Ozelius LJ - Search Results

1

Heterogeneity of presentation and outcome in the Irish rapid-onset dystonia-parkinsonism kindred.

McKeon A, Ozelius LJ, Hardiman O, Greenway MJ, Pittock SJ. McKeon A, et al. Among authors: ozelius lj. Mov Disord. 2007 Jul 15;22(9):1325-7. doi: 10.1002/mds.21335. Mov Disord. 2007. PMID: 17516473

2

ATP1A3 mutation in the first asian case of rapid-onset dystonia-parkinsonism.

Lee JY, Gollamudi S, Ozelius LJ, Kim JY, Jeon BS. Lee JY, et al. Among authors: ozelius lj. Mov Disord. 2007 Sep 15;22(12):1808-9. doi: 10.1002/mds.21638. Mov Disord. 2007. PMID: 17595045

3

Cognitive impairment in rapid-onset dystonia-parkinsonism.

Cook JF, Hill DF, Snively BM, Boggs N, Suerken CK, Haq I, Stacy M, McCall WV, Ozelius LJ, Sweadner KJ, Brashear A. Cook JF, et al. Among authors: ozelius lj. Mov Disord. 2014 Mar;29(3):344-50. doi: 10.1002/mds.25790. Epub 2014 Jan 16. Mov Disord. 2014. PMID: 24436111 Free PMC article. Clinical Trial.

4

Revising rapid-onset dystonia-parkinsonism: Broadening indications for ATP1A3 testing.

Haq IU, Snively BM, Sweadner KJ, Suerken CK, Cook JF, Ozelius LJ, Miller C, McCall WV, Whitlow CT, Brashear A. Haq IU, et al. Among authors: ozelius lj. Mov Disord. 2019 Oct;34(10):1528-1536. doi: 10.1002/mds.27801. Epub 2019 Jul 30. Mov Disord. 2019. PMID: 31361359 Free PMC article.

5

The endophenotype and the phenotype: temporal discrimination and adult-onset dystonia.

Hutchinson M, Kimmich O, Molloy A, Whelan R, Molloy F, Lynch T, Healy DG, Walsh C, Edwards MJ, Ozelius L, Reilly RB, O'Riordan S. Hutchinson M, et al. Mov Disord. 2013 Nov;28(13):1766-74. doi: 10.1002/mds.25676. Epub 2013 Oct 9. Mov Disord. 2013. PMID: 24108447 Free article.

6

Rapid-onset dystonia-parkinsonism: a fourth family consistent with linkage to chromosome 19q13.

Zaremba J, Mierzewska H, Lysiak Z, Kramer P, Ozelius LJ, Brashear A. Zaremba J, et al. Among authors: ozelius lj. Mov Disord. 2004 Dec;19(12):1506-10. doi: 10.1002/mds.20258. Mov Disord. 2004. PMID: 15390049

7

Inherited myoclonus-dystonia and epilepsy: further evidence of an association?

O'Riordan S, Ozelius LJ, de Carvalho Aguiar P, Hutchinson M, King M, Lynch T. O'Riordan S, et al. Among authors: ozelius lj. Mov Disord. 2004 Dec;19(12):1456-9. doi: 10.1002/mds.20224. Mov Disord. 2004. PMID: 15389977

8

New triggers and non-motor findings in a family with rapid-onset dystonia-parkinsonism.

Barbano RL, Hill DF, Snively BM, Light LS, Boggs N, McCall WV, Stacy M, Ozelius L, Sweadner KJ, Brashear A. Barbano RL, et al. Parkinsonism Relat Disord. 2012 Jul;18(6):737-41. doi: 10.1016/j.parkreldis.2012.03.020. Epub 2012 Apr 24. Parkinsonism Relat Disord. 2012. PMID: 22534615 Free PMC article.

9

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.

Brashear A, Dobyns WB, de Carvalho Aguiar P, Borg M, Frijns CJ, Gollamudi S, Green A, Guimaraes J, Haake BC, Klein C, Linazasoro G, Münchau A, Raymond D, Riley D, Saunders-Pullman R, Tijssen MA, Webb D, Zaremba J, Bressman SB, Ozelius LJ. Brashear A, et al. Among authors: ozelius lj. Brain. 2007 Mar;130(Pt 3):828-35. doi: 10.1093/brain/awl340. Epub 2007 Feb 4. Brain. 2007. PMID: 17282997

10

Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutations.

Raymond D, Saunders-Pullman R, de Carvalho Aguiar P, Schule B, Kock N, Friedman J, Harris J, Ford B, Frucht S, Heiman GA, Jennings D, Doheny D, Brin MF, de Leon Brin D, Multhaupt-Buell T, Lang AE, Kurlan R, Klein C, Ozelius L, Bressman S. Raymond D, et al. Mov Disord. 2008 Mar 15;23(4):588-92. doi: 10.1002/mds.21785. Mov Disord. 2008. PMID: 18175340

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