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Items: 1 to 20 of 22

1.

PRRT2 mutation correlated with phenotype of paroxysmal kinesigenic dyskinesia and drug response.

Li HF, Chen WJ, Ni W, Wang KY, Liu GL, Wang N, Xiong ZQ, Xu J, Wu ZY.

Neurology. 2013 Apr 16;80(16):1534-5. doi: 10.1212/WNL.0b013e31828cf7e1. Epub 2013 Mar 27. No abstract available.

PMID:
23535490
2.

PRRT2-related disorders: further PKD and ICCA cases and review of the literature.

Becker F, Schubert J, Striano P, Anttonen AK, Liukkonen E, Gaily E, Gerloff C, Müller S, Heußinger N, Kellinghaus C, Robbiano A, Polvi A, Zittel S, von Oertzen TJ, Rostasy K, Schöls L, Warner T, Münchau A, Lehesjoki AE, Zara F, Lerche H, Weber YG.

J Neurol. 2013 May;260(5):1234-44. doi: 10.1007/s00415-012-6777-y. Epub 2013 Jan 9. Review.

PMID:
23299620
3.

PRRT2 mutations and paroxysmal disorders.

Méneret A, Gaudebout C, Riant F, Vidailhet M, Depienne C, Roze E.

Eur J Neurol. 2013 Jun;20(6):872-8. doi: 10.1111/ene.12104. Epub 2013 Feb 9. Review.

PMID:
23398397
4.

Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.

Erro R, Sheerin UM, Bhatia KP.

Mov Disord. 2014 Aug;29(9):1108-16. doi: 10.1002/mds.25933. Epub 2014 Jun 25. Review.

PMID:
24963779
5.

Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy.

Heron SE, Dibbens LM.

J Med Genet. 2013 Mar;50(3):133-9. doi: 10.1136/jmedgenet-2012-101406. Epub 2013 Jan 23. Review.

PMID:
23343561
6.

Treatment of paroxysmal dyskinesias.

Strzelczyk A, Bürk K, Oertel WH.

Expert Opin Pharmacother. 2011 Jan;12(1):63-72. doi: 10.1517/14656566.2010.513971. Epub 2010 Nov 26. Review.

PMID:
21108579
7.

Episodic movement disorders: from phenotype to genotype and back.

Brockmann K.

Curr Neurol Neurosci Rep. 2013 Oct;13(10):379. doi: 10.1007/s11910-013-0379-7. Review.

PMID:
23963607
8.

[Paroxysmal dyskinesias].

Perona-Moratalla AB, Argandoña L, García-Muñozguren S.

Rev Neurol. 2009 Jan 23;48 Suppl 1:S7-9. Review. Spanish.

9.

Familial (idiopathic) paroxysmal dyskinesias: an update.

Bhatia KP.

Semin Neurol. 2001;21(1):69-74. Review.

PMID:
11346027
10.

Paroxysmal dyskinesias as a paradigm of paroxysmal movement disorders.

Vidailhet M.

Curr Opin Neurol. 2000 Aug;13(4):457-62. Review.

PMID:
10970065
11.

Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.

Houser MK, Soland VL, Bhatia KP, Quinn NP, Marsden CD.

J Neurol. 1999 Feb;246(2):120-6. Review.

PMID:
10195407
12.

Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria.

Bruno MK, Hallett M, Gwinn-Hardy K, Sorensen B, Considine E, Tucker S, Lynch DR, Mathews KD, Swoboda KJ, Harris J, Soong BW, Ashizawa T, Jankovic J, Renner D, Fu YH, Ptacek LJ.

Neurology. 2004 Dec 28;63(12):2280-7. Review.

PMID:
15623687
13.

[Non-epileptic paroxysmal movement disorders].

Klein C, Vieregge P.

Nervenarzt. 1998 Aug;69(8):647-59. Review. German.

PMID:
9757415
14.

Paroxysmal kinesigenic dyskinesias.

Lotze T, Jankovic J.

Semin Pediatr Neurol. 2003 Mar;10(1):68-79. Review.

PMID:
12785750
15.

The paroxysmal dyskinesias.

Bhatia KP.

J Neurol. 1999 Mar;246(3):149-55. Review.

PMID:
10323309
16.

[Recent advances of genetic research on paroxysmal kinesigenic dyskinesias].

Li XH, Chen SQ, Wang YM.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Aug;25(4):410-3. Review. Chinese.

PMID:
18683138
17.

Autosomal dominant paroxysmal kinesigenic choreoathetosis. An electroneurophysiological study.

Busard HL, Renier WO, Gabreëls FJ, Vos AJ, Declerck AC, Verhey FH.

Clin Neurol Neurosurg. 1984;86(4):281-9. Review.

PMID:
6096061
18.

[Paroxysmal kinesigenic choreoathetosis].

Ueki A.

Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):326-9. Review. Japanese. No abstract available.

PMID:
12483893
19.

Diagnosis and management of acute movement disorders.

Dressler D, Benecke R.

J Neurol. 2005 Nov;252(11):1299-306. Epub 2005 Oct 10. Review.

PMID:
16208529
20.

The genetics of dystonia: new twists in an old tale.

Charlesworth G, Bhatia KP, Wood NW.

Brain. 2013 Jul;136(Pt 7):2017-37. doi: 10.1093/brain/awt138. Epub 2013 Jun 17. Review.

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