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Items: 1 to 20 of 679

1.

Increased tau burden in the cortices of progressive supranuclear palsy presenting with corticobasal syndrome.

Tsuboi Y, Josephs KA, Boeve BF, Litvan I, Caselli RJ, Caviness JN, Uitti RJ, Bott AD, Dickson DW.

Mov Disord. 2005 Aug;20(8):982-8.

PMID:
15834857
2.

Tau pathology in the olfactory bulb correlates with Braak stage, Lewy body pathology and apolipoprotein epsilon4.

Tsuboi Y, Wszolek ZK, Graff-Radford NR, Cookson N, Dickson DW.

Neuropathol Appl Neurobiol. 2003 Oct;29(5):503-10.

PMID:
14507342
3.

Atypical progressive supranuclear palsy underlying progressive apraxia of speech and nonfluent aphasia.

Josephs KA, Boeve BF, Duffy JR, Smith GE, Knopman DS, Parisi JE, Petersen RC, Dickson DW.

Neurocase. 2005 Aug;11(4):283-96.

PMID:
16093229
4.

4-repeat tauopathy sharing pathological and biochemical features of corticobasal degeneration and progressive supranuclear palsy.

Katsuse O, Iseki E, Arai T, Akiyama H, Togo T, Uchikado H, Kato M, de Silva R, Lees A, Kosaka K.

Acta Neuropathol. 2003 Sep;106(3):251-60. Epub 2003 Jun 11.

PMID:
12802605
5.

[The diagnostic challenge of corticobasal degeneration: distinction between clinical syndrome and pathology].

Kellner O, Sabova K, Neumann M, Jung HH.

Fortschr Neurol Psychiatr. 2011 Nov;79(11):660-7. doi: 10.1055/s-0031-1281740. Epub 2011 Oct 18. German.

PMID:
22009274
6.

Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease.

Rizzo G, Martinelli P, Manners D, Scaglione C, Tonon C, Cortelli P, Malucelli E, Capellari S, Testa C, Parchi P, Montagna P, Barbiroli B, Lodi R.

Brain. 2008 Oct;131(Pt 10):2690-700. doi: 10.1093/brain/awn195. Epub 2008 Sep 26.

PMID:
18819991
7.

Primary progressive aphasia as the initial manifestation of corticobasal degeneration and unusual tauopathies.

Ferrer I, Hernández I, Boada M, Llorente A, Rey MJ, Cardozo A, Ezquerra M, Puig B.

Acta Neuropathol. 2003 Nov;106(5):419-35. Epub 2003 Aug 29.

PMID:
12955398
8.

[A 65-year-old man with rigid-bradykinetic parkinsonism, vertical gaze palsy, difficulty of eye-lid opening, and marked pseudo-bulbar palsy].

Noda K, Kobayashi T, Matsuoka S, Takanashi M, Kanazawa A, Mizuno Y.

No To Shinkei. 2005 Jan;57(1):73-86. Japanese.

PMID:
15782604
9.

Does corticobasal degeneration exist? A clinicopathological re-evaluation.

Ling H, O'Sullivan SS, Holton JL, Revesz T, Massey LA, Williams DR, Paviour DC, Lees AJ.

Brain. 2010 Jul;133(Pt 7):2045-57. doi: 10.1093/brain/awq123.

PMID:
20584946
10.

Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains.

Ingelsson M, Ramasamy K, Russ C, Freeman SH, Orne J, Raju S, Matsui T, Growdon JH, Frosch MP, Ghetti B, Brown RH, Irizarry MC, Hyman BT.

Acta Neuropathol. 2007 Nov;114(5):471-9. Epub 2007 Aug 25.

PMID:
17721707
11.

Characteristics of progressive supranuclear palsy presenting with corticobasal syndrome: a cortical variant.

Ling H, de Silva R, Massey LA, Courtney R, Hondhamuni G, Bajaj N, Lowe J, Holton JL, Lees A, Revesz T.

Neuropathol Appl Neurobiol. 2014 Feb;40(2):149-63. doi: 10.1111/nan.12037. Erratum in: Neuropathol Appl Neurobiol. 2014 Jun;40(4):514. Ling, H [corrected to Ling, Helen].

12.

Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting.

Scaravilli T, Tolosa E, Ferrer I.

Mov Disord. 2005 Aug;20 Suppl 12:S21-8.

PMID:
16092076
14.

Different tau pathology pattern in two clinical phenotypes of progressive supranuclear palsy.

Jellinger KA.

Neurodegener Dis. 2008;5(6):339-46. doi: 10.1159/000121388. Epub 2008 Mar 18.

PMID:
18349518
15.

Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP.

Josephs KA, Petersen RC, Knopman DS, Boeve BF, Whitwell JL, Duffy JR, Parisi JE, Dickson DW.

Neurology. 2006 Jan 10;66(1):41-8.

PMID:
16401843
16.

Regional quantitative analysis of tau-positive neurons in progressive supranuclear palsy: comparison with Alzheimer's disease.

Li F, Iseki E, Odawara T, Kosaka K, Yagishita S, Amano N.

J Neurol Sci. 1998 Jul 15;159(1):73-81.

PMID:
9700707
17.

Lewy bodies in progressive supranuclear palsy represent an independent disease process.

Uchikado H, DelleDonne A, Ahmed Z, Dickson DW.

J Neuropathol Exp Neurol. 2006 Apr;65(4):387-95.

PMID:
16691119
18.

A clinicopathological study of vascular progressive supranuclear palsy: a multi-infarct disorder presenting as progressive supranuclear palsy.

Josephs KA, Ishizawa T, Tsuboi Y, Cookson N, Dickson DW.

Arch Neurol. 2002 Oct;59(10):1597-601.

PMID:
12374498
19.

Ballooned neurons in progressive supranuclear palsy are usually due to concurrent argyrophilic grain disease.

Togo T, Dickson DW.

Acta Neuropathol. 2002 Jul;104(1):53-6. Epub 2002 Apr 9.

PMID:
12070664
20.

[An 81-year-old woman with progressive motor disturbance, extrapyramidal features, dementia, and oculomotor palsy].

Urabe T, Mori H, Sumino S, Miwa H, Wakiya M, Shirai T, Takubo H, Mizuno Y.

No To Shinkei. 1998 Mar;50(3):291-301. Japanese.

PMID:
9566008

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