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Results: 1 to 20 of 92

1.

Challenges in the design and conduct of therapeutic trials in channel disorders.

Venance SL, Herr BE, Griggs RC.

Neurotherapeutics. 2007 Apr;4(2):199-204. Review.

PMID:
17395129
[PubMed - indexed for MEDLINE]
2.

Familial Episodic Ataxias and Related Ion Channel Disorders.

Jen J.

Curr Treat Options Neurol. 2000 Sep;2(5):429-431.

PMID:
11096768
[PubMed - as supplied by publisher]
3.

The primary periodic paralyses: diagnosis, pathogenesis and treatment.

Venance SL, Cannon SC, Fialho D, Fontaine B, Hanna MG, Ptacek LJ, Tristani-Firouzi M, Tawil R, Griggs RC; CINCH investigators.

Brain. 2006 Jan;129(Pt 1):8-17. Epub 2005 Sep 29. Review.

PMID:
16195244
[PubMed - indexed for MEDLINE]
Free Article
4.

Muscle channelopathies: the nondystrophic myotonias and periodic paralyses.

Statland JM, Barohn RJ.

Continuum (Minneap Minn). 2013 Dec;19(6 Muscle Disease):1598-614. doi: 10.1212/01.CON.0000440661.49298.c8. Review.

PMID:
24305449
[PubMed - indexed for MEDLINE]
5.

Calcium channelopathies in inherited neurological disorders: relevance to drug screening for acquired channel disorders.

Lory P, Mezghrani A.

IDrugs. 2010 Jul;13(7):467-71. Review.

PMID:
20582871
[PubMed - indexed for MEDLINE]
6.

Skeletal muscle channelopathies: new insights into the periodic paralyses and nondystrophic myotonias.

Platt D, Griggs R.

Curr Opin Neurol. 2009 Oct;22(5):524-31. doi: 10.1097/WCO.0b013e32832efa8f. Review.

PMID:
19571750
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Episodic ataxia and channelopathies.

Gordon N.

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

PMID:
9533553
[PubMed - indexed for MEDLINE]
8.

State of the art in hereditary muscle channelopathies.

Jurkat-Rott K, Lehmann-Horn F.

Acta Myol. 2010 Oct;29(2):343-50.

PMID:
21314017
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Treatment of neuromuscular channelopathies: current concepts and future prospects.

Cleland JC, Griggs RC.

Neurotherapeutics. 2008 Oct;5(4):607-12. doi: 10.1016/j.nurt.2008.09.001. Review.

PMID:
19019313
[PubMed - indexed for MEDLINE]
10.

[Channelopathies: a genetic explanation of migraine and other paroxysmal neurologic disorders].

Terwindt GM, Ophoff RA, Haan J, Frants RR, Ferrari MD.

Ned Tijdschr Geneeskd. 1998 May 2;142(18):1015-9. Review. Dutch.

PMID:
9623202
[PubMed - indexed for MEDLINE]
11.

Genetic neurological channelopathies.

Hanna MG.

Nat Clin Pract Neurol. 2006 May;2(5):252-63. Review.

PMID:
16932562
[PubMed - indexed for MEDLINE]
12.

Channelopathies: episodic disorders of the nervous system.

Ptacek L.

Novartis Found Symp. 2002;241:87-104; discussion 104-8, 226-32. Review.

PMID:
11771653
[PubMed - indexed for MEDLINE]
13.

Muscle channelopathies.

Saperstein DS.

Semin Neurol. 2008 Apr;28(2):260-9. doi: 10.1055/s-2008-1062262. Review.

PMID:
18351527
[PubMed - indexed for MEDLINE]
14.

Clinical evaluation of membrane excitability in muscle channel disorders: potential applications in clinical trials.

Cleland JC, Logigian EL.

Neurotherapeutics. 2007 Apr;4(2):205-15. Review.

PMID:
17395130
[PubMed - indexed for MEDLINE]
15.

[Channelopathy].

Okamoto K, Ikeda Y.

Rinsho Shinkeigaku. 2001 Dec;41(12):1226-8. Review. Japanese.

PMID:
12235844
[PubMed - indexed for MEDLINE]
16.

Paroxysmal muscle weakness: the familial periodic paralyses.

Jurkat-Rott K, Lehmann-Horn F.

J Neurol. 2006 Nov;253(11):1391-8. Epub 2006 Nov 30. Review.

PMID:
17139526
[PubMed - indexed for MEDLINE]
17.

The nondystrophic myotonias.

Heatwole CR, Moxley RT 3rd.

Neurotherapeutics. 2007 Apr;4(2):238-51. Review.

PMID:
17395134
[PubMed - indexed for MEDLINE]
18.

Episodic neurological channelopathies.

Ryan DP, Ptácek LJ.

Neuron. 2010 Oct 21;68(2):282-92. doi: 10.1016/j.neuron.2010.10.008. Review.

PMID:
20955935
[PubMed - indexed for MEDLINE]
Free Article
19.

Late onset hereditary episodic ataxia.

Damak M, Riant F, Boukobza M, Tournier-Lasserve E, Bousser MG, Vahedi K.

J Neurol Neurosurg Psychiatry. 2009 May;80(5):566-8. doi: 10.1136/jnnp.2008.150615.

PMID:
19372292
[PubMed - indexed for MEDLINE]
20.

Periodic paralysis.

Fontaine B.

Adv Genet. 2008;63:3-23. doi: 10.1016/S0065-2660(08)01001-8. Review.

PMID:
19185183
[PubMed - indexed for MEDLINE]

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