Quinn NP - Search Results

1

Is sphincter electromyography a helpful investigation in the diagnosis of multiple system atrophy? A retrospective study with pathological diagnosis.

Paviour DC, Williams D, Fowler CJ, Quinn NP, Lees AJ. Paviour DC, et al. Among authors: quinn np. Mov Disord. 2005 Nov;20(11):1425-30. doi: 10.1002/mds.20584. Mov Disord. 2005. PMID: 16007638

2

A validation exercise on the new consensus criteria for multiple system atrophy.

Osaki Y, Ben-Shlomo Y, Lees AJ, Wenning GK, Quinn NP. Osaki Y, et al. Among authors: quinn np. Mov Disord. 2009 Nov 15;24(15):2272-6. doi: 10.1002/mds.22826. Mov Disord. 2009. PMID: 19845011

3

A comparison of depression, anxiety, and health status in patients with progressive supranuclear palsy and multiple system atrophy.

Schrag A, Sheikh S, Quinn NP, Lees AJ, Selai C, Mathias C, Litvan I, Lang AE, Bower JH, Burn DJ, Low P, Jahanshahi M. Schrag A, et al. Among authors: quinn np. Mov Disord. 2010 Jun 15;25(8):1077-81. doi: 10.1002/mds.22794. Mov Disord. 2010. PMID: 20535826

4

Accuracy of clinical diagnosis of progressive supranuclear palsy.

Osaki Y, Ben-Shlomo Y, Lees AJ, Daniel SE, Colosimo C, Wenning G, Quinn N. Osaki Y, et al. Mov Disord. 2004 Feb;19(2):181-9. doi: 10.1002/mds.10680. Mov Disord. 2004. PMID: 14978673

5

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. Mov Disord. 2005 Oct;20(10):1338-43. doi: 10.1002/mds.20575. Mov Disord. 2005. PMID: 16007636

6

Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registry.

Köllensperger M, Geser F, Ndayisaba JP, Boesch S, Seppi K, Ostergaard K, Dupont E, Cardozo A, Tolosa E, Abele M, Klockgether T, Yekhlef F, Tison F, Daniels C, Deuschl G, Coelho M, Sampaio C, Bozi M, Quinn N, Schrag A, Mathias CJ, Fowler C, Nilsson CF, Widner H, Schimke N, Oertel W, Del Sorbo F, Albanese A, Pellecchia MT, Barone P, Djaldetti R, Colosimo C, Meco G, Gonzalez-Mandly A, Berciano J, Gurevich T, Giladi N, Galitzky M, Rascol O, Kamm C, Gasser T, Siebert U, Poewe W, Wenning GK; EMSA-SG. Köllensperger M, et al. Mov Disord. 2010 Nov 15;25(15):2604-12. doi: 10.1002/mds.23192. Mov Disord. 2010. PMID: 20922810

7

Adult-onset tic disorder, motor stereotypies, and behavioural disturbance associated with antibasal ganglia antibodies.

Edwards MJ, Dale RC, Church AJ, Trikouli E, Quinn NP, Lees AJ, Giovannoni G, Bhatia KP. Edwards MJ, et al. Among authors: quinn np. Mov Disord. 2004 Oct;19(10):1190-6. doi: 10.1002/mds.20126. Mov Disord. 2004. PMID: 15390017

8

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

9

Upregulation of dopamine D2 receptors in dopaminergic drug-naive patients with Parkin gene mutations.

Scherfler C, Khan NL, Pavese N, Lees AJ, Quinn NP, Brooks DJ, Piccini PP. Scherfler C, et al. Among authors: quinn np. Mov Disord. 2006 Jun;21(6):783-8. doi: 10.1002/mds.20811. Mov Disord. 2006. PMID: 16511856

10

NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach.

Healy DG, Abou-Sleiman PM, Ahmadi KR, Gandhi S, Muqit MM, Bhatia KP, Quinn NP, Lees AJ, Holton JL, Revesz T, Wood NW. Healy DG, et al. Among authors: quinn np. Mov Disord. 2006 Nov;21(11):1960-3. doi: 10.1002/mds.21018. Mov Disord. 2006. PMID: 16977628

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