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Items: 1 to 20 of 329

1.

Andersen's syndrome: a distinct periodic paralysis.

Sansone V, Griggs RC, Meola G, Ptácek LJ, Barohn R, Iannaccone S, Bryan W, Baker N, Janas SJ, Scott W, Ririe D, Tawil R.

Ann Neurol. 1997 Sep;42(3):305-12.

2.

Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features.

Tawil R, Ptacek LJ, Pavlakis SG, DeVivo DC, Penn AS, Ozdemir C, Griggs RC.

Ann Neurol. 1994 Mar;35(3):326-30.

PMID:
8080508
3.

[Andersen syndrome, ventricular arrhythmias and channelopathy (a case report)].

Lucet V, Lupoglazoff JM, Fontaine B.

Arch Pediatr. 2002 Dec;9(12):1256-9. French.

PMID:
12536108
4.

Different gene loci for hyperkalemic and hypokalemic periodic paralysis.

Fontaine B, Trofatter J, Rouleau GA, Khurana TS, Haines J, Brown R, Gusella JF.

Neuromuscul Disord. 1991;1(4):235-8.

PMID:
1822800
5.

In vivo and in vitro functional characterization of Andersen's syndrome mutations.

Bendahhou S, Fournier E, Sternberg D, Bassez G, Furby A, Sereni C, Donaldson MR, Larroque MM, Fontaine B, Barhanin J.

J Physiol. 2005 Jun 15;565(Pt 3):731-41. Epub 2005 Apr 14.

6.

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome.

Plaster NM, Tawil R, Tristani-Firouzi M, Canún S, Bendahhou S, Tsunoda A, Donaldson MR, Iannaccone ST, Brunt E, Barohn R, Clark J, Deymeer F, George AL Jr, Fish FA, Hahn A, Nitu A, Ozdemir C, Serdaroglu P, Subramony SH, Wolfe G, Fu YH, Ptácek LJ.

Cell. 2001 May 18;105(4):511-9.

7.
8.

Periodic paralysis.

Fontaine B.

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

PMID:
19185183
9.

Primary periodic paralyses.

Finsterer J.

Acta Neurol Scand. 2008 Mar;117(3):145-58. Epub 2007 Nov 20. Review.

PMID:
18031562
10.

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene.

Fontaine B, Khurana TS, Hoffman EP, Bruns GA, Haines JL, Trofatter JA, Hanson MP, Rich J, McFarlane H, Yasek DM, et al.

Science. 1990 Nov 16;250(4983):1000-2.

PMID:
2173143
11.

Progressive myopathy in hyperkalemic periodic paralysis.

Bradley WG, Taylor R, Rice DR, Hausmanowa-Petruzewicz I, Adelman LS, Jenkison M, Jedrzejowska H, Drac H, Pendlebury WW.

Arch Neurol. 1990 Sep;47(9):1013-7.

PMID:
2396930
12.

Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes.

Sacconi S, Simkin D, Arrighi N, Chapon F, Larroque MM, Vicart S, Sternberg D, Fontaine B, Barhanin J, Desnuelle C, Bendahhou S.

Am J Physiol Cell Physiol. 2009 Oct;297(4):C876-85. doi: 10.1152/ajpcell.00519.2008. Epub 2009 Jul 1.

13.

Familial hypokalemic periodic paralysis. 50-year follow-up of a large family.

Buruma OJ, Bots GT, Went LN.

Arch Neurol. 1985 Jan;42(1):28-31.

PMID:
3855357
14.

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
15.

[Periodic hypokalemic paralysis. Report of a case and genealogic study of the family].

Cognazzo A, Grasso E.

Minerva Med. 1973 Oct 3;64(69):3616-9. Italian. No abstract available.

PMID:
4798085
16.

The LQT syndromes--current status of molecular mechanisms.

Schulze-Bahr E, Wedekind H, Haverkamp W, Borggrefe M, Assmann G, Breithardt G, Funke H.

Z Kardiol. 1999 Apr;88(4):245-54. Review.

PMID:
10408028
17.

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
18.
19.

[Periodic paralysis. Clinical analysis in 20 patients].

Tengan CH, De Oliveira AS, Gabbai AA.

Arq Neuropsiquiatr. 1994 Dec;52(4):501-9. Portuguese.

PMID:
7611943
20.

Biphasic periodic paralysis.

Chesson AL Jr, Schochet SS Jr, Peters BH.

Arch Neurol. 1979 Nov;36(11):700-4.

PMID:
508128

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