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 *

270 related articles for article (PubMed ID: 3522665)

  • 1. Ichthyosis bullosa of Siemens: a unique type of epidermolytic hyperkeratosis.
    Traupe H; Kolde G; Hamm H; Happle R
    J Am Acad Dermatol; 1986 Jun; 14(6):1000-5. PubMed ID: 3522665
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ichthyosis bullosa of Siemens: further delineation of the phenotype.
    Steijlen PM; Perret CM; Schuurmans Stekhoven JH; Ruiter DJ; Happle R
    Arch Dermatol Res; 1990; 282(1):1-5. PubMed ID: 2138447
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ichthyosis bullosa of Siemens: response to topical tazarotene.
    Rajiv S; Rakhesh SV
    Indian J Dermatol Venereol Leprol; 2006; 72(1):43-6. PubMed ID: 16481710
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A novel mutation in the 2B domain of keratin 2e causing ichthyosis bullosa of Siemens.
    Irvine AD; Smith FJ; Shum KW; Williams HC; McLean WH
    Clin Exp Dermatol; 2000 Nov; 25(8):648-51. PubMed ID: 11167982
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ichthyosis bullosa of Siemens is caused by mutations in the keratin 2e gene.
    Kremer H; Zeeuwen P; McLean WH; Mariman EC; Lane EB; van de Kerkhof CM; Ropers HH; Steijlen PM
    J Invest Dermatol; 1994 Sep; 103(3):286-9. PubMed ID: 8077693
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel asparagine-->aspartic acid mutation in the rod 1A domain in keratin 2e in a Japanese family with ichthyosis bullosa of Siemens.
    Takizawa Y; Akiyama M; Nagashima M; Shimizu H
    J Invest Dermatol; 2000 Jan; 114(1):193-5. PubMed ID: 10620137
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ichthyosis bullosa of Siemens and bullous ichthyosiform erythroderma--variants of the same disease?
    Murdoch ME; Leigh IM
    Clin Exp Dermatol; 1990 Jan; 15(1):53-6. PubMed ID: 2178822
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of Siemens.
    Arin MJ; Longley MA; Epstein EH; Scott G; Goldsmith LA; Rothnagel JA; Roop DR
    J Invest Dermatol; 1999 Mar; 112(3):380-2. PubMed ID: 10084318
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Bullous ichthyosis. A particular form of epidermolytic hyperkeratosis].
    Mariano MA; Ferreira L; Baptista AP; Blanchet-Bardon C
    Med Cutan Ibero Lat Am; 1989; 17(6):379-82. PubMed ID: 2699637
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ichthyosis bullosa of Siemens: its correct diagnosis facilitated by molecular genetic testing.
    Akiyama M; Tsuji-Abe Y; Yanagihara M; Nakajima K; Kodama H; Yaosaka M; Abe M; Sawamura D; Shimizu H
    Br J Dermatol; 2005 Jun; 152(6):1353-6. PubMed ID: 15949009
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epidermolytic hyperkeratosis: generalized form in children from parents with systematized linear form.
    Nazzaro V; Ermacora E; Santucci B; Caputo R
    Br J Dermatol; 1990 Mar; 122(3):417-22. PubMed ID: 2182100
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literature.
    Basarab T; Smith FJ; Jolliffe VM; McLean WH; Neill S; Rustin MH; Eady RA
    Br J Dermatol; 1999 Apr; 140(4):689-95. PubMed ID: 10233323
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ichthyosis bullosa of Siemens--a disease involving keratin 2e.
    McLean WH; Morley SM; Lane EB; Eady RA; Griffiths WA; Paige DG; Harper JI; Higgins C; Leigh IM
    J Invest Dermatol; 1994 Sep; 103(3):277-81. PubMed ID: 7521371
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic linkage of the keratin type II gene cluster with ichthyosis bullosa of Siemens and with autosomal dominant ichthyosis exfoliativa.
    Steijlen PM; Kremer H; Vakilzadeh F; Happle R; Lavrijsen AP; Ropers HH; Mariman EC
    J Invest Dermatol; 1994 Sep; 103(3):282-5. PubMed ID: 7521372
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Annular epidermolytic ichthyosis: a unique phenotype.
    Sahn EE; Weimer CE; Garen PD
    J Am Acad Dermatol; 1992 Aug; 27(2 Pt 2):348-55. PubMed ID: 1517502
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new variant of autosomal recessive exfoliative ichthyosis.
    Zvulunov A; Cagnano E; Kachko L; Shorer Z; Elbedour K; Stevens H
    Pediatr Dermatol; 2002; 19(5):382-7. PubMed ID: 12383092
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A glutamate to lysine mutation at the end of 2B rod domain of keratin 2e gene in ichthyosis bullosa of Siemens.
    Yang JM; Lee ES; Kang HJ; Choi GS; Yoneda K; Jung SY; Park KB; Steinert PM; Lee ES
    Acta Derm Venereol; 1998 Nov; 78(6):417-9. PubMed ID: 9833038
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Genetic skin diseases.
    Francis JS
    Curr Opin Pediatr; 1994 Aug; 6(4):447-53. PubMed ID: 7951667
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.