured with 11C-raclopride and positron emission tomography Ann Neurol 31 2 184 192 1575457 10.1002/ana.410310209 1:STN:280:DyaK383ks1ClsQ%3D%3D
    • (1992) Ann Neurol , vol.31 , Issue.2 , pp. 184-192
    • Brooks, D.J.1    Ibanez, V.2    Sawle, G.V.3
  • 9
    • 34447096691 scopus 로고    scopus 로고
    • Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: Consensus of the Consortium for Frontotemporal Lobar Degeneration
    • 10.1007/s00401-007-0237-2
    • NJ Cairns EH Bigio IR Mackenzie, et al. 2007 Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration Acta Neuropathol (Berl) 114 1 5 22 10.1007/s00401-007-0237-2
    • (2007) Acta Neuropathol (Berl) , vol.114 , Issue.1 , pp. 5-22
    • Cairns, N.J.1    Bigio, E.H.2    MacKenzie, I.R.3
  • 10
    • 20444436869 scopus 로고    scopus 로고
    • FDG PET in the differential diagnosis of parkinsonian disorders
    • 15955501 10.1016/j.neuroimage.2005.03.012
    • T Eckert A Barnes V Dhawan, et al. 2005 FDG PET in the differential diagnosis of parkinsonian disorders Neuroimage 26 3 912 921 15955501 10.1016/j.neuroimage.2005.03.012
    • (2005) Neuroimage , vol.26 , Issue.3 , pp. 912-921
    • Eckert, T.1    Barnes, A.2    Dhawan, V.3
  • 11
    • 0029996072 scopus 로고    scopus 로고
    • Progressive supranuclear palsy presenting with dynamic aphasia
    • 8774405 10.1136/jnnp.60.4.403 1:STN:280:DyaK28zntVGjuw%3D%3D
    • T Esmonde E Giles J Xuereb, et al. 1996 Progressive supranuclear palsy presenting with dynamic aphasia J Neurol Neurosurg Psychiatr 60 4 403 410 8774405 10.1136/jnnp.60.4.403 1:STN:280:DyaK28zntVGjuw%3D%3D
    • (1996) J Neurol Neurosurg Psychiatr , vol.60 , Issue.4 , pp. 403-410
    • Esmonde, T.1    Giles, E.2    Xuereb, J.3
  • 12
    • 59149097039 scopus 로고    scopus 로고
    • DCTN1 mutations in Perry syndrome
    • 19136952 10.1038/ng.293 1:CAS:528:DC%2BD1MXktVamtw%3D%3D
    • MJ Farrer MM Hulihan JM Kachergus, et al. 2009 DCTN1 mutations in Perry syndrome Nat Genet 41 2 163 165 19136952 10.1038/ng.293 1:CAS:528: DC%2BD1MXktVamtw%3D%3D
    • (2009) Nat Genet , vol.41 , Issue.2 , pp. 163-165
    • Farrer, M.J.1    Hulihan, M.M.2    Kachergus, J.M.3
  • 13
    • 79751494911 scopus 로고    scopus 로고
    • Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN)
    • 20930269 1:CAS:528:DC%2BC3cXhs1aks77L
    • T Gabryelewicz M Masellis M Berdynski, et al. 2010 Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN) J Alzheimers Dis 22 4 1123 1133 20930269 1:CAS:528:DC%2BC3cXhs1aks77L
    • (2010) J Alzheimers Dis , vol.22 , Issue.4 , pp. 1123-1133
    • Gabryelewicz, T.1    Masellis, M.2    Berdynski, M.3
  • 14
    • 79951493266 scopus 로고    scopus 로고
    • An algorithm for genetic testing of frontotemporal lobar degeneration
    • 21282594 10.1212/WNL.0b013e31820a0d13 1:STN:280:DC%2BC3M7lsl2isQ%3D%3D
    • JS Goldman R Rademakers ED Huey, et al. 2011 An algorithm for genetic testing of frontotemporal lobar degeneration Neurology 76 5 475 483 21282594 10.1212/WNL.0b013e31820a0d13 1:STN:280:DC%2BC3M7lsl2isQ%3D%3D
    • (2011) Neurology , vol.76 , Issue.5 , pp. 475-483
    • Goldman, J.S.1    Rademakers, R.2    Huey, E.D.3
  • 15
    • 0042932772 scopus 로고    scopus 로고
