메뉴 건너뛰기




Volumn 6, Issue 3, 2012, Pages 78-81

Ichthyosis bullosa of siemens

Author keywords

Epidermolytic hyperkeratosis; Ichthyosis bullosa of siemens

Indexed keywords

CELESTAMINE; EMOLLIENT AGENT; PETROLATUM;

EID: 84872933586     PISSN: None     EISSN: 18987249     Source Type: Journal    
DOI: 10.3315/jdcr.2012.1107     Document Type: Article
Times cited : (6)

References (10)
  • 1
    • 13444279113 scopus 로고    scopus 로고
    • Epidermolytic hy-perkeratosis: A keratin 1 or 10 mutational event
    • Lacz NL, Schwartz RA, Kihiczak G. Epidermolytic hy-perkeratosis: a keratin 1 or 10 mutational event. Int J Dermatol. 2005; 44: 1-6.
    • (2005) Int J Dermatol , vol.44 , pp. 1-6
    • Lacz, N.L.1    Schwartz, R.A.2    Kihiczak, G.3
  • 2
    • 33645083734 scopus 로고    scopus 로고
    • A sporadic case of epidermolytic hyperkeratosis caused by a novel point mutation in the keratin 1 ge-ne
    • Shimomura Y, Sato N, Tomiyama K, Takahashi A, Ito M. A sporadic case of epidermolytic hyperkeratosis caused by a novel point mutation in the keratin 1 ge-ne. Clin Exp Dermatol. 2006; 31: 286-287.
    • (2006) Clin Exp Dermatol , vol.31 , pp. 286-287
    • Shimomura, Y.1    Sato, N.2    Tomiyama, K.3    Takahashi, A.4    Ito, M.5
  • 3
    • 0032932761 scopus 로고    scopus 로고
    • Ichthyosis bullosa of Siemens: Report of a family with evidence of a keratin 2e muta-tion, and a review of the literature
    • Basarab T, Smith FJ, Jolliffe VM, McLean WH, Neill S, Rustin MH, Eady RA. Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e muta-tion, and a review of the literature. Br J Dermatol. 1999; 140: 689-695.
    • (1999) Br J Dermatol , vol.140 , pp. 689-695
    • Basarab, T.1    Smith, F.J.2    Jolliffe, V.M.3    McLean, W.H.4    Neill, S.5    Rustin, M.H.6    Eady, R.A.7
  • 4
    • 0038326541 scopus 로고    scopus 로고
    • The molecular genetics of keratin disorders
    • Smith F. The molecular genetics of keratin disorders. Am J Clin Dermatol. 2003; 4: 347-364.
    • (2003) Am J Clin Dermatol , vol.4 , pp. 347-364
    • Smith, F.1
  • 6
    • 0033361793 scopus 로고    scopus 로고
    • 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. Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1. Am J Hum Genet. 1999; 64: 732-738.
    • (1999) Am J Hum Genet , vol.64 , pp. 732-738
    • Sybert, V.P.1    Francis, J.S.2    Corden, L.D.3    Smith, L.T.4    Weaver, M.5    Stephens, K.6    McLean, W.H.7
  • 8
    • 0034793372 scopus 로고    scopus 로고
    • New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ich-thyosis bullosa of Siemens
    • Whittock NV, Ashton GH, Griffiths WA, Eady RA, McGrath JA. New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ich-thyosis bullosa of Siemens. Br J Dermatol. 2001; 145: 330-335.
    • (2001) Br J Dermatol , vol.145 , pp. 330-335
    • Whittock, N.V.1    Ashton, G.H.2    Griffiths, W.A.3    Eady, R.A.4    McGrath, J.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.