Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 106

1.

Autosomal dominant erythromelalgia.

Finley WH, Lindsey JR Jr, Fine JD, Dixon GA, Burbank MK.

Am J Med Genet. 1992 Feb 1;42(3):310-5.

PMID:
1536168
2.

Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia.

Burns TM, Te Morsche RH, Jansen JB, Drenth JP.

Br J Dermatol. 2005 Jul;153(1):174-7.

PMID:
16029345
3.

Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons.

Dib-Hajj SD, Rush AM, Cummins TR, Hisama FM, Novella S, Tyrrell L, Marshall L, Waxman SG.

Brain. 2005 Aug;128(Pt 8):1847-54. Epub 2005 Jun 15.

PMID:
15958509
4.

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.

Arch Neurol. 2005 Oct;62(10):1587-90.

PMID:
16216943
5.

Hereditary erythermalgia and acquired erythromelalgia.

van Genderen PJ, Michiels JJ, Drenth JP.

Am J Med Genet. 1993 Feb 15;45(4):530-2. No abstract available.

PMID:
8465864
6.
7.

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.

8.

Erythromelalgia.

Thompson GH, Hahn G, Rang M.

Clin Orthop Relat Res. 1979 Oct;(144):249-54.

PMID:
535232
9.

Treatment with carbamazepine and gabapentin of a patient with primary erythermalgia (erythromelalgia) identified to have a mutation in the SCN9A gene, encoding a voltage-gated sodium channel.

Natkunarajah J, Atherton D, Elmslie F, Mansour S, Mortimer P.

Clin Exp Dermatol. 2009 Dec;34(8):e640-2. doi: 10.1111/j.1365-2230.2009.03355.x. Epub 2009 Jun 22.

PMID:
19549232
10.

Erythromelalgia: a hereditary pain syndrome enters the molecular era.

Waxman SG, Dib-Hajj SD.

Ann Neurol. 2005 Jun;57(6):785-8.

PMID:
15929046
11.

[Familial erythermalgia treated with pizotifen].

Guillet MH, Le Noach E, Milochau P, Sassolas B, Guillet G.

Ann Dermatol Venereol. 1995;122(11-12):777-9. Review. French.

PMID:
8729824
12.

Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family.

Sobrido MJ, Fernández JM, Fontoira E, Pérez-Sousa C, Cabello A, Castro M, Teijeira S, Alvarez S, Mederer S, Rivas E, Seijo-Martínez M, Navarro C.

Brain. 2005 Jul;128(Pt 7):1716-27. Epub 2005 Apr 27.

PMID:
15857933
13.

[On the clinical features of erythromelalgia. Familial incidence of an idiopathic form in mother and daughter].

Krebs A, Andres HU.

Schweiz Med Wochenschr. 1969 Mar 15;99(11):344-9. German. No abstract available.

PMID:
5795636
14.

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
15.

Compound heterozygosity in sodium channel Nav1.7 in a family with hereditary erythermalgia.

Samuels ME, te Morsche RH, Lynch ME, Drenth JP.

Mol Pain. 2008 Jun 2;4:21. doi: 10.1186/1744-8069-4-21.

16.

The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32.

Drenth JP, Finley WH, Breedveld GJ, Testers L, Michiels JJ, Guillet G, Taieb A, Kirby RL, Heutink P.

Am J Hum Genet. 2001 May;68(5):1277-82. Epub 2001 Mar 20.

17.

A family with whistling-face-syndrome.

Wettstein A, Buchinger G, Braun A, von Bazan UB.

Hum Genet. 1980;55(2):177-89.

PMID:
7450762
18.

A family with autosomal dominant hypocalcaemia with hypercalciuria (ADHH): mutational analysis, phenotypic variability and treatment challenges.

Burren CP, Curley A, Christie P, Rodda CP, Thakker RV.

J Pediatr Endocrinol Metab. 2005 Jul;18(7):689-99.

PMID:
16128246
19.

Skin perfusion in patients with erythromelalgia.

Littleford RC, Khan F, Belch JJ.

Eur J Clin Invest. 1999 Jul;29(7):588-93.

PMID:
10411664
20.

Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?

Ma S, Davis TL, Blair MA, Fang JY, Bradford Y, Haines JL, Hedera P.

Mov Disord. 2006 Sep;21(9):1368-74.

PMID:
16721753

Supplemental Content

Support Center