354 related articles for article (PubMed ID: 7692917)
1. Epidermolytic hyperkeratosis.
Bale SJ; Compton JG; DiGiovanna JJ
Semin Dermatol; 1993 Sep; 12(3):202-9. PubMed ID: 7692917
[TBL] [Abstract][Full Text] [Related]
2. Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q.
Compton JG; DiGiovanna JJ; Santucci SK; Kearns KS; Amos CI; Abangan DL; Korge BP; McBride OW; Steinert PM; Bale SJ
Nat Genet; 1992 Jul; 1(4):301-5. PubMed ID: 1284546
[TBL] [Abstract][Full Text] [Related]
3. 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; 15(7):1133-41. PubMed ID: 16505000
[TBL] [Abstract][Full Text] [Related]
4. Epidermolytic hyperkeratosis: applied molecular genetics.
DiGiovanna JJ; Bale SJ
J Invest Dermatol; 1994 Mar; 102(3):390-4. PubMed ID: 7509838
[TBL] [Abstract][Full Text] [Related]
5. Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens.
Rothnagel JA; Traupe H; Wojcik S; Huber M; Hohl D; Pittelkow MR; Saeki H; Ishibashi Y; Roop DR
Nat Genet; 1994 Aug; 7(4):485-90. PubMed ID: 7524919
[TBL] [Abstract][Full Text] [Related]
6. Epidermolytic hyperkeratosis type NPS-3: a case report.
Prohić A; Selmanagić A; Bilalović N
Acta Dermatovenerol Croat; 2007; 15(1):20-3. PubMed ID: 17433175
[TBL] [Abstract][Full Text] [Related]
7. Epidermolytic hyperkeratosis: a keratin 1 or 10 mutational event.
Lacz NL; Schwartz RA; Kihiczak G
Int J Dermatol; 2005 Jan; 44(1):1-6. PubMed ID: 15663649
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Epidermolytic hyperkeratosis.
Kwak J; Maverakis E
Dermatol Online J; 2006 Sep; 12(5):6. PubMed ID: 16962021
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma). Genetic linkage to chromosome 12q in the region of the type II keratin gene cluster.
Pulkkinen L; Christiano AM; Knowlton RG; Uitto J
J Clin Invest; 1993 Jan; 91(1):357-61. PubMed ID: 7678607
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A transgenic mouse model that recapitulates the clinical features of both neonatal and adult forms of the skin disease epidermolytic hyperkeratosis.
Bickenbach JR; Longley MA; Bundman DS; Dominey AM; Bowden PE; Rothnagel JA; Roop DR
Differentiation; 1996 Dec; 61(2):129-39. PubMed ID: 8983179
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. Systematized linear epidermolytic hyperkeratosis.
Kumar P; Kumar R; Mandal RK; Hassan S
Dermatol Online J; 2014 Jan; 20(1):21248. PubMed ID: 24456951
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis.
Arin MJ; Longley MA; Epstein EH; Rothnagel JA; Roop DR
Exp Dermatol; 2000 Feb; 9(1):16-9. PubMed ID: 10688370
[TBL] [Abstract][Full Text] [Related]
20. Genetic approaches to understanding the keratinopathies.
Bale SJ; DiGiovanna JJ
Adv Dermatol; 1997; 12():99-113; discussion 114. PubMed ID: 8973737
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]