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2. [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. PubMed ID: 21811984 [TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 20302579 [TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 17596149 [No Abstract] [Full Text] [Related]
5. 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. PubMed ID: 9184002 [TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 17973888 [TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 18219278 [TBL] [Abstract][Full Text] [Related]
8. Mild recessive epidermolytic hyperkeratosis associated with a novel keratin 10 donor splice-site mutation in a family of Norfolk terrier dogs. Credille KM; Barnhart KF; Minor JS; Dunstan RW Br J Dermatol; 2005 Jul; 153(1):51-8. PubMed ID: 16029326 [TBL] [Abstract][Full Text] [Related]
9. [Analysis of a neonate with bullous congenital ichthyosiform erythroderma with next generation sequencing]. Lyu Y; Shi C; Zhang K; Gao M; Liu Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Jun; 35(3):434-436. PubMed ID: 29896749 [TBL] [Abstract][Full Text] [Related]
10. Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis. Hotz A; Oji V; Bourrat E; Jonca N; Mazereeuw-Hautier J; Betz RC; Blume-Peytavi U; Stieler K; Morice-Picard F; Schönbuchner I; Markus S; Schlipf N; Fischer J Acta Derm Venereol; 2016 May; 96(4):473-8. PubMed ID: 26581228 [TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 22035476 [No Abstract] [Full Text] [Related]
13. 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. PubMed ID: 19200214 [No Abstract] [Full Text] [Related]
14. Use of the frozen section 'jelly-roll' technique to aid in the diagnosis of bullous congenital ichthyosiform erythroderma (epidermolytic hyperkeratosis). Galler B; Bowen C; Arnold J; Kobayashi T; Dalton SR J Cutan Pathol; 2016 May; 43(5):434-7. PubMed ID: 26969483 [TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 16361731 [TBL] [Abstract][Full Text] [Related]
16. 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; 19(4):333-6. PubMed ID: 19443303 [TBL] [Abstract][Full Text] [Related]
17. [Bullous congenital ichthyosiform erythroderma of Brocq; 2 patients with different phenotype and genotype]. Lavrijsen AP; Bergman W; Steijlen PM Ned Tijdschr Geneeskd; 2001 Aug; 145(31):1527-8. PubMed ID: 11569466 [No Abstract] [Full Text] [Related]
18. 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. PubMed ID: 17683385 [TBL] [Abstract][Full Text] [Related]
19. An atypical form of bullous congenital ichthyosiform erythroderma is caused by a mutation in the L12 linker region of keratin 1. Kremer H; Lavrijsen AP; McLean WH; Lane EB; Melchers D; Ruiter DJ; Mariman EC; Steijlen PM J Invest Dermatol; 1998 Dec; 111(6):1224-6. PubMed ID: 9856846 [TBL] [Abstract][Full Text] [Related]
20. 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. PubMed ID: 9856845 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]