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Results: 1 to 20 of 161

Similar articles for PubMed (Select 21891927)

1.

Expression patterns of two potassium channel genes in skeletal muscle cells of patients with familial hypokalemic periodic paralysis.

Kim JB, Lee GM, Kim SJ, Yoon DH, Lee YH.

Neurol India. 2011 Jul-Aug;59(4):527-31. doi: 10.4103/0028-3886.84331.

2.

Reduced expression and abnormal localization of the K(ATP) channel subunit SUR2A in patients with familial hypokalemic periodic paralysis.

Kim SJ, Lee YJ, Kim JB.

Biochem Biophys Res Commun. 2010 Jan 1;391(1):974-8. doi: 10.1016/j.bbrc.2009.11.177. Epub 2009 Dec 4.

PMID:
19962959
3.

The large-conductance calcium-activated potassium channel holds the key to the conundrum of familial hypokalemic periodic paralysis.

Kim JB, Kim SJ, Kang SY, Yi JW, Kim SM.

Korean J Pediatr. 2014 Oct;57(10):445-50. doi: 10.3345/kjp.2014.57.10.445. Epub 2014 Oct 31.

4.
5.

Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current.

Jurkat-Rott K, Mitrovic N, Hang C, Kouzmekine A, Iaizzo P, Herzog J, Lerche H, Nicole S, Vale-Santos J, Chauveau D, Fontaine B, Lehmann-Horn F.

Proc Natl Acad Sci U S A. 2000 Aug 15;97(17):9549-54.

6.

Mutation screening in Chinese hypokalemic periodic paralysis patients.

Wang W, Jiang L, Ye L, Zhu N, Su T, Guan L, Li X, Ning G.

Mol Genet Metab. 2006 Apr;87(4):359-63. Epub 2006 Jan 4.

PMID:
16386935
7.

Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis.

Ryan DP, da Silva MR, Soong TW, Fontaine B, Donaldson MR, Kung AW, Jongjaroenprasert W, Liang MC, Khoo DH, Cheah JS, Ho SC, Bernstein HS, Maciel RM, Brown RH Jr, Ptácek LJ.

Cell. 2010 Jan 8;140(1):88-98. doi: 10.1016/j.cell.2009.12.024.

8.
9.

A patient suffering from hypokalemic periodic paralysis is deficient in skeletal muscle ATP-sensitive K channels.

Jovanović S, Du Q, Mukhopadhyay S, Swingler R, Buckley R, McEachen J, Jovanović A.

Clin Transl Sci. 2008 May;1(1):71-4. doi: 10.1111/j.1752-8062.2008.00007.x.

10.

Periodic paralysis.

Fontaine B.

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

PMID:
19185183
11.

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.

12.

The genotype and clinical phenotype of Korean patients with familial hypokalemic periodic paralysis.

Kim JB, Kim MH, Lee SJ, Kim DJ, Lee BC.

J Korean Med Sci. 2007 Dec;22(6):946-51.

13.

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.

Ke T, Gomez CR, Mateus HE, Castano JA, Wang QK.

J Hum Genet. 2009 Nov;54(11):660-4. doi: 10.1038/jhg.2009.92. Epub 2009 Sep 25.

PMID:
19779499
14.

Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.

Sternberg D, Maisonobe T, Jurkat-Rott K, Nicole S, Launay E, Chauveau D, Tabti N, Lehmann-Horn F, Hainque B, Fontaine B.

Brain. 2001 Jun;124(Pt 6):1091-9.

15.

[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
16.
17.
18.

[Current status of clinical and molecular-biological research on familial periodic paralysis].

Shishiba Y.

Nihon Rinsho. 1997 Dec;55(12):3239-46. Review. Japanese.

PMID:
9436444
19.

Hypokalemic periodic paralysis due to the SCN4A R672H mutation in a Turkish family.

Incecik F, Hergüner MO, Altunbaşak S, Lehman-Horn F.

Turk J Pediatr. 2010 Jul-Aug;52(4):409-10.

20.

Molecular basis for hyperkalemic periodic paralysis.

Brown RH Jr.

Int J Neurol. 1991-1992;25-26:89-96. Review.

PMID:
11980067
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