Holton JL - Search Results

1

Prognosis and Neuropathologic Correlation of Clinical Subtypes of Parkinson Disease.

De Pablo-Fernández E, Lees AJ, Holton JL, Warner TT. De Pablo-Fernández E, et al. Among authors: holton jl. JAMA Neurol. 2019 Apr 1;76(4):470-479. doi: 10.1001/jamaneurol.2018.4377. JAMA Neurol. 2019. PMID: 30640364 Free PMC article.

2

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.

de Silva R, Lashley T, Gibb G, Hanger D, Hope A, Reid A, Bandopadhyay R, Utton M, Strand C, Jowett T, Khan N, Anderton B, Wood N, Holton J, Revesz T, Lees A. de Silva R, et al. Neuropathol Appl Neurobiol. 2003 Jun;29(3):288-302. doi: 10.1046/j.1365-2990.2003.00463.x. Neuropathol Appl Neurobiol. 2003. PMID: 12787326

3

Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP.

Morris HR, Osaki Y, Holton J, Lees AJ, Wood NW, Revesz T, Quinn N. Morris HR, et al. Neurology. 2003 Jul 8;61(1):102-4. doi: 10.1212/01.wnl.0000072325.27824.a5. Neurology. 2003. PMID: 12847166

4

Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes: broadening the clinical picture to include progressive supranuclear palsy.

Paviour DC, Lees AJ, Josephs KA, Ozawa T, Ganguly M, Strand C, Godbolt A, Howard RS, Revesz T, Holton JL. Paviour DC, et al. Among authors: holton jl. Brain. 2004 Nov;127(Pt 11):2441-51. doi: 10.1093/brain/awh265. Epub 2004 Sep 30. Brain. 2004. PMID: 15459024

5

The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations.

Ozawa T, Paviour D, Quinn NP, Josephs KA, Sangha H, Kilford L, Healy DG, Wood NW, Lees AJ, Holton JL, Revesz T. Ozawa T, et al. Among authors: holton jl. Brain. 2004 Dec;127(Pt 12):2657-71. doi: 10.1093/brain/awh303. Epub 2004 Oct 27. Brain. 2004. PMID: 15509623

6

Pathological substrate for regional distribution of increased atrophy rates in progressive supranuclear palsy.

Paviour DC, Schott JM, Stevens JM, Revesz T, Holton JL, Rossor MN, Lees AJ, Fox NC. Paviour DC, et al. Among authors: holton jl. J Neurol Neurosurg Psychiatry. 2004 Dec;75(12):1772-5. doi: 10.1136/jnnp.2003.033472. J Neurol Neurosurg Psychiatry. 2004. PMID: 15548504 Free PMC article.

7

A common LRRK2 mutation in idiopathic Parkinson's disease.

Gilks WP, Abou-Sleiman PM, Gandhi S, Jain S, Singleton A, Lees AJ, Shaw K, Bhatia KP, Bonifati V, Quinn NP, Lynch J, Healy DG, Holton JL, Revesz T, Wood NW. Gilks WP, et al. Among authors: holton jl. Lancet. 2005 Jan 29-Feb 4;365(9457):415-6. doi: 10.1016/S0140-6736(05)17830-1. Lancet. 2005. PMID: 15680457

8

Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism.

Williams DR, de Silva R, Paviour DC, Pittman A, Watt HC, Kilford L, Holton JL, Revesz T, Lees AJ. Williams DR, et al. Among authors: holton jl. Brain. 2005 Jun;128(Pt 6):1247-58. doi: 10.1093/brain/awh488. Epub 2005 Mar 23. Brain. 2005. PMID: 15788542

9

Neuronal intranuclear inclusion disease: report on a case originally diagnosed as dopa-responsive dystonia with Lewy bodies.

Paviour DC, Revesz T, Holton JL, Evans A, Olsson JE, Lees AJ. Paviour DC, et al. Among authors: holton jl. Mov Disord. 2005 Oct;20(10):1345-9. doi: 10.1002/mds.20559. Mov Disord. 2005. PMID: 15966005

10

UCHL-1 gene in multiple system atrophy: a haplotype tagging approach.

Healy DG, Abou-Sleiman PM, Quinn N, Ahmadi KR, Ozawa T, Kamm C, Wullner U, Oertel WH, Burk K, Dupont E, Pellecchia MT, Tolosa E, Gasser T, Holton JL, Revesz T, Goldstein DB, Lees AJ, Wood NW; European MSA Study Group. Healy DG, et al. Among authors: holton jl. Mov Disord. 2005 Oct;20(10):1338-43. doi: 10.1002/mds.20575. Mov Disord. 2005. PMID: 16007636

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