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白色丘疹样营养不良型大疱性表皮松解症1例 被引量:2

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作者 杨鲲鹏
出处 《岭南皮肤性病科杂志》 2008年第3期176-177,共2页 Southern China Journal of Dermato-Venereology
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参考文献3

  • 1Odom RB,James WD, Berge TG. AndrewsDiseases of the Skin - Clinical Dermatology [ M ]. 9th Edition, Science Press ,2001:696.
  • 2Kou A, Nomura K, Pulkkinen L, et al. Novel glycine substitution mutations in COLTA1 reveal that the pasini and cock - ayne - touraine variants of dominant dystrophia epidermolysis bullosa are allekic [ J ]. J Invest Dermatol. 1997, 109:684 -687.
  • 3吴艳,朱学骏.先天性大疱性表皮松解症基底膜带分子的研究[J].中国麻风皮肤病杂志,2001,17(1):1-4. 被引量:4

二级参考文献10

  • 1[1]Fine JD, Bauer EA, Briggaman RA, et al. Revised clinical andlaboratory creteria for subtype of inherited epidermolysis bullosa. JAm Acad Dermatol, 1991,24:119
  • 2[2]Diaz LA, Giudice GJ. End of the century overview of skin blisters.Arch Dermatol, 2000,136:106
  • 3[3]Hashimoto I, Schnyder UW, Anton-Lamprecht I, et al. Epidermol-ysis bullosa herditaria with junctional blistering in an adult. Derma-tologica, 1976,125:72
  • 4[4]Hinter H, Wolff K. Generralized atrophic benign epidermolysis bul-losa. Arch Dermatol, 1982,118: 375
  • 5[5]McGrath JA, Pulkkinen L, Christiano AM, et al. Altered laminin 5expression due to mutations in the gene encoding the β 3 chain(LAMB3) in generalized atrophic benign epidermolysis bullosa. JInvest Dermatol, 1995,104: 467
  • 6[6]Darling TN, McGrath JA, Yee C, et al. Premature termination co-dens are present on both alleles of the bullous pemphigoid antigen 2/type XⅧ collagen gene in five Austrian families with generalizedepidermalysis bullosa. J Invest Dermatol, 1997,108(4) :463
  • 7[7]Floeth M, Fiedorowicz J, Shacke H, et al. Novel homozygous and-compound heterozygous COL17A1 mutation associated with junctionalepidermolysis bullosa. Invest Dermatol, 1998,111:528
  • 8[8]McGrath JA, Darling TN, Gatalica B, et al. A homozygous deletionmutation in the gene encoding the 180-kDa btllous pemphigoid anti-gen (BPAG2) in a family with generalized atrophic benign epider-molysis bullosa. J Invest Dermatol, 1996,106:771
  • 9[9]McGrath JA, Ishida Yamamoto A, O' Grady A, et al. StructuralVariations in anchoring fibrils in dystrophic epidermolysis bullosa:correlation with type VII collagen expression. J Invest Dermatol,1993,100: 366
  • 10[10].Christiano AM, Morricone A, Paradisi M, et al. A glycine toArginine substitution in the triple-helical domain of type VII colla-gen in a family with dominant dystrophic epidermolysis bullosa. JInvest Dermatol, 1995,104: 438

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