1. Allman, S., Haynes L., MacKinnon, P., Atherton, D.J. (1992) Nutrition in dystrophic epidermolysis bullosa. Pediatric Dermatology. 9 (3): 231-238

  2. Bauer, E.A., Herron, G.S., Marinkovich, M.P., Khavari, P.A., Lane A.T. (1999) Gene therapy for a lethal genetic blistering disease: a status report. Transactions of the American Clinical and Climatological Association. 110: 86-92.

  3. Chiu, Y., Prendiville, J.S., Bennett, S.M., Psych, R., Montgomery, C.J., Oberlander, T.F. (1999) Pain management of junctional epidermolysis bullosa in an 11-year-old boy. Pediatric Dermatology 16 (6): 465-468.

  4. Fine J, Bauer, E.A., McGuire J., Moshell, A. Eds (1999) Epidermolysis Bullosa: Clinical, Epidemiologic, and Laboratory Advance and the Findings of the National Epidermolysis Bullosa Registry . The John Hopkins University Press. Maryland.

  5. Goldstein, A.M., Davenport, T., Sheridan, R.L. (1998) Junctional Epidermolysis Bullosa: Diagnosis and Management of a patient with the herlitz variant. Journal of Pediatric Surgery. 33 (5): 756-758.

  6. Haynes, L. (1998) Nutritional support for children with epidermolysis bullosa. Journal of Human Nutrition and Dietetics. 11: 163-173.

  7. Haynes, L., Atherton D.J., Clayden, G. (1997) Constipation in Epidermolysis Bullosa: Successful treatment with a liquid fiber-containing formula. Pediatric Dermatology. 14 (5): 393-396.

  8. Haynes, L., Atherton D.J., Ade-Ajayi N., Wheeler R., Kiely E.M. (1996) Gastrostomy and growth in dystrophic epidermolysis bullosa. British Journal of Dermatology. 134: 872-879.

  9. Khavari, P.A. (1998) Gene therapy for genetic skin disease. The Journal of Investigative Dermatology. 110 (4): 462-467.

  10. Lim, K.K., Su, W.P.D., McEvoy, M.T., Pittelkow, M.R. (1996) Generalized gravis junctional Epidermolysis Bullosa: case report, laboratory evaluation, and review of recent advances. Mayo Clinic Proc. Sept, Vol 71: 863-868.

  11. Marinkovich, M.P. (1999) Update on inherited bullous dermatoses. Dermatologic Clinics 17 (3): 473-485.

  12. McLean, W.H., Pulkkinen, L., Smith, F.J.D., Rugg, E.L., Lane, E.B., Bullrich, F., Burgeson, R.E., Amano, S., Hudson, D.L., Owarive, K., McGrath, J.A., McMillan, J.R., Eady, R.A.J., Leigh, I.M., Christiano, A.M., Uitto, J. (1996) Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization. Genes and Development 10: 1724-1735.

  13. Mellerio, J.E. (1999) Molecular pathology of the cutaneous basement membrane zone. Experimental Dermatology Review Article 24:25-32.

  14. Puvabanditsin, S., Garrow, E., Samransamraujkit, R., Lopez, L. A., Lambert, W.C. (1997) Epidermolysis Bullosa associated with congenital localized absence of skin, fetal abdominal mass, and pyloric atresia. Pediatric Dermatology 14 (5): 359-362.

  15. Uitto, J. (1999) Molecular diagnostics of epidermolysis bullosa: novel pathomechanisms and surprising genetics. Experimental Dermatology. 8: 92-95.

The Queensland branch of DEBRA-A is pleased to be a resource of information about EB. However, the information provided here should never take the place of advice from your health care provider. Be sure to check with your health care provider about any changes in your treatment plan.