Inherited epidermolysis bullosa comes into the new millenium: A revised classification system based on current knowledge of pathogenetic mechanisms and the clinical, laboratory, and epidemiologic findings of large, well-defined patient cohorts - 11/05/12
Doi : 10.1067/mjd.2000.107739
Jo-David Fine, MD, MPHa,b, John McGrath, MD, FRCPc, Robin A.J. Eady, DSc(Med), FRCPc
Chapel Hill, North Carolina, and London, United Kingdom
From the Departments of Dermatology and Epidemiology,a University of North Carolina at Chapel Hill; The National Epidermolysis Bullosa Registry,b Chapel Hill; and the Department of Cell and Molecular Pathology, St John’s Institute of Dermatology, Guy’s, King’s and St Thomas’ School of Medicine, St Thomas’ Hospital, London.c
 | Reprint requests: Jo-David Fine, MD, MPH, Department of Dermatology, University of North Carolina at Chapel Hill, Thurston-CB #7287, Chapel Hill, NC 27599-7287. |
| J Am Acad Dermatol 2000;43:135-7. |
© 2000
American Academy of Dermatology, Inc. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 43 - N° 1P1
P. 135-137 - juillet 2000 Retour au numéro
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