BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

382 related articles for article (PubMed ID: 16962021)

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

  • 2. Epidcermolytic hyperkeratosis: a case report.
    Achar A; Naskar B; Laha R; Ray S
    J Indian Med Assoc; 2009 Mar; 107(3):171-2. PubMed ID: 19810387
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Epidermolytic hyperkeratosis.
    Bale SJ; Compton JG; DiGiovanna JJ
    Semin Dermatol; 1993 Sep; 12(3):202-9. PubMed ID: 7692917
    [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. Unilateral hyperkeratotic plaques along blaschko lines.
    Kumar P; Debbarman P; Rk S
    Dermatol Online J; 2015 Jul; 21(7):. PubMed ID: 26436980
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 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 novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythroderma.
    Joh GY; Traupe H; Metze D; Nashan D; Huber M; Hohl D; Longley MA; Rothnagel JA; Roop DR
    J Invest Dermatol; 1997 Mar; 108(3):357-61. PubMed ID: 9036939
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. 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]  

  • 17. Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1.
    Sybert VP; Francis JS; Corden LD; Smith LT; Weaver M; Stephens K; McLean WH
    Am J Hum Genet; 1999 Mar; 64(3):732-8. PubMed ID: 10053007
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Linkage of the epidermolytic hyperkeratosis phenotype and the region of the type II keratin gene cluster on chromosome 12.
    Bonifas JM; Bare JW; Chen MA; Lee MK; Slater CA; Goldsmith LA; Epstein EH
    J Invest Dermatol; 1992 Nov; 99(5):524-7. PubMed ID: 1385543
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis.
    Rothnagel JA; Lin MT; Longley MA; Holder RA; Hazen PG; Levy ML; Roop DR
    Prenat Diagn; 1998 Aug; 18(8):826-30. PubMed ID: 9742571
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 20.