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Items: 1 to 20 of 117

1.

Alternative approaches to modeling hereditary dystonias.

Fremont R, Khodakhah K.

Neurotherapeutics. 2012 Apr;9(2):315-22. doi: 10.1007/s13311-012-0113-1. Review.

2.

Aberrant Purkinje cell activity is the cause of dystonia in a shRNA-based mouse model of Rapid Onset Dystonia-Parkinsonism.

Fremont R, Tewari A, Khodakhah K.

Neurobiol Dis. 2015 Oct;82:200-212. doi: 10.1016/j.nbd.2015.06.004. Epub 2015 Jun 17.

3.

Abnormal high-frequency burst firing of cerebellar neurons in rapid-onset dystonia-parkinsonism.

Fremont R, Calderon DP, Maleki S, Khodakhah K.

J Neurosci. 2014 Aug 27;34(35):11723-32. doi: 10.1523/JNEUROSCI.1409-14.2014.

4.

The neural substrates of rapid-onset Dystonia-Parkinsonism.

Calderon DP, Fremont R, Kraenzlin F, Khodakhah K.

Nat Neurosci. 2011 Mar;14(3):357-65. doi: 10.1038/nn.2753. Epub 2011 Feb 6.

5.

Heterozygous mice deficient in Atp1a3 exhibit motor deficits by chronic restraint stress.

Sugimoto H, Ikeda K, Kawakami K.

Behav Brain Res. 2014 Oct 1;272:100-10. doi: 10.1016/j.bbr.2014.06.048. Epub 2014 Jun 29.

PMID:
24983657
6.

The basal ganglia and cerebellum interact in the expression of dystonic movement.

Neychev VK, Fan X, Mitev VI, Hess EJ, Jinnah HA.

Brain. 2008 Sep;131(Pt 9):2499-509. doi: 10.1093/brain/awn168. Epub 2008 Jul 26.

7.

Engineering animal models of dystonia.

Oleas J, Yokoi F, DeAndrade MP, Pisani A, Li Y.

Mov Disord. 2013 Jun 15;28(7):990-1000. doi: 10.1002/mds.25583. Review.

8.

The monogenic primary dystonias.

Müller U.

Brain. 2009 Aug;132(Pt 8):2005-25. doi: 10.1093/brain/awp172. Epub 2009 Jul 3. Review.

PMID:
19578124
9.

[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.

Zhonghua Er Ke Za Zhi. 2017 Apr 2;55(4):288-293. doi: 10.3760/cma.j.issn.0578-1310.2017.04.011. Review. Chinese.

PMID:
28441826
10.

Primary dystonias and genetic disorders with dystonia as clinical feature of the disease.

Moghimi N, Jabbari B, Szekely AM.

Eur J Paediatr Neurol. 2014 Jan;18(1):79-105. doi: 10.1016/j.ejpn.2013.05.015. Epub 2013 Jul 30. Review.

PMID:
23911094
11.

Chapter 33: the history of movement disorders.

Lanska DJ.

Handb Clin Neurol. 2010;95:501-46. doi: 10.1016/S0072-9752(08)02133-7. Review.

PMID:
19892136
12.

Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.

DeAndrade MP, Yokoi F, van Groen T, Lingrel JB, Li Y.

Behav Brain Res. 2011 Jan 20;216(2):659-65. doi: 10.1016/j.bbr.2010.09.009. Epub 2010 Sep 17.

13.

Progressive dystonia.

Klein C, Münchau A.

Handb Clin Neurol. 2013;113:1889-97. doi: 10.1016/B978-0-444-59565-2.00059-9. Review.

PMID:
23622412
14.

[Primary and secondary dystonias].

Kerty E.

Tidsskr Nor Laegeforen. 2008 Oct 9;128(19):2206-9. Norwegian.

15.

Pathology of idiopathic dystonia: findings from genetic animal models.

Richter A, Löscher W.

Prog Neurobiol. 1998 Apr;54(6):633-77. Review.

PMID:
9560845
16.

[Hereditary dystonias].

Hjermind LE, Sørensen SA, Werdelin LM.

Ugeskr Laeger. 2000 Sep 18;162(38):5066-70. Review. Danish.

PMID:
11014135
17.

Update on the pathology of dystonia.

Standaert DG.

Neurobiol Dis. 2011 May;42(2):148-51. doi: 10.1016/j.nbd.2011.01.012. Epub 2011 Jan 8. Review.

18.
19.

Distribution of Na/K-ATPase alpha 3 isoform, a sodium-potassium P-type pump associated with rapid-onset of dystonia parkinsonism (RDP) in the adult mouse brain.

Bøttger P, Tracz Z, Heuck A, Nissen P, Romero-Ramos M, Lykke-Hartmann K.

J Comp Neurol. 2011 Feb 1;519(2):376-404. doi: 10.1002/cne.22524.

PMID:
21165980
20.

Dystonia-plus syndromes.

Asmus F, Gasser T.

Eur J Neurol. 2010 Jul;17 Suppl 1:37-45. doi: 10.1111/j.1468-1331.2010.03049.x. Review.

PMID:
20590807

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