    • Language function and dysfunction in corticobasal degeneration
    • 12939423
    • NL Graham T Bak K Patterson, et al. 2003 Language function and dysfunction in corticobasal degeneration Neurology 61 4 493 499 12939423
    • (2003) Neurology , vol.61 , Issue.4 , pp. 493-499
    • Graham, N.L.1    Bak, T.2    Patterson, K.3
  • 16
    • 33645815670 scopus 로고    scopus 로고
    • Penguins and hummingbirds: Midbrain atrophy in progressive supranuclear palsy
    • 16567726 10.1212/01.wnl.0000203342.77115.bf
    • K Groschel A Kastrup I Litvan, et al. 2006 Penguins and hummingbirds: midbrain atrophy in progressive supranuclear palsy Neurology 66 6 949 950 16567726 10.1212/01.wnl.0000203342.77115.bf
    • (2006) Neurology , vol.66 , Issue.6 , pp. 949-950
    • Groschel, K.1    Kastrup, A.2    Litvan, I.3
  • 17
    • 51449107701 scopus 로고    scopus 로고
    • Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases
    • 18464284 10.1002/mds.22078
    • RJ Guerreiro I Santana JM Bras, et al. 2008 Novel progranulin mutation: screening for PGRN mutations in a Portuguese series of FTD/CBS cases Mov Disord 23 9 1269 1273 18464284 10.1002/mds.22078
    • (2008) Mov Disord , vol.23 , Issue.9 , pp. 1269-1273
    • Guerreiro, R.J.1    Santana, I.2    Bras, J.M.3
  • 18
    • 0032543684 scopus 로고    scopus 로고
    • Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
    • 9641683 10.1038/31508 1:CAS:528:DyaK1cXktVyqsr0%3D
    • M Hutton CL Lendon P Rizzu, et al. 1998 Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 Nature 393 6686 702 705 9641683 10.1038/31508 1:CAS:528:DyaK1cXktVyqsr0%3D
    • (1998) Nature , vol.393 , Issue.6686 , pp. 702-705
    • Hutton, M.1    Lendon, C.L.2    Rizzu, P.3
  • 19
    • 0034877085 scopus 로고    scopus 로고
    • Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells
    • 11585254 1:CAS:528:DC%2BD3MXmtFKntr0%3D
    • E Iseki T Matsumura W Marui, et al. 2001 Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells Acta Neuropathol 102 3 285 292 11585254 1:CAS:528:DC%2BD3MXmtFKntr0%3D
    • (2001) Acta Neuropathol , vol.102 , Issue.3 , pp. 285-292
    • Iseki, E.1    Matsumura, T.2    Marui, W.3
  • 20
    • 56749083283 scopus 로고    scopus 로고
    • Apraxia of speech and nonfluent aphasia: A new clinical marker for corticobasal degeneration and progressive supranuclear palsy
    • 18989114 10.1097/WCO.0b013e3283168ddd
    • KA Josephs JR Duffy 2008 Apraxia of speech and nonfluent aphasia: a new clinical marker for corticobasal degeneration and progressive supranuclear palsy Curr Opin Neurol 21 6 688 692 18989114 10.1097/WCO.0b013e3283168ddd
    • (2008) Curr Opin Neurol , vol.21 , Issue.6 , pp. 688-692
    • Josephs, K.A.1    Duffy, J.R.2
  • 21
    • 23844508831 scopus 로고    scopus 로고
    • Survival in two variants of tau-negative frontotemporal lobar degeneration: FTLD-U vs FTLD-MND
    • 16116138 10.1212/01.wnl.0000173178.67986.7f 1:STN:280: DC%2BD2MvkvFCmsw%3D%3D
    • KA Josephs DS Knopman JL Whitwell, et al. 2005 Survival in two variants of tau-negative frontotemporal lobar degeneration: FTLD-U vs FTLD-MND Neurology 65 4 645 647 16116138 10.1212/01.wnl.0000173178.67986.7f 1:STN:280: DC%2BD2MvkvFCmsw%3D%3D
