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 *

268 related articles for article (PubMed ID: 31190940)

  • 1. Epidermolytic hyperkeratosis: clinical update.
    Peter Rout D; Nair A; Gupta A; Kumar P
    Clin Cosmet Investig Dermatol; 2019; 12():333-344. PubMed ID: 31190940
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

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

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. A novel Y160C mutation of Keratin 10 gene in a Chinese male infant with epidermolytic hyperkeratosis.
    Zhao C; Li Y; Shi G; Shi X; Zhang G
    Turk J Pediatr; 2018; 60(4):426-428. PubMed ID: 30859768
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. A Novel non-sense Mutation in Keratin 10 Causes a Familial Case of Recessive Epidermolytic Ichthyosis.
    Gutierrez JA; Hannoush ZC; Vargas LG; Momany A; Garcia CC; Murray JC; Dunnwald M
    Mol Genet Genomic Med; 2013 Jul; 1(2):108-112. PubMed ID: 23957016
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Bullous diseases caused by
    Osipowicz K; Wertheim-Tysarowska K; Kwiek B; Jankowska E; Gos M; Charzewska A; Woźniak K; Kowalewski C
    Postepy Dermatol Alergol; 2021 Dec; 38(6):1032-1038. PubMed ID: 35126011
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Histopathologic characterization of epidermolytic hyperkeratosis: a systematic review of histology from the National Registry for Ichthyosis and Related Skin Disorders.
    Ross R; DiGiovanna JJ; Capaldi L; Argenyi Z; Fleckman P; Robinson-Bostom L
    J Am Acad Dermatol; 2008 Jul; 59(1):86-90. PubMed ID: 18571597
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Epidermal nevi and epidermolytic hyperkeratosis: A review of cases, highlighting indications for biopsy and genetics referral.
    Nelson JM; Isaac JM; Mervak JE; Mancuso JB; Chan MP; Arreola A; Cha KB
    Pediatr Dermatol; 2024 Jun; ():. PubMed ID: 38898621
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.