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Items: 13

1.

DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA.

Camargos S, Scholz S, Simón-Sánchez J, Paisán-Ruiz C, Lewis P, Hernandez D, Ding J, Gibbs JR, Cookson MR, Bras J, Guerreiro R, Oliveira CR, Lees A, Hardy J, Cardoso F, Singleton AB.

Lancet Neurol. 2008 Mar;7(3):207-15. doi: 10.1016/S1474-4422(08)70022-X. Epub 2008 Feb 1.

PMID:
18243799
2.

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
3.

Early onset primary dystonia.

Zorzi G, Zibordi F, Garavaglia B, Nardocci N.

Eur J Paediatr Neurol. 2009 Nov;13(6):488-92. doi: 10.1016/j.ejpn.2008.12.001. Epub 2009 Jan 20. Review.

PMID:
19157930
4.

X-linked recessive dystonia parkinsonism (XDP; Lubag; DYT3).

Singleton A, Hague S, Hernandez D.

Adv Neurol. 2004;94:139-42. Review. No abstract available.

PMID:
14509666
5.

[Rapid-onset dystonia-parkinsonism].

Zaremba J.

Przegl Lek. 2005;62(11):1296-7. Review. Polish.

PMID:
16512624
6.

Sex linked recessive dystonia parkinsonism of Panay, Philippines (XDP).

Lee LV, Munoz EL, Tan KT, Reyes MT.

Mol Pathol. 2001 Dec;54(6):362-8. Review.

7.

Complicated recessive dystonia parkinsonism syndromes.

Schneider SA, Bhatia KP, Hardy J.

Mov Disord. 2009 Mar 15;24(4):490-9. doi: 10.1002/mds.22314. Review.

PMID:
19185014
8.

Rare causes of dystonia parkinsonism.

Schneider SA, Bhatia KP.

Curr Neurol Neurosci Rep. 2010 Nov;10(6):431-9. doi: 10.1007/s11910-010-0136-0. Review.

PMID:
20694531
9.

The monogenic primary dystonias.

Müller U.

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

10.

The natural history of sex-linked recessive dystonia parkinsonism of Panay, Philippines (XDP).

Lee LV, Maranon E, Demaisip C, Peralta O, Borres-Icasiano R, Arancillo J, Rivera C, Munoz E, Tan K, Reyes MT.

Parkinsonism Relat Disord. 2002 Oct;9(1):29-38. Review.

PMID:
12217620
11.

Genetics and treatment of dystonia.

Schwarz CS, Bressman SB.

Neurol Clin. 2009 Aug;27(3):697-718, vi. doi: 10.1016/j.ncl.2009.04.010. Review.

PMID:
19555827
12.

DYT2 revealed: Hippocalcin mutations cause autosomal-recessive isolated dystonia.

Erro R, Klein C.

Mov Disord. 2015 Nov;30(13):1725. doi: 10.1002/mds.26280. Epub 2015 Jun 12. Review. No abstract available.

PMID:
26094611
13.

Dystonia in children and adolescents: a systematic review and a new diagnostic algorithm.

van Egmond ME, Kuiper A, Eggink H, Sinke RJ, Brouwer OF, Verschuuren-Bemelmans CC, Sival DA, Tijssen MA, de Koning TJ.

J Neurol Neurosurg Psychiatry. 2015 Jul;86(7):774-81. doi: 10.1136/jnnp-2014-309106. Epub 2014 Nov 13. Review.

PMID:
25395479
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