Similar articles for PMID: 15897512

Year	Number of Results
1984	1
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1993	3
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1997	7
1998	6
1999	11
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2009	6
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2017	7
2018	5
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2024	0

1

Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new family.

Kabakci K, Isbruch K, Schilling K, Hedrich K, de Carvalho Aguiar P, Ozelius LJ, Kramer PL, Schwarz MH, Klein C. Kabakci K, et al. J Neurol Neurosurg Psychiatry. 2005 Jun;76(6):860-2. doi: 10.1136/jnnp.2004.046730. J Neurol Neurosurg Psychiatry. 2005. PMID: 15897512 Free PMC article.

2

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. Mov Disord. 2004 Dec;19(12):1506-10. doi: 10.1002/mds.20258. Mov Disord. 2004. PMID: 15390049

3

Rapid-onset dystonia-parkinsonism: linkage to chromosome 19q13.

Kramer PL, Mineta M, Klein C, Schilling K, de Leon D, Farlow MR, Breakefield XO, Bressman SB, Dobyns WB, Ozelius LJ, Brashear A. Kramer PL, et al. Ann Neurol. 1999 Aug;46(2):176-82. doi: 10.1002/1531-8249(199908)46:2<176::aid-ana6>3.0.co;2-2. Ann Neurol. 1999. PMID: 10443882

4

[A childhood-onset rapid-onset dystonia parkinsonism family with ATP1A3 gene mutation and literatures review].

Zhang CL, Yin F, He F, Gai N, Shi ZQ, Peng J. Zhang CL, et al. Zhonghua Er Ke Za Zhi. 2017 Apr 2;55(4):288-293. doi: 10.3760/cma.j.issn.0578-1310.2017.04.011. Zhonghua Er Ke Za Zhi. 2017. PMID: 28441826 Review. Chinese.

5

[Rapid-onset dystonia-parkinsonism].

Zaremba J. Zaremba J. Przegl Lek. 2005;62(11):1296-7. Przegl Lek. 2005. PMID: 16512624 Review. Polish.

6

Rapid-onset dystonia-parkinsonism.

Dobyns WB, Ozelius LJ, Kramer PL, Brashear A, Farlow MR, Perry TR, Walsh LE, Kasarskis EJ, Butler IJ, Breakefield XO. Dobyns WB, et al. Neurology. 1993 Dec;43(12):2596-602. doi: 10.1212/wnl.43.12.2596. Neurology. 1993. PMID: 8255463

7

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. Brain. 2007 Mar;130(Pt 3):828-35. doi: 10.1093/brain/awl340. Epub 2007 Feb 4. Brain. 2007. PMID: 17282997

8

Rapid-onset dystonia-parkinsonism: a clinical and genetic analysis of a new kindred.

Pittock SJ, Joyce C, O'Keane V, Hugle B, Hardiman MO, Brett F, Green AJ, Barton DE, King MD, Webb DW. Pittock SJ, et al. Neurology. 2000 Oct 10;55(7):991-5. doi: 10.1212/wnl.55.7.991. Neurology. 2000. PMID: 11061257

9

The Expanding Phenotypic Spectrums Associated with ATP1A3 Mutation in a Family with Rapid-Onset Dystonia Parkinsonism.

Yuan Y, Ran L, Lei L, Zhu H, Zhu X, Chen H. Yuan Y, et al. Neurodegener Dis. 2020;20(2-3):84-89. doi: 10.1159/000511733. Epub 2020 Dec 16. Neurodegener Dis. 2020. PMID: 33326973

10

Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study.

Djarmati A, Schneider SA, Lohmann K, Winkler S, Pawlack H, Hagenah J, Brüggemann N, Zittel S, Fuchs T, Raković A, Schmidt A, Jabusch HC, Wilcox R, Kostić VS, Siebner H, Altenmüller E, Münchau A, Ozelius LJ, Klein C. Djarmati A, et al. Lancet Neurol. 2009 May;8(5):447-52. doi: 10.1016/S1474-4422(09)70083-3. Epub 2009 Apr 1. Lancet Neurol. 2009. PMID: 19345148

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