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Items: 1 to 20 of 45

1.

The clinical and genetic heterogeneity of paroxysmal dyskinesias.

Gardiner AR, Jaffer F, Dale RC, Labrum R, Erro R, Meyer E, Xiromerisiou G, Stamelou M, Walker M, Kullmann D, Warner T, Jarman P, Hanna M, Kurian MA, Bhatia KP, Houlden H.

Brain. 2015 Dec;138(Pt 12):3567-80. doi: 10.1093/brain/awv310. Epub 2015 Nov 23. Review.

2.

The evolving spectrum of PRRT2-associated paroxysmal diseases.

Ebrahimi-Fakhari D, Saffari A, Westenberger A, Klein C.

Brain. 2015 Dec;138(Pt 12):3476-95. doi: 10.1093/brain/awv317. Epub 2015 Nov 23. Review.

PMID:
26598493
3.

Paroxysmal movement disorders.

Waln O, Jankovic J.

Neurol Clin. 2015 Feb;33(1):137-52. doi: 10.1016/j.ncl.2014.09.014. Review.

PMID:
25432727
4.

[PRRT2 gene-related paroxysmal disorders].

Li J, Mao X, Wang J, Li N, Tang B.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Oct;31(5):595-9. doi: 10.3760/cma.j.issn.1003-9406.2014.01.012. Review. Chinese.

PMID:
25297589
5.

A case of familial paroxysmal nonkinesigenic dyskinesia due to mutation of the PNKD gene in Chinese Mainland.

Liang S, Yu X, Zhang S, Tai J.

Brain Res. 2015 Jan 21;1595:120-6. doi: 10.1016/j.brainres.2014.07.047. Epub 2014 Aug 5. Review.

PMID:
25107857
6.

GLUT1 deficiency syndrome 2013: current state of the art.

De Giorgis V, Veggiotti P.

Seizure. 2013 Dec;22(10):803-11. doi: 10.1016/j.seizure.2013.07.003. Epub 2013 Jul 26. Review.

7.

Paroxysmal movement disorders and episodic ataxias.

Fernández-Alvarez E, Perez-Dueñas B.

Handb Clin Neurol. 2013;112:847-52. doi: 10.1016/B978-0-444-52910-7.00004-0. Review.

PMID:
23622292
8.

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
9.

[Paroxysmal dyskinesias].

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

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

10.

Genetics of infantile seizures with paroxysmal dyskinesia: the infantile convulsions and choreoathetosis (ICCA) and ICCA-related syndromes.

Rochette J, Roll P, Szepetowski P.

J Med Genet. 2008 Dec;45(12):773-9. doi: 10.1136/jmg.2008.059519. Review.

PMID:
19047496
11.

[Glucose transporter type 1 (GLUT-1) deficiency].

Cano A, Ticus I, Chabrol B.

Rev Neurol (Paris). 2008 Nov;164(11):896-901. doi: 10.1016/j.neurol.2008.02.033. Epub 2008 Apr 3. Review. French.

PMID:
18808765
12.

[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
13.

Paroxysmal kinesigenic choreoathetosis: from first discovery in 1892 to genetic linkage with benign familial infantile convulsions.

Kato N, Sadamatsu M, Kikuchi T, Niikawa N, Fukuyama Y.

Epilepsy Res. 2006 Aug;70 Suppl 1:S174-84. Epub 2006 Aug 9. Review.

PMID:
16901678
14.

Benign partial epilepsy in infancy long-term outcome and marginal syndromes.

Okumura A, Watanabe K, Negoro T.

Epilepsy Res. 2006 Aug;70 Suppl 1:S168-73. Epub 2006 Jul 11. Review.

PMID:
16837166
15.

Benign familial infantile seizures.

Vigevano F.

Brain Dev. 2005 Apr;27(3):172-7. Review.

PMID:
15737697
16.

Paroxysmal kinesigenic dyskinesias.

Lotze T, Jankovic J.

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

PMID:
12785750
17.

Deep brain stimulation for dystonia in adults. Overview and developments.

Krauss JK.

Stereotact Funct Neurosurg. 2002;78(3-4):168-82. Review.

PMID:
12652041
18.

[Paroxysmal dystonic choreoathetosis].

Ueki A.

Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):330-2. Review. Japanese. No abstract available.

PMID:
12483894
19.

[Paroxysmal kinesigenic choreoathetosis].

Ueki A.

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

PMID:
12483893
20.

Inherited movement disorders.

Sharma N, Standaert DG.

Neurol Clin. 2002 Aug;20(3):759-78, vii. Review.

PMID:
12432829

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