    • (2005) Neurology , vol.65 , Issue.4 , pp. 645-647
    • Josephs, K.A.1    Knopman, D.S.2    Whitwell, J.L.3
  • 22
    • 33745095038 scopus 로고    scopus 로고
    • Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech
    • 16613895 10.1093/brain/awl078
    • KA Josephs JR Duffy EA Strand, et al. 2006 Clinicopathological and imaging correlates of progressive aphasia and apraxia of speech Brain 129 Pt 6 1385 1398 16613895 10.1093/brain/awl078
    • (2006) Brain , vol.129 , Issue.PART 6 , pp. 1385-1398
    • Josephs, K.A.1    Duffy, J.R.2    Strand, E.A.3
  • 23
    • 33645729013 scopus 로고    scopus 로고
    • Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP
    • 16401843 10.1212/01.wnl.0000191307.69661.c3 1:STN:280: DC%2BD28%2Fhs1Kgtg%3D%3D
    • KA Josephs RC Petersen DS Knopman, et al. 2006 Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP Neurology 66 1 41 48 16401843 10.1212/01.wnl.0000191307.69661.c3 1:STN:280:DC%2BD28%2Fhs1Kgtg%3D%3D
    • (2006) Neurology , vol.66 , Issue.1 , pp. 41-48
    • Josephs, K.A.1    Petersen, R.C.2    Knopman, D.S.3
  • 24
    • 77953848935 scopus 로고    scopus 로고
    • Caudate atrophy on MRI is a characteristic feature of FTLD-FUS
    • 20236174 10.1111/j.1468-1331.2010.02975.x 1:STN:280: DC%2BC3cnotFCqsQ%3D%3D
    • KA Josephs JL Whitwell JE Parisi, et al. 2010 Caudate atrophy on MRI is a characteristic feature of FTLD-FUS Eur J Neurol 17 7 969 975 20236174 10.1111/j.1468-1331.2010.02975.x 1:STN:280:DC%2BC3cnotFCqsQ%3D%3D
    • (2010) Eur J Neurol , vol.17 , Issue.7 , pp. 969-975
    • Josephs, K.A.1    Whitwell, J.L.2    Parisi, J.E.3
  • 25
    • 62349102691 scopus 로고    scopus 로고
    • Prominent phenotypic variability associated with mutations in progranulin
    • 17949857 10.1016/j.neurobiolaging.2007.08.022 1:CAS:528: DC%2BD1MXjsVKqt7g%3D
    • BJ Kelley W Haidar BF Boeve, et al. 2009 Prominent phenotypic variability associated with mutations in progranulin Neurobiol Aging 30 5 739 751 17949857 10.1016/j.neurobiolaging.2007.08.022 1:CAS:528:DC%2BD1MXjsVKqt7g%3D
    • (2009) Neurobiol Aging , vol.30 , Issue.5 , pp. 739-751
    • Kelley, B.J.1    Haidar, W.2    Boeve, B.F.3
  • 26
    • 36849072562 scopus 로고    scopus 로고
    • Patterns of MRI atrophy in tau positive and ubiquitin positive frontotemporal lobar degeneration
    • 17615169 10.1136/jnnp.2006.114231 1:STN:280:DC%2BD2snot1Cmtg%3D%3D
    • EJ Kim GD Rabinovici WW Seeley, et al. 2007 Patterns of MRI atrophy in tau positive and ubiquitin positive frontotemporal lobar degeneration J Neurol Neurosurg Psychiatr 78 12 1375 1378 17615169 10.1136/jnnp.2006.114231 1:STN:280:DC%2BD2snot1Cmtg%3D%3D
    • (2007) J Neurol Neurosurg Psychiatr , vol.78 , Issue.12 , pp. 1375-1378
    • Kim, E.J.1    Rabinovici, G.D.2    Seeley, W.W.3
  • 27
    • 80855162337 scopus 로고    scopus 로고
    • Neuropathologic features of corticobasal degeneration presenting as corticobasal syndrome or Richardson syndrome
    • (in press)
    • Kouri N, Murray ME, Hassan A, et al. (2011) Neuropathologic features of corticobasal degeneration presenting as corticobasal syndrome or Richardson syndrome. Brain (in press).
