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Volumn 43, Issue 4, 2004, Pages 295-297

A newborn presenting with congenital blistering

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSINE; GENOMIC DNA; KERATIN; KERATOHYALIN; LEUCINE; PRIMER DNA; PROLINE; RETINOID DERIVATIVE; TAQ POLYMERASE; THYMINE;

EID: 2342439301     PISSN: 00119059     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-4632.2004.01907.x     Document Type: Review
Times cited : (5)

References (12)
  • 1
    • 0026574244 scopus 로고
    • Staphylococcal toxin-mediated syndromes in childhood
    • Resnick SD. Staphylococcal toxin-mediated syndromes in childhood. Semin Dermatol 1992; 11: 11-18.
    • (1992) Semin. Dermatol. , vol.11 , pp. 11-18
    • Resnick, S.D.1
  • 3
    • 0023011651 scopus 로고
    • Neonatal pemphigus vulgaris
    • Merlob P, Metzker A, Hazaz B, et al. Neonatal pemphigus vulgaris. Pediatrics 1986; 78: 1102-1105.
    • (1986) Pediatrics , vol.78 , pp. 1102-1105
    • Merlob, P.1    Metzker, A.2    Hazaz, B.3
  • 4
    • 0033537350 scopus 로고    scopus 로고
    • Primary persistent autoimmune disorder in a neonate
    • Bergman R, Sujov P, Peled M, et al. Primary persistent autoimmune disorder in a neonate. Lancet 1999; 353: 124.
    • (1999) Lancet , vol.353 , pp. 124
    • Bergman, R.1    Sujov, P.2    Peled, M.3
  • 5
    • 0032965997 scopus 로고    scopus 로고
    • Human keratin disease: The increasing spectrum of disease and subtlety of the phenotype-genotype correlation
    • Irvine AD, McLean WH. Human keratin disease: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation. Br J Dermatol 1999; 140: 815-828.
    • (1999) Br. J. Dermatol. , vol.140 , pp. 815-828
    • Irvine, A.D.1    McLean, W.H.2
  • 6
    • 0035169346 scopus 로고    scopus 로고
    • Molecular genetics of heritable blistering disorders
    • Uitto J, Pulkkinen L. Molecular genetics of heritable blistering disorders. Arch Dermatol 2001; 137: 1458-1461.
    • (2001) Arch. Dermatol. , vol.137 , pp. 1458-1461
    • Uitto, J.1    Pulkkinen, L.2
  • 7
    • 0028110879 scopus 로고
    • Clinical heterogeneity in epidermolytic hyperkeratosis
    • DiGiovanna JJ, Bale SJ. Clinical heterogeneity in epidermolytic hyperkeratosis. Arch Dermatol 1994; 130: 1026-1035.
    • (1994) Arch. Dermatol. , vol.130 , pp. 1026-1035
    • DiGiovanna, J.J.1    Bale, S.J.2
  • 9
    • 0026781694 scopus 로고
    • Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis
    • Rothnagel JA, Dominey AM, Dempsey LD, et al. Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis. Science 1992; 257: 1128-1130.
    • (1992) Science , vol.257 , pp. 1128-1130
    • Rothnagel, J.A.1    Dominey, A.M.2    Dempsey, L.D.3
  • 10
    • 0026699760 scopus 로고
    • The genetic basis of epidermolytic hyperkeratosis: A disorder of differentiation-specific epidermal keratin genes
    • Cheng J, Syder AJ, Yu QC, et al. The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes. Cell 1992; 70: 811-819.
    • (1992) Cell , vol.70 , pp. 811-819
    • Cheng, J.1    Syder, A.J.2    Yu, Q.C.3
  • 11
    • 0026612429 scopus 로고
    • A leucine-proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis
    • Chipev CC, Korge BP, Markova N, et al. A leucine-proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis. Cell 1992; 70: 821-828.
    • (1992) Cell , vol.70 , pp. 821-828
    • Chipev, C.C.1    Korge, B.P.2    Markova, N.3
  • 12
    • 0034872664 scopus 로고    scopus 로고
    • Phenotypic/genotypic correlations in patients with epidermolytic hyperkeratosis and the effects of retinoid therapy on keratin expression
    • Virtanen M, Gedde-Dahl T Jr, Mork NJ, et al. Phenotypic/genotypic correlations in patients with epidermolytic hyperkeratosis and the effects of retinoid therapy on keratin expression. Acta Derm Venereol 2001; 81: 163-170.
    • (2001) Acta. Derm. Venereol. , vol.81 , pp. 163-170
    • Virtanen, M.1    Gedde-Dahl Jr., T.2    Mork, N.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.