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Epidermolysis Bullosa Simplex

Keywords

Bullous Pemphigoid Epidermolysis Bullosa Lamina Densa Suprabasal Cell Keratin Filament 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Chan Y, Yu Q, Fine J, and Fuchs E (1993) The genetic basis of Weber-Cockayne epidermolysis bullosa simplex. Proc Natl Acad Sci USA 90: 7414PubMedGoogle Scholar
  2. Eady R, McGrath J, and McMillan J (1994) Ultrastructural clues to genetic disorders of the skin: the dermal-epidermal junction. J Invest Dermatol 103: 13SCrossRefPubMedGoogle Scholar
  3. Fuchs E (2001) Disorders of intermediate filaments and their associated proteins. In: The metabolic and metabolic bases of inherited disease (Scriver C, Beaudet A, Valle D, and Sly WS, eds). New York: McGraw-Hill, pp 5629Google Scholar
  4. Ishida-Yamamota A, Mc Grath J, Chapman S, Leigh I, Lane E, and Eady R (1991) Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterised by abnormal keratin-filament network involving keratins K5 and K14. J Invest Dermatol 97: 959CrossRefPubMedGoogle Scholar
  5. Letai A, Coulombe P, McCormick M, Yu Q, Hutton E, and Fuchs E (1993) Disease severity correlates with position of keratin point mutations in epidermolysis bullosa simplex. Proc Natl Acad Sci USA 90: 3197PubMedGoogle Scholar
  6. Pearson R, and Spargo B (1961) Electron microscope studies of dermal-epidermal separation in human skin. J Invest Dermatol 36: 213PubMedGoogle Scholar
  7. Uitto J, and Pulkinnen L (2001) Epidermolysis bullosa: the disease of the cutaneous basement membrane zone. In: The metabolic and metabolic bases of inherited disease (Scriver C, Beaudet A, Valle D, and Sly W, eds). New York: McGraw-Hill, pp 5655Google Scholar
  8. Wilgram G, and Caulfield J (1966) An electron microscopic study of epidermolytic hyperkeratosis. Arch Dermatol 94: 127CrossRefPubMedGoogle Scholar

Copyright information

© Springer-Verlag/Wien 2005

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