These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

198 related articles for article (PubMed ID: 17433175)

  • 1. 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]  

  • 2. 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]  

  • 3. Epidermolytic hyperkeratosis.
    Bale SJ; Compton JG; DiGiovanna JJ
    Semin Dermatol; 1993 Sep; 12(3):202-9. PubMed ID: 7692917
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Epidermolytic hyperkeratosis.
    Kwak J; Maverakis E
    Dermatol Online J; 2006 Sep; 12(5):6. PubMed ID: 16962021
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Clinical heterogeneity in epidermolytic hyperkeratosis.
    DiGiovanna JJ; Bale SJ
    Arch Dermatol; 1994 Aug; 130(8):1026-35. PubMed ID: 8053700
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Linear nevus comedonicus with epidermolytic hyperkeratosis.
    Schecter AK; Lester B; Pan TD; Robinson-Bostom L
    J Cutan Pathol; 2004 Aug; 31(7):502-5. PubMed ID: 15239681
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bullous congenital ichthyosiform erythroderma: a sporadic case produced by a new KRT10 gene mutation.
    Betlloch I; Lucas Costa A; Mataix J; Pérez-Crespo M; Ballester I
    Pediatr Dermatol; 2009; 26(4):489-91. PubMed ID: 19689541
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 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. 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]  

  • 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. Epidermolytic hyperkeratosis within infundibular cysts.
    Steele CL; Shea CR; Petronic-Rosic V
    J Cutan Pathol; 2007 Apr; 34(4):360-2. PubMed ID: 17381810
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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. PubMed ID: 10844506
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.