    • (2011) Brain
    • Kouri, N.1    Murray, M.E.2    Hassan, A.3
  • 28
    • 54449096081 scopus 로고    scopus 로고
    • White matter tauopathy with globular glial inclusions: A distinct sporadic frontotemporal lobar degeneration
    • 18800011 10.1097/NEN.0b013e318187a80f
    • GG Kovacs K Majtenyi S Spina, et al. 2008 White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration J Neuropathol Exp Neurol 67 10 963 975 18800011 10.1097/NEN.0b013e318187a80f
    • (2008) J Neuropathol Exp Neurol , vol.67 , Issue.10 , pp. 963-975
    • Kovacs, G.G.1    Majtenyi, K.2    Spina, S.3
  • 29
    • 0027967910 scopus 로고
    • "Apraxia of lid opening," a focal eyelid dystonia: Clinical study of 32 patients
    • 7845400 10.1002/mds.870090605 1:STN:280:DyaK2M7kslyqtA%3D%3D
    • P Krack MH Marion 1994 "Apraxia of lid opening," a focal eyelid dystonia: clinical study of 32 patients Mov Disord 9 6 610 615 7845400 10.1002/mds.870090605 1:STN:280:DyaK2M7kslyqtA%3D%3D
    • (1994) Mov Disord , vol.9 , Issue.6 , pp. 610-615
    • Krack, P.1    Marion, M.H.2
  • 30
    • 80051535251 scopus 로고    scopus 로고
    • Clinicopathological correlations in corticobasal degeneration
    • 21823158 10.1002/ana.22424
    • SE Lee GD Rabinovici MC Mayo, et al. 2011 Clinicopathological correlations in corticobasal degeneration Ann Neurol 70 2 327 340 21823158 10.1002/ana.22424
    • (2011) Ann Neurol , vol.70 , Issue.2 , pp. 327-340
    • Lee, S.E.1    Rabinovici, G.D.2    Mayo, M.C.3
  • 31
    • 77954362718 scopus 로고    scopus 로고
    • Does corticobasal degeneration exist? A clinicopathological re-evaluation
    • 20584946 10.1093/brain/awq123
    • H Ling SS O'Sullivan JL Holton, et al. 2010 Does corticobasal degeneration exist? A clinicopathological re-evaluation Brain 133 Pt 7 2045 2057 20584946 10.1093/brain/awq123
    • (2010) Brain , vol.133 , Issue.PART 7 , pp. 2045-2057
    • Ling, H.1    O'Sullivan, S.S.2    Holton, J.L.3
  • 32
    • 57049105123 scopus 로고    scopus 로고
    • Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: Consensus recommendations
    • 19015862 10.1007/s00401-008-0460-5
    • IR Mackenzie M Neumann EH Bigio, et al. 2009 Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations Acta Neuropathol 117 1 15 18 19015862 10.1007/s00401-008-0460-5
    • (2009) Acta Neuropathol , vol.117 , Issue.1 , pp. 15-18
    • MacKenzie, I.R.1    Neumann, M.2    Bigio, E.H.3
  • 33
    • 0038353463 scopus 로고    scopus 로고
    • Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP
    • 12847166 1:CAS:528:DC%2BD3sXks1OktLs%3D
    • HR Morris Y Osaki J Holton, et al. 2003 Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP Neurology 61 1 102 104 12847166 1:CAS:528:DC%2BD3sXks1OktLs%3D
    • (2003) Neurology , vol.61 , Issue.1 , pp. 102-104
    • Morris, H.R.1    Osaki, Y.2    Holton, J.3
  • 34
    • 77951841861 scopus 로고    scopus 로고
    • Perry syndrome due to the DCTN1 G71R mutation: A distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure
    • 20437543 10.1002/mds.22950
    • V Newsway M Fish JD Rohrer, et al. 2010 Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure Mov Disord 25 6 767 770 20437543 10.1002/mds.22950
    • (2010) Mov Disord , vol.25 , Issue.6 , pp. 767-770
    • Newsway, V.1    Fish, M.2    Rohrer, J.D.3
  • 35
    • 12744255024 scopus 로고    scopus 로고
    • Orofacial apraxia in corticobasal degeneration, progressive supranuclear palsy, multiple system atrophy and Parkinson's disease
    • 15592726 10.1007/s00415-004-0530-0
    • C Ozsancak P Auzou K Dujardin, et al. 2004 Orofacial apraxia in corticobasal degeneration, progressive supranuclear palsy, multiple system atrophy and Parkinson's disease J Neurol 251 11 1317 1323 15592726 10.1007/s00415-004-0530-0
    • (2004) J Neurol , vol.251 , Issue.11 , pp. 1317-1323
