586 related articles for article (PubMed ID: 18360110)
1. 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. PubMed ID: 18360110
[TBL] [Abstract][Full Text] [Related]
2. 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; 16(5):507-10. PubMed ID: 17101470
[TBL] [Abstract][Full Text] [Related]
3. 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. PubMed ID: 15214894
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 15663507
[TBL] [Abstract][Full Text] [Related]
5. Nonsense mutations in KRT1 caused recessive epidermolytic palmoplantar keratoderma with knuckle pads.
Mo R; Lin M; Lee M; Yan W; Wang H; Lin Z
J Eur Acad Dermatol Venereol; 2022 Oct; 36(10):1857-1862. PubMed ID: 35490383
[TBL] [Abstract][Full Text] [Related]
6. A de novo mutation of KRT1 in a baby girl causing epidermolytic ichthyosis with impressive epidermolytic palmoplantar keratoderma.
Calì F; Failla P; Vinci M; Siragusa M; Schepis C
Dermatol Online J; 2020 Jul; 26(7):. PubMed ID: 32898404
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 20500210
[TBL] [Abstract][Full Text] [Related]
8. Analysis of the KRT9 gene in a Mexican family with epidermolytic palmoplantar keratoderma.
Lopez-Valdez J; Rivera-Vega MR; Gonzalez-Huerta LM; Cazarin J; Cuevas-Covarrubias S
Pediatr Dermatol; 2013; 30(3):354-8. PubMed ID: 23278372
[TBL] [Abstract][Full Text] [Related]
9. Mutation M157R of keratin 9 in a Chinese family with epidermolytic palmoplantar keratoderma.
Zhao JJ; Zhang ZH; Niu ZM; Xiang LH; Ye XY; Huang W; Zheng ZZ
Int J Dermatol; 2008 Jun; 47(6):634-7. PubMed ID: 18477167
[No Abstract] [Full Text] [Related]
10. Proteomic profiling reveals KRT6C as a probable hereterodimer partner for KRT9: New insights into re-classifying epidermolytic palmoplantar keratoderma (EPPK) and a milder form of pachyonychia congenita (PC-K6c) as a group of genetic cutaneous disorders.
Li P; Qi J; Zhong Y; Ding A; Xiao H
J Proteomics; 2023 Sep; 287():104971. PubMed ID: 37467889
[TBL] [Abstract][Full Text] [Related]
11. Epidermolytic hyperkeratosis.
Bale SJ; Compton JG; DiGiovanna JJ
Semin Dermatol; 1993 Sep; 12(3):202-9. PubMed ID: 7692917
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK).
Reis A; Hennies HC; Langbein L; Digweed M; Mischke D; Drechsler M; Schröck E; Royer-Pokora B; Franke WW; Sperling K
Nat Genet; 1994 Feb; 6(2):174-9. PubMed ID: 7512862
[TBL] [Abstract][Full Text] [Related]
15. Novel and recurrent mutations in keratin 1 cause epidermolytic ichthyosis and palmoplantar keratoderma.
Smith FJD; Kreuser-Genis IM; Jury CS; Wilson NJ; Terron-Kwiatowski A; Zamiri M
Clin Exp Dermatol; 2019 Jul; 44(5):528-534. PubMed ID: 30288772
[TBL] [Abstract][Full Text] [Related]
16. Annular epidermolytic ichthyosis with palmoplantar keratosis: a unique phenotype associated with interfamilial phenotypic heterogeneity.
Liang B; Yuan T; Zhou Y; Ding Y; Tang L; Wang F; Wang P; Li H; Zhang Y; Zhu M; Ji Y; Hong X; Zhang X; Zhu Q
Eur J Dermatol; 2020 Jun; 30(3):294-299. PubMed ID: 32666929
[TBL] [Abstract][Full Text] [Related]
17. A novel mutation of keratin 9 in a large Chinese family with epidermolytic palmoplantar keratoderma.
He XH; Zhang XN; Mao W; Chen HP; Xu LR; Chen H; He XL; Le YP
Br J Dermatol; 2004 Apr; 150(4):647-51. PubMed ID: 15099359
[TBL] [Abstract][Full Text] [Related]
18. A novel keratin 9 gene mutation (Asn160His) in a Taiwanese family with epidermolytic palmoplantar keratoderma.
Lin JH; Lin MH; Yang MH; Chao SC
Clin Exp Dermatol; 2004 May; 29(3):308-10. PubMed ID: 15115518
[TBL] [Abstract][Full Text] [Related]
19. Epidermolytic palmoplantar keratoderma of Vörner: re-evaluation of Vörner's original family and identification of a novel keratin 9 mutation.
Küster W; Reis A; Hennies HC
Arch Dermatol Res; 2002 Aug; 294(6):268-72. PubMed ID: 12192490
[TBL] [Abstract][Full Text] [Related]
20. 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. PubMed ID: 22250628
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
