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J-GLOBAL ID:200902162856519920   Reference number:02A0820439

先天性表皮水ほう症の診断と治療

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Volume: 112  Issue: 10  Page: 1343-1356  Publication year: Sep. 20, 2002 
JST Material Number: Z0668A  ISSN: 0021-499X  CODEN: NHKZAD  Document type: Article
Article type: 文献レビュー  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Dermatlogic diagnosis 
Reference (46):
  • PEARSON, RW. Electron microscopic studies of dermal-epidermal separarion in human skin. J invest Dermatol. 1962, 36, 213-224
  • PEARSON, RW. Studies on the pathogenesis of epidermolysis bullosa. J invest Dermatol. 1962, 39, 551-575
  • DE WEERDT, CF. Her voorkomen van epidermolysis bullosa nereditaria dystrophica en progressieve spiercdstorfie in een gezin. Nederlands Tiidschrift voor Geneeskunde (Amsterdam). 1972, 116, 1264
  • NIEMI, K-M. Epidermolysis bullosa simplex asociated with muscular dystrophy with recessive inheritance. Arch Dermatol. 1988, 124, 551-554
  • HOVNANIAN, A. A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex. Nature Genet. 1993, 3, 327-332
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