    • Ozsancak, C.1    Auzou, P.2    Dujardin, K.3
  • 36
    • 0035134195 scopus 로고    scopus 로고
    • Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene
    • 11220749 10.1002/1531-8249(20010201)49:2<263::AID-ANA50>3.0.CO;2-K 1:CAS:528:DC%2BD3MXhsVymurc%3D
    • P Pastor E Pastor C Carnero, et al. 2001 Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene Ann Neurol 49 2 263 267 11220749 10.1002/1531-8249(20010201)49: 2<263::AID-ANA50>3.0.CO;2-K 1:CAS:528:DC%2BD3MXhsVymurc%3D
    • (2001) Ann Neurol , vol.49 , Issue.2 , pp. 263-267
    • Pastor, P.1    Pastor, E.2    Carnero, C.3
  • 37
    • 17544391170 scopus 로고    scopus 로고
    • Longitudinal ocular motor study in corticobasal degeneration and progressive supranuclear palsy
    • 10720270 1:STN:280:DC%2BD3c7otlaisA%3D%3D
    • S Rivaud-Pechoux M Vidailhet G Gallouedec, et al. 2000 Longitudinal ocular motor study in corticobasal degeneration and progressive supranuclear palsy Neurology 54 5 1029 1032 10720270 1:STN:280:DC%2BD3c7otlaisA%3D%3D
    • (2000) Neurology , vol.54 , Issue.5 , pp. 1029-1032
    • Rivaud-Pechoux, S.1    Vidailhet, M.2    Gallouedec, G.3
  • 38
    • 70449365115 scopus 로고    scopus 로고
    • The heritability and genetics of frontotemporal lobar degeneration
    • 19884572 10.1212/WNL.0b013e3181bf997a 1:CAS:528:DC%2BD1MXhtlCmsrjP
    • JD Rohrer R Guerreiro J Vandrovcova, et al. 2009 The heritability and genetics of frontotemporal lobar degeneration Neurology 73 18 1451 1456 19884572 10.1212/WNL.0b013e3181bf997a 1:CAS:528:DC%2BD1MXhtlCmsrjP
    • (2009) Neurology , vol.73 , Issue.18 , pp. 1451-1456
    • Rohrer, J.D.1    Guerreiro, R.2    Vandrovcova, J.3
  • 39
    • 77956227571 scopus 로고    scopus 로고
    • Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations
    • 20045477 10.1016/j.neuroimage.2009.12.088 1:CAS:528:DC%2BC3cXhtFWqtrrN
    • JD Rohrer GR Ridgway M Modat, et al. 2010 Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations Neuroimage 53 3 1070 1076 20045477 10.1016/j.neuroimage.2009.12.088 1:CAS:528:DC%2BC3cXhtFWqtrrN
    • (2010) Neuroimage , vol.53 , Issue.3 , pp. 1070-1076
    • Rohrer, J.D.1    Ridgway, G.R.2    Modat, M.3
  • 40
    • 79953301545 scopus 로고    scopus 로고
    • Novel L284R MAPT mutation in a family with an autosomal dominant progressive supranuclear palsy syndrome
    • 20838030 10.1159/000319454 1:CAS:528:DC%2BC3MXjvFKqtLY%3D
    • JD Rohrer D Paviour J Vandrovcova, et al. 2011 Novel L284R MAPT mutation in a family with an autosomal dominant progressive supranuclear palsy syndrome Neurodegener Dis 8 3 149 152 20838030 10.1159/000319454 1:CAS:528: DC%2BC3MXjvFKqtLY%3D
    • (2011) Neurodegener Dis , vol.8 , Issue.3 , pp. 149-152
    • Rohrer, J.D.1    Paviour, D.2    Vandrovcova, J.3
  • 41
    • 52949094629 scopus 로고    scopus 로고
    • Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis
    • 18802454 10.1371/journal.pgen.1000193
    • NJ Rutherford YJ Zhang M Baker, et al. 2008 Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis PLoS Genet 4 9 e1000193 18802454 10.1371/journal.pgen.1000193
    • (2008) PLoS Genet , vol.4 , Issue.9 , pp. 1000193
    • Rutherford, N.J.1    Zhang, Y.J.2    Baker, M.3
  • 42
    • 78649796826 scopus 로고    scopus 로고
    • Low serum progranulin predicts the presence of mutations: A prospective study
    • 20858962 1:CAS:528:DC%2BC3cXhsFSqt7zF
    • EC Schofield GM Halliday J Kwok, et al. 2010 Low serum progranulin predicts the presence of mutations: a prospective study J Alzheimers Dis 22 3 981 984 20858962 1:CAS:528:DC%2BC3cXhsFSqt7zF
    • (2010) J Alzheimers Dis , vol.22 , Issue.3 , pp. 981-984
    • Schofield, E.C.1    Halliday, G.M.2    Kwok, J.3
  • 43
    • 69949189621 scopus 로고    scopus 로고
    • Is the pathology of corticobasal syndrome predictable in life?
