Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 75

1.

Erythrokeratodermia variabilis: first Japanese case documenting GJB3 mutation.

Ikeya S, Urano S, Sakabe J, Ito T, Tokura Y.

J Dermatol. 2013 May;40(5):402-3. doi: 10.1111/1346-8138.12101. Epub 2013 Feb 27. No abstract available.

PMID:
23442023
2.

Mutation analysis of GJB3 and GJB4 in Chinese patients with erythrokeratodermia variabilis.

Liu H, Liu H, Fu XA, Yu YX, Zhou GZ, Lu XM, Tian HQ, Yu CP, Shi ZX, Yu ML, Zhang FR.

J Dermatol. 2012 Apr;39(4):400-1. doi: 10.1111/j.1346-8138.2011.01314.x. Epub 2011 Sep 28. No abstract available.

PMID:
21950330
3.

A missense mutation in the GJB3 gene responsible for erythrokeratodermia variabilis in a Chinese family.

Wang W, Liu LH, Chen G, Gao M, Zhu J, Zhou FS, Cheng H, Tang HY, Wu BY, Sun LD, Yang S, Wang PG, Zhang XJ.

Clin Exp Dermatol. 2012 Dec;37(8):919-21. doi: 10.1111/j.1365-2230.2012.04406.x. Epub 2012 Jun 8. No abstract available.

PMID:
22681493
4.

A novel GJB3 (Cx31) missense mutation in a Chinese patient with erythrokeratodermia variabilis.

Wang ZX, Lu WS, Li H, Lin D, Zhou FS, Sun LD, Yang S, Zhang XJ.

J Eur Acad Dermatol Venereol. 2011 Jan;25(1):113-5. doi: 10.1111/j.1468-3083.2010.03691.x. No abstract available.

PMID:
20497287
5.

An unusual missense mutation in the GJB3 gene resulting in severe erythrokeratodermia variabilis.

Glatz M, van Steensel MA, van Geel M, Steijlen PM, Wolf P.

Acta Derm Venereol. 2011 Oct;91(6):714-5. doi: 10.2340/00015555-1135. No abstract available.

6.

The novel GJB3 mutation p.Thr202Asn in the M4 transmembrane domain underlies erythrokeratodermia variabilis.

Sugiura K, Arima M, Matsunaga K, Akiyama M.

Br J Dermatol. 2015 Jul;173(1):309-11. doi: 10.1111/bjd.13641. Epub 2015 May 28. No abstract available.

PMID:
25556823
7.

Erythrokeratoderma variabilis caused by a recessive mutation in GJB3.

Fuchs-Telem D, Pessach Y, Mevorah B, Shirazi I, Sarig O, Sprecher E.

Clin Exp Dermatol. 2011 Jun;36(4):406-11. doi: 10.1111/j.1365-2230.2010.03986.x.

PMID:
21564177
8.

Erythrokeratodermia variabilis: report of two cases and a novel missense variant in GJB4 encoding connexin 30.3.

Kokotas H, Papagiannaki K, Grigoriadou M, Petersen MB, Katsarou A.

Eur J Dermatol. 2012 Mar-Apr;22(2):182-6. doi: 10.1684/ejd.2011.1617.

PMID:
22266302
9.

A sporadic elder case of erythrokeratodermia variabilis with a single base-pair transversion in GJB3 gene successfully treated with systemic vitamin A derivative.

Otaguchi R, Kawakami T, Matsuoka M, Kimura S, Soma Y, Matsuda M, Hamada T, Hashimoto T.

J Dermatol. 2014 Nov;41(11):1016-8. doi: 10.1111/1346-8138.12628. Epub 2014 Oct 9. No abstract available.

PMID:
25297803
10.

A case of erythrokeratodermia variabilis with connexin 31 gene mutation (Cx31F137L).

Torres T, Velho G, Sanches M, Selores M.

Int J Dermatol. 2012 Apr;51(4):494-6. doi: 10.1111/j.1365-4632.2010.04640.x. Epub 2011 Sep 14. No abstract available.

PMID:
21913904
11.

Familial erythrokeratodermia variabilis with pustular lesions: a new variant?

Zhang L, Huo W, Gao XH, Ma L, Xiu Y, Zheng S, Hong Y, Chen HD.

Acta Derm Venereol. 2010 May;90(3):274-8. doi: 10.2340/00015555-0821.

12.

Novel mutation in GJB4 gene (connexin 30.3) in a family with erythrokeratodermia variabilis.

Sbidian E, Bousseloua N, Jonard L, Leclerc-Mercier S, Bodemer C, Hadj-Rabia S.

Acta Derm Venereol. 2013 Mar 27;93(2):193-5. doi: 10.2340/00015555-1436. No abstract available.

13.

Novel and recurrent connexin 30.3 and connexin 31 mutations associated with erythrokeratoderma variabilis.

Scott CA, O'Toole EA, Mohungoo MJ, Messenger A, Kelsell DP.

Clin Exp Dermatol. 2011 Jan;36(1):88-90.

PMID:
21188847
14.

Case of erythrokeratodermia variabilis successfully treated with oral vitamin A.

Shizukawa H, Hiragun M, Hiragun T, Sugita Y, Hide M.

J Dermatol. 2015 Nov;42(11):1124-5. doi: 10.1111/1346-8138.13056. Epub 2015 Aug 18. No abstract available.

PMID:
26283448
15.

Erythrokeratodermia variabilis et progressiva.

Ishida-Yamamoto A.

J Dermatol. 2016 Mar;43(3):280-5. doi: 10.1111/1346-8138.13220. Review.

PMID:
26945536
16.

No exonic mutations at GJB2, GJB3, GJB4, GJB6, ARS (Component B), and LOR genes responsible for a Chinese patient affected by progressive symmetric erythrokeratodermia with pseudoainhum.

Zhou F, Fu H, Liu L, Cui Y, Zhang Z, Chang R, Yue Z, Yang S, Zhang X.

Int J Dermatol. 2014 Sep;53(9):1111-3. doi: 10.1111/ijd.12494. Epub 2014 Jun 25.

PMID:
24962725
17.

A new mutation in the GJB3 gene in a patient with erythrokeratodermia variabilis.

Renner R, Paasch U, Simon JC, Froster UG, Heinritz W.

J Eur Acad Dermatol Venereol. 2008 Jun;22(6):750-1. doi: 10.1111/j.1468-3083.2007.02447.x. No abstract available.

PMID:
18482034
18.

Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlations.

Richard G, Brown N, Rouan F, Van der Schroeff JG, Bijlsma E, Eichenfield LF, Sybert VP, Greer KE, Hogan P, Campanelli C, Compton JG, Bale SJ, DiGiovanna JJ, Uitto J.

J Invest Dermatol. 2003 Apr;120(4):601-9.

19.

Erythrokeratoderma Variabilis Caused by p.Gly45Glu in Connexin 31: Importance of the First Extracellular Loop Glycine Residue for Gap Junction Function.

Takeichi T, Sugiura K, Hsu CK, Nomura T, Takama H, Simpson MA, Shimizu H, McGrath JA, Akiyama M.

Acta Derm Venereol. 2016 May;96(4):557-9. doi: 10.2340/00015555-2307. Review. No abstract available.

20.

Erythrokeratodermia variabilis et progressiva allelic to oculo-dento-digital dysplasia.

Duchatelet S, Hovnanian A.

J Invest Dermatol. 2015 Jun;135(6):1475-8. doi: 10.1038/jid.2014.535.

Supplemental Content

Support Center