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Items: 1 to 20 of 246

1.

Normokalemic periodic paralysis revisited: does it exist?

Chinnery PF, Walls TJ, Hanna MG, Bates D, Fawcett PR.

Ann Neurol. 2002 Aug;52(2):251-2.

PMID:
12210802
2.

[Screening SCN4A gene for mutations with denaturing high performance liquid chromatography technology in a Chinese family with normokalemic periodic paralysis].

Guo XH, Wu WP, Zhang YH, Wang HB, Mao YL, Zhu K.

Zhonghua Yi Xue Za Zhi. 2004 Jan 17;84(2):125-9. Chinese.

PMID:
14990128
3.

Normokalemic periodic paralysis is not a distinct disease.

Song YW, Kim SJ, Heo TH, Kim MH, Kim JB.

Muscle Nerve. 2012 Dec;46(6):914-6. doi: 10.1002/mus.23441. Epub 2012 Aug 24.

PMID:
22926674
4.

[The mutation V781I in SCN4A gene exists in Chinese patients with normokalemic periodic paralysis].

Guo XH, Wu WP, Zhang YH, Jia JP, Zhu K.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):566-9. Chinese.

PMID:
15583983
5.

Exercise test on the patients with normokalaemic periodic paralysis from a Chinese family with a mutation in the SCN4A gene.

Feng Y, Zhang Y, Liu ZL, Zhang CD.

Chin Med J (Engl). 2008 Oct 5;121(19):1915-9.

PMID:
19080124
6.
7.

[Clinical and molecular genetic analysis of a family with normokalemic periodic paralysis].

Wei CJ, Wang D, Wang S, Jiao H, Hong DJ, Pu LH, Xiong H.

Zhonghua Er Ke Za Zhi. 2013 Jan;51(1):47-51. Chinese.

PMID:
23527931
8.

New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis.

Vicart S, Sternberg D, Fournier E, Ochsner F, Laforet P, Kuntzer T, Eymard B, Hainque B, Fontaine B.

Neurology. 2004 Dec 14;63(11):2120-7.

PMID:
15596759
9.

Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations.

Plassart E, Reboul J, Rime CS, Recan D, Millasseau P, Eymard B, Pelletier J, Thomas C, Chapon F, Desnuelle C, et al.

Eur J Hum Genet. 1994;2(2):110-24.

PMID:
8044656
10.

Mutations of sodium channel alpha-subunit genes in Chinese patients with normokalemic periodic paralysis.

Xiuhai G, Weiping W, Ke Z, Hongbin W, Yiling S, MaoYanling.

Cell Mol Neurobiol. 2008 Aug;28(5):653-61. Epub 2007 Nov 29.

PMID:
18046642
11.

Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene.

Ebers GC, George AL, Barchi RL, Ting-Passador SS, Kallen RG, Lathrop GM, Beckmann JS, Hahn AF, Brown WF, Campbell RD, et al.

Ann Neurol. 1991 Dec;30(6):810-6.

PMID:
1686388
12.

Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis.

Ptáĉek LJ, Tawil R, Griggs RC, Meola G, McManis P, Barohn RJ, Mendell JR, Harris C, Spitzer R, Santiago F, et al.

Neurology. 1994 Aug;44(8):1500-3.

PMID:
8058156
13.

Hyperkalemic periodic paralysis: rapid molecular diagnosis and relationship of genotype to phenotype in 12 families.

Feero WG, Wang J, Barany F, Zhou J, Todorovic SM, Conwit R, Galloway G, Hausmanowa-Petrusewicz I, Fidzianska A, Arahata K, et al.

Neurology. 1993 Apr;43(4):668-73.

PMID:
8385748
14.

Identification of a mutation in the gene causing hyperkalemic periodic paralysis.

Ptácek LJ, George AL Jr, Griggs RC, Tawil R, Kallen RG, Barchi RL, Robertson M, Leppert MF.

Cell. 1991 Nov 29;67(5):1021-7.

PMID:
1659948
15.

Periodic paralysis.

Fontaine B.

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

PMID:
19185183
16.
17.

Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis.

Sternberg D, Tabti N, Fournier E, Hainque B, Fontaine B.

Neurology. 2003 Sep 23;61(6):857-9.

PMID:
14504341
18.

Hyperkalemic periodic paralysis with cardiac dysrhythmia: a novel sodium channel mutation?

Baquero JL, Ayala RA, Wang J, Curless RG, Feero WG, Hoffman EP, Ebeid MR.

Ann Neurol. 1995 Mar;37(3):408-11.

PMID:
7695243
19.
20.

Possible normokalemic variant of hyperkalemic periodic paralysis in two horses.

Stewart RH, Bertone JJ, Yvorchuk-St Jean K, Reed SM, Neil WH Jr.

J Am Vet Med Assoc. 1993 Aug 1;203(3):421-4.

PMID:
8226220

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