    • 19533751 10.1002/mds.22558
    • BP Shelley JR Hodges CM Kipps, et al. 2009 Is the pathology of corticobasal syndrome predictable in life? Mov Disord 24 11 1593 1599 19533751 10.1002/mds.22558
    • (2009) Mov Disord , vol.24 , Issue.11 , pp. 1593-1599
    • Shelley, B.P.1    Hodges, J.R.2    Kipps, C.M.3
  • 44
    • 38349113827 scopus 로고    scopus 로고
    • The tau S305S mutation causes frontotemporal dementia with parkinsonism
    • 18093153 10.1111/j.1468-1331.2007.02017.x 1:STN:280: DC%2BD1c%2FmtFGrsg%3D%3D
    • L Skoglund M Viitanen H Kalimo, et al. 2008 The tau S305S mutation causes frontotemporal dementia with parkinsonism Eur J Neurol 15 2 156 161 18093153 10.1111/j.1468-1331.2007.02017.x 1:STN:280:DC%2BD1c%2FmtFGrsg%3D%3D
    • (2008) Eur J Neurol , vol.15 , Issue.2 , pp. 156-161
    • Skoglund, L.1    Viitanen, M.2    Kalimo, H.3
  • 45
    • 0141958877 scopus 로고    scopus 로고
    • A case of dementia parkinsonism resembling progressive supranuclear palsy due to mutation in the tau protein gene
    • 14568818 10.1001/archneur.60.10.1454
    • P Soliveri G Rossi D Monza, et al. 2003 A case of dementia parkinsonism resembling progressive supranuclear palsy due to mutation in the tau protein gene Arch Neurol 60 10 1454 1456 14568818 10.1001/archneur.60.10.1454
    • (2003) Arch Neurol , vol.60 , Issue.10 , pp. 1454-1456
    • Soliveri, P.1    Rossi, G.2    Monza, D.3
  • 46
    • 34948898536 scopus 로고    scopus 로고
    • Corticobasal syndrome associated with the A9D progranulin mutation
    • 17917583 10.1097/nen.0b013e3181567873 1:CAS:528:DC%2BD2sXht1yiur%2FF
    • S Spina JR Murrell ED Huey, et al. 2007 Corticobasal syndrome associated with the A9D progranulin mutation J Neuropathol Exp Neurol 66 10 892 900 17917583 10.1097/nen.0b013e3181567873 1:CAS:528:DC%2BD2sXht1yiur%2FF
    • (2007) J Neuropathol Exp Neurol , vol.66 , Issue.10 , pp. 892-900
    • Spina, S.1    Murrell, J.R.2    Huey, E.D.3
  • 47
    • 0030801539 scopus 로고    scopus 로고
    • Proton magnetic resonance spectroscopic imaging in progressive supranuclear palsy, Parkinson's disease and corticobasal degeneration
    • 9313638 10.1093/brain/120.9.1541
    • G Tedeschi I Litvan S Bonavita, et al. 1997 Proton magnetic resonance spectroscopic imaging in progressive supranuclear palsy, Parkinson's disease and corticobasal degeneration Brain 120 Pt 9 1541 1552 9313638 10.1093/brain/120.9. 1541
    • (1997) Brain , vol.120 , Issue.PART 9 , pp. 1541-1552
    • Tedeschi, G.1    Litvan, I.2    Bonavita, S.3
  • 48
    • 0037058799 scopus 로고    scopus 로고
    • Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)
    • 12473774 1:STN:280:DC%2BD38jhtFyguw%3D%3D
    • Y Tsuboi M Baker ML Hutton, et al. 2002 Clinical and genetic studies of families with the tau N279K mutation (FTDP-17) Neurology 59 11 1791 1793 12473774 1:STN:280:DC%2BD38jhtFyguw%3D%3D
    • (2002) Neurology , vol.59 , Issue.11 , pp. 1791-1793
    • Tsuboi, Y.1    Baker, M.2    Hutton, M.L.3
  • 49
