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Results: 1 to 20 of 273

1.

Bullous ichthyosiform erythroderma in a child born to a parent with systematized linear epidermolytic hyperkeratosis.

Akhyani M, Kiavash K, Kamyab K.

Int J Dermatol. 2009 Feb;48(2):215-7. doi: 10.1111/j.1365-4632.2009.03569.x. No abstract available.

PMID:
19200214
[PubMed - indexed for MEDLINE]
2.

Epidermolytic hyperkeratosis: generalized form in children from parents with systematized linear form.

Nazzaro V, Ermacora E, Santucci B, Caputo R.

Br J Dermatol. 1990 Mar;122(3):417-22.

PMID:
2182100
[PubMed - indexed for MEDLINE]
3.

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

Betlloch I, Lucas Costa A, Mataix J, PĂ©rez-Crespo M, Ballester I.

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

PMID:
19689541
[PubMed - indexed for MEDLINE]
4.

New KRT10 gene mutation underlying the annular variant of bullous congenital ichthyosiform erythroderma with clinical worsening during pregnancy.

Sheth N, Greenblatt D, McGrath JA.

Br J Dermatol. 2007 Sep;157(3):602-4. Epub 2007 Jun 26. No abstract available.

PMID:
17596149
[PubMed - indexed for MEDLINE]
5.

Generalized epidermolytic hyperkeratosis in two unrelated children from parents with localized linear form, and prenatal diagnosis.

Chassaing N, Kanitakis J, Sportich S, Cordier-Alex MP, Titeux M, Calvas P, Claudy A, Berbis P, Hovnanian A.

J Invest Dermatol. 2006 Dec;126(12):2715-7. Epub 2006 Sep 21. No abstract available.

PMID:
16990804
[PubMed - indexed for MEDLINE]
Free Article
6.

Mild recessive bullous congenital ichthyosiform erythroderma due to a previously unidentified homozygous keratin 10 nonsense mutation.

Tsubota A, Akiyama M, Kanitakis J, Sakai K, Nomura T, Claudy A, Shimizu H.

J Invest Dermatol. 2008 Jul;128(7):1648-52. doi: 10.1038/sj.jid.5701257. Epub 2008 Jan 24.

PMID:
18219278
[PubMed - indexed for MEDLINE]
Free Article
7.

Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia.

Yamamoto M, Tsuda T, Otaki Y, Nakanishi T, Yamanishi K.

J Dermatol. 2012 Aug;39(8):716-8. doi: 10.1111/j.1346-8138.2011.01410.x. Epub 2011 Oct 31. No abstract available.

PMID:
22035476
[PubMed - indexed for MEDLINE]
8.

[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
[PubMed - indexed for MEDLINE]
9.

Generalized epidermolytic hyperkeratosis in a child born to a parent with systematized epidermolytic linear epidermal nevus.

Reddy BS, Thadeus J, Kumar SK, Jaishanker T, Garg BR.

Int J Dermatol. 1997 Mar;36(3):198-200. No abstract available.

PMID:
9159002
[PubMed - indexed for MEDLINE]
10.

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
[PubMed - indexed for MEDLINE]
11.

Bullous congenital ichthyosiform erythroderma of Brocq.

Kucharekova M, Mosterd K, Winnepenninckx V, van Geel M, Sommer A, van Steensel MA.

Int J Dermatol. 2007 Nov;46 Suppl 3:36-8.

PMID:
17973888
[PubMed - indexed for MEDLINE]
12.

A keratin 10 gene mutation (Arg156Cys) in a Japanese patient with bullous congenital ichthyosiform erythroderma.

Saeki H, Hattori N, Mitsui H, Adachi M, Imakado S, Ishibashi Y, Tamaki K.

J Dermatol. 2002 Mar;29(3):168-71.

PMID:
11990254
[PubMed - indexed for MEDLINE]
13.

A novel helix termination mutation in keratin 10 in annular epidermolytic ichthyosis, a variant of bullous congenital ichthyosiform erythroderma.

Suga Y, Duncan KO, Heald PW, Roop DR.

J Invest Dermatol. 1998 Dec;111(6):1220-3.

PMID:
9856845
[PubMed - indexed for MEDLINE]
14.

[Generalized skin change in a newborn infant: infectious, genetic or autoimmune cause? Epidermolytic ichthyosis].

Jaeger J, Andres C, Grosber M, Suarez IL, Zirbs M, Ring J, Brockow K.

MMW Fortschr Med. 2013 Mar 7;155(4):5, 72. German. No abstract available.

PMID:
23614180
[PubMed - indexed for MEDLINE]
15.

Phenotypic heterogeneity in bullous congenital ichthyosiform erythroderma: possible somatic mosaicism for keratin gene mutation in the mildly affected mother of the proband.

Nomura K, Umeki K, Hatayama I, Kuronuma T.

Arch Dermatol. 2001 Sep;137(9):1192-5.

PMID:
11559215
[PubMed - indexed for MEDLINE]
16.

[Case no. 7. Bullous dermatosis].

Fraitag S.

Ann Pathol. 2013 Jun;33(3):207-10. doi: 10.1016/j.annpat.2013.04.007. Epub 2013 May 30. Review. French. No abstract available.

PMID:
23790663
[PubMed - indexed for MEDLINE]
17.

A case of bullous congenital ichthyosiform erythroderma (BCIE) caused by a mutation in the 1A helix initiation motif of keratin 1.

Uezato H, Yamamoto Y, Kuwae C, Nonaka K, Oshiro M, Kariya K, Nonaka S.

J Dermatol. 2005 Oct;32(10):801-8.

PMID:
16361731
[PubMed - indexed for MEDLINE]
18.

[Mutation analysis of KRT10 gene in a patient with bullous congenital ichthyosiform erythroderma].

Zhang SD, Liu JJ, Tian W, Zhao ZJ, Zhao JJ.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):421-3. doi: 10.3760/cma.j.issn.1003-9406.2011.04.014. Chinese.

PMID:
21811984
[PubMed - indexed for MEDLINE]
19.

A novel mutation in the L12 domain of keratin 1 is associated with mild epidermolytic ichthyosis.

Bolling MC, Bladergroen RS, van Steensel MA, Willemsen M, Jonkman MF, van Geel M.

Br J Dermatol. 2010 Apr;162(4):875-9. doi: 10.1111/j.1365-2133.2009.09617.x.

PMID:
20500210
[PubMed - indexed for MEDLINE]
20.

A keratin K10 gene mutation in a Japanese patient with epidermolytic hyperkeratosis.

Nomura K, Meng X, Umeki K, Tamai K, Sawamura D, Hashimoto I, Kikuchi T.

Jpn J Hum Genet. 1997 Mar;42(1):217-23.

PMID:
9184002
[PubMed - indexed for MEDLINE]

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