Quinn N - Search Results

1

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: quinn n. Brain. 2005 Dec;128(Pt 12):2786-96. doi: 10.1093/brain/awh667. Epub 2005 Nov 4. Brain. 2005. PMID: 16272164

2

The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of parkinsonism.

Healy DG, Abou-Sleiman PM, Ahmadi KR, Muqit MM, Bhatia KP, Quinn NP, Lees AJ, Latchmann DS, Goldstein DB, Wood NW. Healy DG, et al. Ann Neurol. 2004 Sep;56(3):329-35. doi: 10.1002/ana.20206. Ann Neurol. 2004. PMID: 15349859

3

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. Brain. 2004 Dec;127(Pt 12):2657-71. doi: 10.1093/brain/awh303. Epub 2004 Oct 27. Brain. 2004. PMID: 15509623

4

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. Lancet. 2005 Jan 29-Feb 4;365(9457):415-6. doi: 10.1016/S0140-6736(05)17830-1. Lancet. 2005. PMID: 15680457

5

Factors affecting the clinical outcome after neural transplantation in Parkinson's disease.

Piccini P, Pavese N, Hagell P, Reimer J, Björklund A, Oertel WH, Quinn NP, Brooks DJ, Lindvall O. Piccini P, et al. Among authors: quinn np. Brain. 2005 Dec;128(Pt 12):2977-86. doi: 10.1093/brain/awh649. Epub 2005 Oct 24. Brain. 2005. PMID: 16246865

6

UCHL-1 is not a Parkinson's disease susceptibility gene.

Healy DG, Abou-Sleiman PM, Casas JP, Ahmadi KR, Lynch T, Gandhi S, Muqit MM, Foltynie T, Barker R, Bhatia KP, Quinn NP, Lees AJ, Gibson JM, Holton JL, Revesz T, Goldstein DB, Wood NW. Healy DG, et al. Ann Neurol. 2006 Apr;59(4):627-33. doi: 10.1002/ana.20757. Ann Neurol. 2006. PMID: 16450370

7

In vivo assessment of brain monoamine systems in parkin gene carriers: a PET study.

Pavese N, Moore RY, Scherfler C, Khan NL, Hotton G, Quinn NP, Bhatia KP, Wood NW, Brooks DJ, Lees AJ, Piccini P. Pavese N, et al. Among authors: quinn np. Exp Neurol. 2010 Mar;222(1):120-4. doi: 10.1016/j.expneurol.2009.12.021. Epub 2010 Jan 4. Exp Neurol. 2010. PMID: 20043906

8

Striatal and cortical pre- and postsynaptic dopaminergic dysfunction in sporadic parkin-linked parkinsonism.

Scherfler C, Khan NL, Pavese N, Eunson L, Graham E, Lees AJ, Quinn NP, Wood NW, Brooks DJ, Piccini PP. Scherfler C, et al. Among authors: quinn np. Brain. 2004 Jun;127(Pt 6):1332-42. doi: 10.1093/brain/awh150. Epub 2004 Apr 16. Brain. 2004. PMID: 15090472

9

Parkin disease: a phenotypic study of a large case series.

Khan NL, Graham E, Critchley P, Schrag AE, Wood NW, Lees AJ, Bhatia KP, Quinn N. Khan NL, et al. Among authors: quinn n. Brain. 2003 Jun;126(Pt 6):1279-92. doi: 10.1093/brain/awg142. Brain. 2003. PMID: 12764051

10

The role of pathogenic DJ-1 mutations in Parkinson's disease.

Abou-Sleiman PM, Healy DG, Quinn N, Lees AJ, Wood NW. Abou-Sleiman PM, et al. Among authors: quinn n. Ann Neurol. 2003 Sep;54(3):283-6. doi: 10.1002/ana.10675. Ann Neurol. 2003. PMID: 12953260

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