    • 0028176892 scopus 로고
    • Eye movements in parkinsonian syndromes
    • 8154868 10.1002/ana.410350408 1:STN:280:DyaK2c3gs1Sisw%3D%3D
    • M Vidailhet S Rivaud N Gouider-Khouja, et al. 1994 Eye movements in parkinsonian syndromes Ann Neurol 35 4 420 426 8154868 10.1002/ana.410350408 1:STN:280:DyaK2c3gs1Sisw%3D%3D
    • (1994) Ann Neurol , vol.35 , Issue.4 , pp. 420-426
    • Vidailhet, M.1    Rivaud, S.2    Gouider-Khouja, N.3
  • 50
    • 1842483843 scopus 로고    scopus 로고
    • Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
    • 15034582 10.1038/ng1332 1:CAS:528:DC%2BD2cXis1aht70%3D
    • GD Watts J Wymer MJ Kovach, et al. 2004 Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein Nat Genet 36 4 377 381 15034582 10.1038/ng1332 1:CAS:528:DC%2BD2cXis1aht70%3D
    • (2004) Nat Genet , vol.36 , Issue.4 , pp. 377-381
    • Watts, G.D.1    Wymer, J.2    Kovach, M.J.3
  • 51
    • 78650834063 scopus 로고    scopus 로고
    • Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration?
    • 21172844 10.1212/WNL.0b013e31820203c2 1:STN:280:DC%2BC3M%2Flslaiug%3D%3D
    • JL Whitwell CR Jack Jr JE Parisi, et al. 2010 Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration? Neurology 75 24 2212 2220 21172844 10.1212/WNL.0b013e31820203c2 1:STN:280: DC%2BC3M%2Flslaiug%3D%3D
    • (2010) Neurology , vol.75 , Issue.24 , pp. 2212-2220
    • Whitwell, J.L.1    Jack Jr., C.R.2    Parisi, J.E.3
  • 52
    • 51449084344 scopus 로고    scopus 로고
    • Progranulin gene mutation with an unusual clinical and neuropathologic presentation
    • 18442119 10.1002/mds.22065
    • C Wider RJ Uitti ZK Wszolek, et al. 2008 Progranulin gene mutation with an unusual clinical and neuropathologic presentation Mov Disord 23 8 1168 1173 18442119 10.1002/mds.22065
    • (2008) Mov Disord , vol.23 , Issue.8 , pp. 1168-1173
    • Wider, C.1    Uitti, R.J.2    Wszolek, Z.K.3
  • 53
    • 0034907406 scopus 로고    scopus 로고
    • Progressive supranuclear palsy as a disease phenotype caused by the S305S tau gene mutation
    • 11459757 10.1093/brain/124.8.1666 1:STN:280:DC%2BD3MvksVOlsQ%3D%3D
    • ZK Wszolek Y Tsuboi RJ Uitti, et al. 2001 Progressive supranuclear palsy as a disease phenotype caused by the S305S tau gene mutation Brain 124 Pt 8 1666 1670 11459757 10.1093/brain/124.8.1666 1:STN:280:DC%2BD3MvksVOlsQ%3D%3D
    • (2001) Brain , vol.124 , Issue.PART 8 , pp. 1666-1670
    • Wszolek, Z.K.1    Tsuboi, Y.2    Uitti, R.J.3
  • 54
    • 79953137272 scopus 로고    scopus 로고
    • Neuropsychiatric symptoms of progressive supranuclear palsy in a dementia clinic
    • 21447110 10.1111/j.1479-8301.2010.00352.x
    • Y Yatabe M Hashimoto K Kaneda, et al. 2011 Neuropsychiatric symptoms of progressive supranuclear palsy in a dementia clinic Psychogeriatrics 11 1 54 59 21447110 10.1111/j.1479-8301.2010.00352.x
    • (2011) Psychogeriatrics , vol.11 , Issue.1 , pp. 54-59
    • Yatabe, Y.1    Hashimoto, M.2    Kaneda, K.3


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