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Results: 1 to 20 of 171

1.

Two novel SCN9A mutations causing insensitivity to pain.

Nilsen KB, Nicholas AK, Woods CG, Mellgren SI, Nebuchennykh M, Aasly J.

Pain. 2009 May;143(1-2):155-8. doi: 10.1016/j.pain.2009.02.016. Epub 2009 Mar 21. Erratum in: Pain. 2009 Sep;145(1-2):264.

PMID:
19304393
[PubMed - indexed for MEDLINE]
2.

Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders.

Drenth JP, Waxman SG.

J Clin Invest. 2007 Dec;117(12):3603-9. Review.

PMID:
18060017
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations.

Goldberg YP, MacFarlane J, MacDonald ML, Thompson J, Dube MP, Mattice M, Fraser R, Young C, Hossain S, Pape T, Payne B, Radomski C, Donaldson G, Ives E, Cox J, Younghusband HB, Green R, Duff A, Boltshauser E, Grinspan GA, Dimon JH, Sibley BG, Andria G, Toscano E, Kerdraon J, Bowsher D, Pimstone SN, Samuels ME, Sherrington R, Hayden MR.

Clin Genet. 2007 Apr;71(4):311-9.

PMID:
17470132
[PubMed - indexed for MEDLINE]
4.

No mutations in the voltage-gated NaV1.7 sodium channel alpha1 subunit gene SCN9A in familial complex regional pain syndrome.

de Rooij AM, Gosso MF, Alsina-Sanchis E, Marinus J, van Hilten JJ, van den Maagdenberg AM.

Eur J Neurol. 2010 Jun 1;17(6):808-14. doi: 10.1111/j.1468-1331.2009.02931.x. Epub 2010 Jan 12.

PMID:
20074229
[PubMed - indexed for MEDLINE]
5.

A novel mutation in SCN9A in a child with congenital insensitivity to pain.

Shorer Z, Wajsbrot E, Liran TH, Levy J, Parvari R.

Pediatr Neurol. 2014 Jan;50(1):73-6. doi: 10.1016/j.pediatrneurol.2013.09.007. Epub 2013 Nov 1.

PMID:
24188911
[PubMed - indexed for MEDLINE]
6.

Two novel mutations of SCN9A (Nav1.7) are associated with partial congenital insensitivity to pain.

Staud R, Price DD, Janicke D, Andrade E, Hadjipanayis AG, Eaton WT, Kaplan L, Wallace MR.

Eur J Pain. 2011 Mar;15(3):223-30. doi: 10.1016/j.ejpain.2010.07.003. Epub 2010 Aug 7.

PMID:
20692858
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Primary erythermalgia as a sodium channelopathy: screening for SCN9A mutations: exclusion of a causal role of SCN10A and SCN11A.

Drenth JP, Te Morsche RH, Mansour S, Mortimer PS.

Arch Dermatol. 2008 Mar;144(3):320-4. doi: 10.1001/archderm.144.3.320.

PMID:
18347287
[PubMed - indexed for MEDLINE]
8.

An SCN9A channelopathy causes congenital inability to experience pain.

Cox JJ, Reimann F, Nicholas AK, Thornton G, Roberts E, Springell K, Karbani G, Jafri H, Mannan J, Raashid Y, Al-Gazali L, Hamamy H, Valente EM, Gorman S, Williams R, McHale DP, Wood JN, Gribble FM, Woods CG.

Nature. 2006 Dec 14;444(7121):894-8.

PMID:
17167479
[PubMed - indexed for MEDLINE]
9.

Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations.

Cox JJ, Sheynin J, Shorer Z, Reimann F, Nicholas AK, Zubovic L, Baralle M, Wraige E, Manor E, Levy J, Woods CG, Parvari R.

Hum Mutat. 2010 Sep;31(9):E1670-86. doi: 10.1002/humu.21325.

PMID:
20635406
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Two novel SCN9A gene heterozygous mutations may cause partial deletion of pain perception.

Yuan R, Zhang X, Deng Q, Si D, Wu Y, Gao F, Zhou B.

