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Items: 1 to 20 of 308

1.

Erythrokeratodermia variabilis with erythema gyratum repens-like lesions.

Landau M, Cohen-Bar-Dayan M, Hohl D, Ophir J, Wolf CR, Gat A, Mevorah B.

Pediatr Dermatol. 2002 Jul-Aug;19(4):285-92.

PMID:
12220269
2.

Erythrokeratodermia variabilis - variant with circumscribed variable erythema and periorificial fixed Bazex Dupré erythema.

Stănescu L, Georgescu CV, Georgescu AC, Georgescu I, Călin G.

Rom J Morphol Embryol. 2007;48(4):443-7.

3.

Erythrokeratodermia variabilis.

Maekawa Y, Yasaka S.

J Dermatol. 1977 Aug;4(4):147-50.

PMID:
15461342
4.

Progressive symmetrical erythrokeratoderma: report of a Turkish family and evaluation for loricrin and connexin gene mutations.

Akman A, Masse M, Mihci E, Richard G, Christiano AM, Balle BJ, Ciftcioglu MA, Alpsoy E.

Clin Exp Dermatol. 2008 Aug;33(5):582-4. doi: 10.1111/j.1365-2230.2008.02728.x. Epub 2008 May 7.

PMID:
18462442
5.

Progressive symmetric erythrokeratoderma: report of a Chinese family.

Yan HB, Zhang J, Liang W, Zhang HY, Liu JY.

Indian J Dermatol Venereol Leprol. 2011 Sep-Oct;77(5):597-600. doi: 10.4103/0378-6323.84070.

6.

The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron.

van Steensel MA, Oranje AP, van der Schroeff JG, Wagner A, van Geel M.

Am J Med Genet A. 2009 Feb 15;149A(4):657-61. doi: 10.1002/ajmg.a.32744.

PMID:
19291775
7.

Evidence for the absence of mutations at GJB3, GJB4 and LOR in progressive symmetrical erythrokeratodermia.

Wei S, Zhou Y, Zhang TD, Huang ZM, Zhang XB, Zhu HL, Liang BH, Lin L, Deng L.

Clin Exp Dermatol. 2011 Jun;36(4):399-405. doi: 10.1111/j.1365-2230.2010.03974.x. Epub 2010 Dec 24.

PMID:
21198793
8.

A case of erythrokeratoderma variabilis without mutations in connexin 31.

Ishida-Yamamoto A, Kelsell D, Common J, Houseman MJ, Hashimoto M, Shibaki H, Asano K, Takahashi H, Hashimoto Y, Senshu T, Leigh IM, Iizuka H.

Br J Dermatol. 2000 Dec;143(6):1283-7.

PMID:
11122035
9.

Loricrin keratoderma: a cause of congenital ichthyosiform erythroderma and collodion baby.

Matsumoto K, Muto M, Seki S, Saida T, Horiuchi N, Takahashi H, Ishida-Yamamoto A, Iizuka H.

Br J Dermatol. 2001 Oct;145(4):657-60.

PMID:
11703298
10.

Erythrokeratoderma variabilis-like ichthyosis in Chanarin-Dorfman syndrome.

Pujol RM, Gilaberte M, Toll A, Florensa L, Lloreta J, González-Enseñat MA, Fischer J, Azon A.

Br J Dermatol. 2005 Oct;153(4):838-41.

PMID:
16181472
11.

A new, recurrent mutation of GJB3 (Cx31) in erythrokeratodermia variabilis.

Morley SM, White MI, Rogers M, Wasserman D, Ratajczak P, McLean WH, Richard G.

Br J Dermatol. 2005 Jun;152(6):1143-8.

PMID:
15948974
12.

Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis.

Macari F, Landau M, Cousin P, Mevorah B, Brenner S, Panizzon R, Schorderet DF, Hohl D, Huber M.

Am J Hum Genet. 2000 Nov;67(5):1296-301. Epub 2000 Oct 3.

13.

[Bullous congenital ichthyosiform erythroderma of Brocq; 2 patients with different phenotype and genotype].

Lavrijsen AP, Bergman W, Steijlen PM.

Ned Tijdschr Geneeskd. 2001 Aug 4;145(31):1527-8. Dutch. No abstract available.

PMID:
11569466
14.

Unilateral hyperkeratotic plaques along blaschko lines.

Kumar P, Debbarman P, Rk S.

Dermatol Online J. 2015 Jul 15;21(7). pii: 13030/qt85w69792.

PMID:
26436980
15.

Hereditary palmoplantar (epidermolytic) keratoderma: illustration through a familial report.

Sehgal VN, Sardana K, Sharma S, Raut D.

Skinmed. 2004 Nov-Dec;3(6):323-30; quiz 331-2. Review.

PMID:
15538081
16.

[Family study of erythrokeratodermia figurata variabilis].

Itin P, Levy CA, Sommacal-Schopf D, Schnyder UW.

Hautarzt. 1992 Aug;43(8):500-4. German.

PMID:
1506216
17.

Erythrokeratoderma variabilis successfully treated with topical tazarotene.

Yoo S, Simzar S, Han K, Takahashi S, Cotliar R.

Pediatr Dermatol. 2006 Jul-Aug;23(4):382-5.

PMID:
16918639
18.

Annular epidermolytic ichthyosis: a unique phenotype.

Sahn EE, Weimer CE Jr, Garen PD.

J Am Acad Dermatol. 1992 Aug;27(2 Pt 2):348-55. Review.

PMID:
1517502
19.

Bullous congenital ichthyosiform erythroderma: a sporadic case produced by a new KRT10 gene mutation.

Betlloch I, Lucas Costa A, Mataix J, Pérez-Crespo M, Ballester I.

Pediatr Dermatol. 2009 Jul-Aug;26(4):489-91. doi: 10.1111/j.1525-1470.2009.00969.x.

PMID:
19689541
20.

Bullous congenital ichthyosiform erythroderma clinically resembling neonatal staphylococcal scalded skin syndrome.

Cheng S, Moss C, Upton CJ, Levell NJ.

Clin Exp Dermatol. 2009 Aug;34(6):747-8. doi: 10.1111/j.1365-2230.2008.03019.x. No abstract available.

PMID:
19635120
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