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Items: 1 to 20 of 71

1.

News on ion channels: erythromelalgia, treatment of episodic ataxia and faciobrachial dystonic seizures.

Strupp M.

J Neurol. 2011 Sep;258(9):1734-6. doi: 10.1007/s00415-011-6215-6. No abstract available.

PMID:
21847615
2.

Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures.

Jen JC, Wan J, Palos TP, Howard BD, Baloh RW.

Neurology. 2005 Aug 23;65(4):529-34.

PMID:
16116111
3.

Faciobrachial dystonic attacks: seizures or movement disorder?

Striano P.

Ann Neurol. 2011 Jul;70(1):179-80; author reply 180. doi: 10.1002/ana.22470. No abstract available.

PMID:
21786308
4.

Faciobrachial dystonic seizures associated with Hashimoto encephalopathy.

Tsai MH, Cheng MY, Fu TY, Chuang YC.

Eur J Neurol. 2015 Jul;22(7):e72-4. doi: 10.1111/ene.12681. No abstract available.

PMID:
26060928
5.
6.

Episodic ataxia/myokymia mutations functionally expressed in the Shaker potassium channel.

Boland LM, Price DL, Jackson KA.

Neuroscience. 1999;91(4):1557-64.

PMID:
10391459
7.

Alternating faciobrachial dystonic seizures in LGI1-antibody limbic encephalitis.

Rodríguez Cruz PM, Pérez Sánchez JR, Alarcón Morcillo C, Velázquez Pérez JM.

Pract Neurol. 2016 Oct;16(5):387-8. doi: 10.1136/practneurol-2016-001375. Epub 2016 Mar 16. No abstract available.

PMID:
26984950
8.

Genetics of familial episodic vertigo and ataxia.

Baloh RW, Jen JC.

Ann N Y Acad Sci. 2002 Apr;956:338-45.

PMID:
11960817
9.

Ion channels and epilepsy.

Armijo JA, Shushtarian M, Valdizan EM, Cuadrado A, de las Cuevas I, Adín J.

Curr Pharm Des. 2005;11(15):1975-2003. Review.

PMID:
15974971
10.

Erythromelalgia: a hereditary pain syndrome enters the molecular era.

Waxman SG, Dib-Hajj SD.

Ann Neurol. 2005 Jun;57(6):785-8.

PMID:
15929046
11.

Episodic ataxia results from voltage-dependent potassium channels with altered functions.

Adelman JP, Bond CT, Pessia M, Maylie J.

Neuron. 1995 Dec;15(6):1449-54.

12.

Episodic ataxia and channelopathies.

Gordon N.

Brain Dev. 1998 Jan;20(1):9-13. Review.

PMID:
9533553
13.

Imaging findings in faciobrachial dystonic seizures associated with LGI-1 antibodies.

Grativvol RS, Simabukuro MM, Spera RR, Cavalcante WC, Araújo HH, Sakuno D, Lucato LT, Pinto LF, Castro LH, Nitrini R.

Arq Neuropsiquiatr. 2016 Nov;74(11):947. doi: 10.1590/0004-282X20160146. No abstract available.

14.

Striking basal ganglia imaging abnormalities in LGI1 ab faciobrachial dystonic seizures.

López Chiriboga AS, Siegel JL, Tatum WO, Shih JJ, Flanagan EP.

Neurol Neuroimmunol Neuroinflamm. 2017 Mar 14;4(3):e336. doi: 10.1212/NXI.0000000000000336. eCollection 2017 May. No abstract available.

15.

Mexiletine-responsive erythromelalgia due to a new Na(v)1.7 mutation showing use-dependent current fall-off.

Choi JS, Zhang L, Dib-Hajj SD, Han C, Tyrrell L, Lin Z, Wang X, Yang Y, Waxman SG.

Exp Neurol. 2009 Apr;216(2):383-9. doi: 10.1016/j.expneurol.2008.12.012. Epub 2008 Dec 31.

PMID:
19162012
16.

Familial episodic ataxia: a model for migrainous vertigo.

Jen JC, Baloh RW.

Ann N Y Acad Sci. 2009 May;1164:252-6. doi: 10.1111/j.1749-6632.2008.03723.x.

PMID:
19645908
17.

L-type calcium channels contribute to the tottering mouse dystonic episodes.

Campbell DB, Hess EJ.

Mol Pharmacol. 1999 Jan;55(1):23-31.

18.

Episodic ataxia type 1 and 2 (familial periodic ataxia/vertigo).

Brandt T, Strupp M.

Audiol Neurootol. 1997 Nov-Dec;2(6):373-83. Review.

PMID:
9390841
19.

Disorders of membrane channels or channelopathies.

Celesia GG.

Clin Neurophysiol. 2001 Jan;112(1):2-18. Review.

PMID:
11137655
20.

Hereditary episodic ataxias.

Jen JC.

Ann N Y Acad Sci. 2008 Oct;1142:250-3. doi: 10.1196/annals.1444.016. Review.

PMID:
18990130

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