Pain Med. 2011 Oct;12(10):1510-4. doi: 10.1111/j.1526-4637.2011.01237.x. Epub 2011 Sep 21.

PMID:
21939494
[PubMed - indexed for MEDLINE]
11.

Pain perception is altered by a nucleotide polymorphism in SCN9A.

Reimann F, Cox JJ, Belfer I, Diatchenko L, Zaykin DV, McHale DP, Drenth JP, Dai F, Wheeler J, Sanders F, Wood L, Wu TX, Karppinen J, Nikolajsen L, Männikkö M, Max MB, Kiselycznyk C, Poddar M, Te Morsche RH, Smith S, Gibson D, Kelempisioti A, Maixner W, Gribble FM, Woods CG.

Proc Natl Acad Sci U S A. 2010 Mar 16;107(11):5148-53. doi: 10.1073/pnas.0913181107. Epub 2010 Mar 8.

PMID:
20212137
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Link between pain and olfaction in an inherited sodium channelopathy.

Zufall F, Pyrski M, Weiss J, Leinders-Zufall T.

Arch Neurol. 2012 Sep;69(9):1119-23. doi: 10.1001/archneurol.2012.21. Review.

PMID:
22733046
[PubMed - indexed for MEDLINE]
13.

Painful Na-channelopathies: an expanding universe.

Waxman SG.

Trends Mol Med. 2013 Jul;19(7):406-9. doi: 10.1016/j.molmed.2013.04.003. Epub 2013 May 8. Review.

PMID:
23664154
[PubMed - indexed for MEDLINE]
14.

A stop codon mutation in SCN9A causes lack of pain sensation.

Ahmad S, Dahllund L, Eriksson AB, Hellgren D, Karlsson U, Lund PE, Meijer IA, Meury L, Mills T, Moody A, Morinville A, Morten J, O'donnell D, Raynoschek C, Salter H, Rouleau GA, Krupp JJ.

Hum Mol Genet. 2007 Sep 1;16(17):2114-21. Epub 2007 Jun 27.

PMID:
17597096
[PubMed - indexed for MEDLINE]
Free Article
15.

Paroxysmal extreme pain disorder M1627K mutation in human Nav1.7 renders DRG neurons hyperexcitable.

Dib-Hajj SD, Estacion M, Jarecki BW, Tyrrell L, Fischer TZ, Lawden M, Cummins TR, Waxman SG.

Mol Pain. 2008 Sep 19;4:37. doi: 10.1186/1744-8069-4-37.

PMID:
18803825
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

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
[PubMed - indexed for MEDLINE]
17.

Chronic non-paroxysmal neuropathic pain - Novel phenotype of mutation in the sodium channel SCN9A gene.

Dabby R, Sadeh M, Gilad R, Lampl Y, Cohen S, Inbar S, Leshinsky-Silver E.

J Neurol Sci. 2011 Feb 15;301(1-2):90-2. doi: 10.1016/j.jns.2010.10.006. Epub 2010 Nov 20.

PMID:
21094958
[PubMed - indexed for MEDLINE]
18.

Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia.

Yang Y, Wang Y, Li S, Xu Z, Li H, Ma L, Fan J, Bu D, Liu B, Fan Z, Wu G, Jin J, Ding B, Zhu X, Shen Y.

J Med Genet. 2004 Mar;41(3):171-4.

PMID:
14985375
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Sodium channelopathies and pain.

Lampert A, O'Reilly AO, Reeh P, Leffler A.

Pflugers Arch. 2010 Jul;460(2):249-63. doi: 10.1007/s00424-009-0779-3. Epub 2010 Jan 26. Review.

PMID:
20101409
[PubMed - indexed for MEDLINE]
20.

A SCN9A gene-encoded dorsal root ganglia sodium channel polymorphism associated with severe fibromyalgia.

Vargas-Alarcon G, Alvarez-Leon E, Fragoso JM, Vargas A, Martinez A, Vallejo M, Martinez-Lavin M.

BMC Musculoskelet Disord. 2012 Feb 20;13:23. doi: 10.1186/1471-2474-13-23.

PMID:
22348792
[PubMed - indexed for MEDLINE]
Free PMC Article

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