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Results: 1 to 20 of 706

Similar articles for PubMed (Select 19443303)

1.

Epidermolytic hyperkeratosis with palmoplantar keratoderma in a patient with KRT10 mutation.

Morais P, Mota A, Baudrier T, Lopes JM, Cerqueira R, Tavares P, Azevedo F.

Eur J Dermatol. 2009 Jul-Aug;19(4):333-6. doi: 10.1684/ejd.2009.0684. Epub 2009 May 14.

PMID:
19443303
2.
3.

Phenotypic/genotypic correlations in patients with epidermolytic hyperkeratosis and the effects of retinoid therapy on keratin expression.

Virtanen M, Gedde-Dahl T Jr, Mörk NJ, Leigh I, Bowden PE, Vahlquist A.

Acta Derm Venereol. 2001 Jun-Jul;81(3):163-70.

PMID:
11558869
4.

Epidermolytic hyperkeratosis type PS-1 caused by aberrant splicing of KRT1.

Tal O, Bergman R, Alcalay J, Indelman M, Sprecher E.

Clin Exp Dermatol. 2005 Jan;30(1):64-7.

PMID:
15663507
5.

Epidcermolytic hyperkeratosis: a case report.

Achar A, Naskar B, Laha R, Ray S.

J Indian Med Assoc. 2009 Mar;107(3):171-2.

PMID:
19810387
6.

Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice-site mutation in KRT10.

Covaciu C, Castori M, De Luca N, Ghirri P, Nannipieri A, Ragone G, Zambruno G, Castiglia D.

Br J Dermatol. 2010 Jun;162(6):1384-7. doi: 10.1111/j.1365-2133.2010.09665.x. Epub 2010 Mar 10.

PMID:
20302579
7.

Epidermolytic hyperkeratosis.

Kwak J, Maverakis E.

Dermatol Online J. 2006 Sep 8;12(5):6.

PMID:
16962021
8.

A recurrent missense mutation of keratin 1 gene in a Chinese family with epidermolytic hyperkeratosis (severe palmoplantar hyperkeratosis, type 1).

Zeng YP, Chai WX, Fang K, Sun QN, Zuo YG.

Int J Dermatol. 2012 Feb;51(2):182-5. doi: 10.1111/j.1365-4632.2011.05202.x.

PMID:
22250628
9.

Identification of a de novo keratin 1 mutation in epidermolytic hyperkeratosis with palmoplantar involvement.

Math A, Frank J, Handisurya A, Poblete-Gutiérrez P, Slupetzky K, Födinger D, Winter D, Stingl G, Kirnbauer R.

Eur J Dermatol. 2006 Sep-Oct;16(5):507-10.

PMID:
17101470
10.

Epidermolytic hyperkeratosis with polycyclic psoriasiform plaques resulting from a mutation in the keratin 1 gene.

Michael EJ, Schneiderman P, Grossman ME, Christiano AM.

Exp Dermatol. 1999 Dec;8(6):501-3.

PMID:
10597140
11.

Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene.

Terron-Kwiatkowski A, Terrinoni A, Didona B, Melino G, Atherton DJ, Irvine AD, McLean WH.

Br J Dermatol. 2004 Jun;150(6):1096-103.

PMID:
15214894
12.

A unique pattern of dyskeratosis characterizes epidermolytic hyperkeratosis and epidermolytic palmoplantar keratoderma.

Bergman R, Khamaysi Z, Sprecher E.

Am J Dermatopathol. 2008 Apr;30(2):101-5. doi: 10.1097/DAD.0b013e3181614898.

PMID:
18360110
13.

Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis.

Arin MJ, Oji V, Emmert S, Hausser I, Traupe H, Krieg T, Grimberg G.

Br J Dermatol. 2011 Feb;164(2):442-7. doi: 10.1111/j.1365-2133.2010.10096.x.

PMID:
21271994
14.

Keratin 1 and keratin 10 mutations causing epidermolytic hyperkeratosis in Chinese patients.

Sun XK, Ma LL, Xie YQ, Zhu XJ.

J Dermatol Sci. 2002 Sep;29(3):195-200.

PMID:
12234709
15.

R156C mutation of keratin 10 causes mild form of epidermolytic hyperkeratosis.

Haruna K, Suga Y, Mizuno Y, Hasegawa T, Kourou K, Matsuba S, Muramatsu S, Ikeda S.

J Dermatol. 2007 Aug;34(8):545-8.

PMID:
17683385
16.

Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratoderma.

Navsaria HA, Swensson O, Ratnavel RC, Shamsher M, McLean WH, Lane EB, Griffiths D, Eady RA, Leigh IM.

J Invest Dermatol. 1995 Mar;104(3):425-9.

PMID:
7532198
17.

Epidermolytic hyperkeratosis in a Hispanic family resulting from a mutation in the keratin 1 gene.

Cserhalmi-Friedman PB, Squeo R, Gordon D, Garzon M, Schneiderman P, Grossman ME, Christiano AM.

Clin Exp Dermatol. 2000 May;25(3):241-3.

PMID:
10844506
18.

A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis.

Müller FB, Huber M, Kinaciyan T, Hausser I, Schaffrath C, Krieg T, Hohl D, Korge BP, Arin MJ.

Hum Mol Genet. 2006 Apr 1;15(7):1133-41. Epub 2006 Feb 27.

19.

Epidermolytic hyperkeratosis: a keratin 1 or 10 mutational event.

Lacz NL, Schwartz RA, Kihiczak G.

Int J Dermatol. 2005 Jan;44(1):1-6. Review.

PMID:
15663649
20.

Epidermolytic hyperkeratosis type NPS-3: a case report.

Prohić A, Selmanagić A, Bilalović N.

Acta Dermatovenerol Croat. 2007;15(1):20-3.

PMID:
17433175
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