Immunohistochemical Observation of Proteoglycans in Albopapular Lesions in the Pasini Form of Dystrophic Epidermolysis Bullosa.
Author:
Publisher
Western Japan Division of JDA
Subject
Dermatology
Reference14 articles.
1. Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa
2. 2) Sasai Y, Saito N, Seiji M: Epidermolysis bullosa dystrophica et albo-papuloidea. Arch Dermatol 108: 554-557, 1973.
3. 3) Endo M et al: Urinary chondroitin of epidermolysis bullosa dystrophica et albo-papuloidea (Pasini). Clin Chim Acta 67: 249-253, 1974.
4. 4) Bauer EA, Fiehler WK, Esterly NB: Increased glycosaminoglycan accumulation as a genetic characteristic in cell cultures of one variety of dominant dystrophic epidermolysis bullosa. J Clin Invest 64: 32-39, 1979.
5. 5) Scott JE, Dorling J: Differential staining of acid glycosamino-glycans (mucopolysaccharides) by alcian blue in salt solutions. Histochemie 5: 221-233, 1965.
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