Holton JL - Search Results

1

The phenomenon of disproportionate antecollis in Parkinson's disease and multiple system atrophy.

van de Warrenburg BP, Cordivari C, Ryan AM, Phadke R, Holton JL, Bhatia KP, Hanna MG, Quinn NP. van de Warrenburg BP, et al. Among authors: holton jl. Mov Disord. 2007 Dec;22(16):2325-31. doi: 10.1002/mds.21634. Mov Disord. 2007. PMID: 17960814

2

Human T cell leukaemia virus type I associated neuromuscular disease causing respiratory failure.

Littleton ET, Man WD, Holton JL, Landon DN, Hanna MG, Polkey MI, Taylor GP. Littleton ET, et al. Among authors: holton jl. J Neurol Neurosurg Psychiatry. 2002 May;72(5):650-2. doi: 10.1136/jnnp.72.5.650. J Neurol Neurosurg Psychiatry. 2002. PMID: 11971056 Free PMC article.

3

Tubular aggregate myopathy with abnormal pupils and skeletal deformities.

Jacques TS, Holton J, Watts PM, Wills AJ, Smith SE, Hanna MG. Jacques TS, et al. J Neurol Neurosurg Psychiatry. 2002 Sep;73(3):324-6. doi: 10.1136/jnnp.73.3.324. J Neurol Neurosurg Psychiatry. 2002. PMID: 12185172 Free PMC article.

4

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

5

Neurofilament inclusion body disease: a new proteinopathy?

Josephs KA, Holton JL, Rossor MN, Braendgaard H, Ozawa T, Fox NC, Petersen RC, Pearl GS, Ganguly M, Rosa P, Laursen H, Parisi JE, Waldemar G, Quinn NP, Dickson DW, Revesz T. Josephs KA, et al. Among authors: holton jl. Brain. 2003 Oct;126(Pt 10):2291-303. doi: 10.1093/brain/awg231. Epub 2003 Jul 22. Brain. 2003. PMID: 12876145

6

Unusual muscle disease in HIV infected patients.

Roedling S, Pearl D, Manji H, Hanna MG, Holton JL, Miller RF. Roedling S, et al. Among authors: holton jl. Sex Transm Infect. 2004 Aug;80(4):315-7. doi: 10.1136/sti.2003.008474. Sex Transm Infect. 2004. PMID: 15295133 Free PMC article. Review.

7

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

8

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

9

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

10

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.

Khan NL, Jain S, Lynch JM, Pavese N, Abou-Sleiman P, Holton JL, Healy DG, Gilks WP, Sweeney MG, Ganguly M, Gibbons V, Gandhi S, Vaughan J, Eunson LH, Katzenschlager R, Gayton J, Lennox G, Revesz T, Nicholl D, Bhatia KP, Quinn N, Brooks D, Lees AJ, Davis MB, Piccini P, Singleton AB, Wood NW. Khan NL, et al. Among authors: holton jl. Brain. 2005 Dec;128(Pt 12):2786-96. doi: 10.1093/brain/awh667. Epub 2005 Nov 4. Brain. 2005. PMID: 16272164

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