Similar articles for PMID: 21094958

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1992	1
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2003	1
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1

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. Dabby R, et al. J Neurol Sci. 2011 Feb 15;301(1-2):90-2. doi: 10.1016/j.jns.2010.10.006. Epub 2010 Nov 20. J Neurol Sci. 2011. PMID: 21094958

2

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

Fischer TZ, Waxman SG. Fischer TZ, et al. Ann N Y Acad Sci. 2010 Jan;1184:196-207. doi: 10.1111/j.1749-6632.2009.05110.x. Ann N Y Acad Sci. 2010. PMID: 20146699 Review.

3

Painful channels.

Catterall WA, Yu FH. Catterall WA, et al. Neuron. 2006 Dec 7;52(5):743-4. doi: 10.1016/j.neuron.2006.11.017. Neuron. 2006. PMID: 17145494 Free article.

4

SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes.

Fertleman CR, Baker MD, Parker KA, Moffatt S, Elmslie FV, Abrahamsen B, Ostman J, Klugbauer N, Wood JN, Gardiner RM, Rees M. Fertleman CR, et al. Neuron. 2006 Dec 7;52(5):767-74. doi: 10.1016/j.neuron.2006.10.006. Neuron. 2006. PMID: 17145499 Free article.

5

Autosomal dominant erythermalgia associated with a novel mutation in the voltage-gated sodium channel alpha subunit Nav1.7.

Michiels JJ, te Morsche RH, Jansen JB, Drenth JP. Michiels JJ, et al. Arch Neurol. 2005 Oct;62(10):1587-90. doi: 10.1001/archneur.62.10.1587. Arch Neurol. 2005. PMID: 16216943

6

Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronism.

Edelheit O, Hanukoglu I, Gizewska M, Kandemir N, Tenenbaum-Rakover Y, Yurdakök M, Zajaczek S, Hanukoglu A. Edelheit O, et al. Clin Endocrinol (Oxf). 2005 May;62(5):547-53. doi: 10.1111/j.1365-2265.2005.02255.x. Clin Endocrinol (Oxf). 2005. PMID: 15853823 Review.

7

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. de Rooij AM, et al. Eur J Neurol. 2010 Jun 1;17(6):808-14. doi: 10.1111/j.1468-1331.2009.02931.x. Epub 2010 Jan 12. Eur J Neurol. 2010. PMID: 20074229

8

SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels.

Drenth JP, te Morsche RH, Guillet G, Taieb A, Kirby RL, Jansen JB. Drenth JP, et al. J Invest Dermatol. 2005 Jun;124(6):1333-8. doi: 10.1111/j.0022-202X.2005.23737.x. J Invest Dermatol. 2005. PMID: 15955112 Free article.

9

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. Goldberg YP, et al. Clin Genet. 2007 Apr;71(4):311-9. doi: 10.1111/j.1399-0004.2007.00790.x. Clin Genet. 2007. PMID: 17470132

10

Two novel mutations in SCN1A gene in Iranian patients with epilepsy.

Ebrahimi A, Houshmand M, Tonekaboni SH, Fallah Mahboob Passand MS, Zainali S, Moghadasi M. Ebrahimi A, et al. Arch Med Res. 2010 Apr;41(3):207-14. doi: 10.1016/j.arcmed.2010.04.007. Arch Med Res. 2010. PMID: 20682179

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