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Items: 16

1.

A calcium channel mutant mouse model of hypokalemic periodic paralysis.

Wu F, Mi W, Hernández-Ochoa EO, Burns DK, Fu Y, Gray HF, Struyk AF, Schneider MF, Cannon SC.

J Clin Invest. 2012 Dec;122(12):4580-91. doi: 10.1172/JCI66091. Epub 2012 Nov 26.

2.

Voltage-sensor mutations in channelopathies of skeletal muscle.

Cannon SC.

J Physiol. 2010 Jun 1;588(Pt 11):1887-95. doi: 10.1113/jphysiol.2010.186874. Epub 2010 Feb 15. Review.

3.

Muscle channelopathies: does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis?

Matthews E, Hanna MG.

J Physiol. 2010 Jun 1;588(Pt 11):1879-86. doi: 10.1113/jphysiol.2009.186627. Epub 2010 Feb 1. Review.

4.
5.

Periodic paralysis: understanding channelopathies.

Lehmann-Horn F, Jurkat-Rott K, Rüdel R.

Curr Neurol Neurosci Rep. 2002 Jan;2(1):61-9. Review.

PMID:
11898585
6.

[From gene to diseases; hypokalemic periodic paralysis].

Links TP, Ginjaar HB, van der Hoeven JH.

Ned Tijdschr Geneeskd. 2004 May 22;148(21):1035-8. Review. Dutch.

PMID:
15185439
7.

Extracellular potassium homeostasis: insights from hypokalemic periodic paralysis.

Cheng CJ, Kuo E, Huang CL.

Semin Nephrol. 2013 May;33(3):237-47. doi: 10.1016/j.semnephrol.2013.04.004. Review.

8.
9.

Hallmarks of the channelopathies associated with L-type calcium channels: a focus on the Timothy mutations in Ca(v)1.2 channels.

Bidaud I, Lory P.

Biochimie. 2011 Dec;93(12):2080-6. doi: 10.1016/j.biochi.2011.05.015. Epub 2011 May 31. Review.

PMID:
21664226
10.

Periodic paralysis.

Fontaine B.

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

PMID:
19185183
11.

Treatment for periodic paralysis.

Sansone V, Meola G, Links TP, Panzeri M, Rose MR.

Cochrane Database Syst Rev. 2008 Jan 23;(1):CD005045. doi: 10.1002/14651858.CD005045.pub2. Review.

PMID:
18254068
12.

L-type Ca2+ channels in Ca2+ channelopathies.

Striessnig J, Hoda JC, Koschak A, Zaghetto F, Müllner C, Sinnegger-Brauns MJ, Wild C, Watschinger K, Trockenbacher A, Pelster G.

Biochem Biophys Res Commun. 2004 Oct 1;322(4):1341-6. Review.

PMID:
15336981
13.

Mechanism of thyrotoxic periodic paralysis.

Lin SH, Huang CL.

J Am Soc Nephrol. 2012 Jun;23(6):985-8. doi: 10.1681/ASN.2012010046. Epub 2012 Mar 29. Review.

14.

Channelopathies of skeletal muscle excitability.

Cannon SC.

Compr Physiol. 2015 Apr;5(2):761-90. doi: 10.1002/cphy.c140062. Review.

15.

Ca(V)1.1: The atypical prototypical voltage-gated Ca²⁺ channel.

Bannister RA, Beam KG.

Biochim Biophys Acta. 2013 Jul;1828(7):1587-97. doi: 10.1016/j.bbamem.2012.09.007. Epub 2012 Sep 13. Review.

16.

Disease-causing mutations or functional polymorphisms?

Lehmann-Horn F.

Acta Myol. 2004 Sep;23(2):85-9. Review.

PMID:
15605949

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