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Items: 10

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1.

Sporadic onset of erythermalgia: a gain-of-function mutation in Nav1.7.

Han C, Rush AM, Dib-Hajj SD, Li S, Xu Z, Wang Y, Tyrrell L, Wang X, Yang Y, Waxman SG.

Ann Neurol. 2006 Mar;59(3):553-8.

PMID:
16392115
2.

Erythermalgia: molecular basis for an inherited pain syndrome.

Waxman SG, Dib-Hajj S.

Trends Mol Med. 2005 Dec;11(12):555-62. Epub 2005 Nov 8. Review.

PMID:
16278094
3.

[From gene to disease; primary erythermalgia--a neuropathic disease as a consequence of mutations in a sodium pump gene].

Drenth JP, te Morsche RH, Michiels JJ.

Ned Tijdschr Geneeskd. 2006 Jan 28;150(4):194-6. Review. Dutch.

PMID:
16471234
4.

Familial pain syndromes from mutations of the NaV1.7 sodium channel.

Fischer TZ, Waxman SG.

Ann N Y Acad Sci. 2010 Jan;1184:196-207. doi: 10.1111/j.1749-6632.2009.05110.x. Review.

PMID:
20146699
5.

Genetics and molecular pathophysiology of Na(v)1.7-related pain syndromes.

Dib-Hajj SD, Yang Y, Waxman SG.

Adv Genet. 2008;63:85-110. doi: 10.1016/S0065-2660(08)01004-3. Review.

PMID:
19185186
6.

Severe case and literature review of primary erythromelalgia: novel SCN9A gene mutation.

Skeik N, Rooke TW, Davis MD, Davis DM, Kalsi H, Kurth I, Richardson RC.

Vasc Med. 2012 Feb;17(1):44-9. doi: 10.1177/1358863X11422584. Epub 2011 Oct 27. Review.

PMID:
22033523
7.

Pain disorders and erythromelalgia caused by voltage-gated sodium channel mutations.

Dabby R.

Curr Neurol Neurosci Rep. 2012 Feb;12(1):76-83. doi: 10.1007/s11910-011-0233-8. Review.

PMID:
21984269
8.

Voltage-dependent Na(v)1.7 sodium channels: multiple roles in adrenal chromaffin cells and peripheral nervous system.

Wada A, Wanke E, Gullo F, Schiavon E.

Acta Physiol (Oxf). 2008 Feb;192(2):221-31. Epub 2007 Nov 16. Review.

PMID:
18021327
9.

An atypical case of SCN9A mutation presenting with global motor delay and a severe pain disorder.

Meijer IA, Vanasse M, Nizard S, Robitaille Y, Rossignol E.

Muscle Nerve. 2014 Jan;49(1):134-8. doi: 10.1002/mus.23968. Epub 2013 Nov 22. Review.

PMID:
23893323
10.

[Erythermalgia, rare acrosyndrome. 13 cases].

Lazareth I, Fiessinger JN, Priollet P.

Presse Med. 1988 Nov 26;17(42):2235-9. Review. French.

PMID:
2974588

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