Aktuelle Dermatologie 2010; 36(1/02): 43-59
DOI: 10.1055/s-2008-1077743
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© Georg Thieme Verlag KG Stuttgart · New York

Epidermolysis bullosa hereditaria

Epidermolysis Bullosa HereditariaM.  Laimer1 , J.  W.  Bauer1 , C.  M.  Lanschützer1 , E.  Nischler1 , H.  Hintner1
  • 1Universitätsklinik für Dermatologie, Paracelsus Medizinische Privatuniversität (PMU) Salzburg, Salzburger Landeskliniken (SALK)
Further Information

Publication History

Publication Date:
19 May 2009 (online)

Prof. Dr. Helmut Hintner

Literatur

  • 1 Fine J D, Eady R A, Bauer E A. et al . The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB.  J Am Acad Dermatol.. 2008;  58 931-950
  • 2 Fine J D, Hintner H. Life with Epidermolysis Bullosa (EB): Etiology, diagnosis, multidisciplinary care and therapy. Springer Wien; 2008:
  • 3 Mellerio J E, Pulkkinen L, McMillan J R. et al . Pyloric atresia-junctional epidermolysis bullosa syndrome: mutations in the integrin beta4 gene (ITGB4) in two unrelated patients with mild disease.  Br J Dermatol. 1998;  139 862-871
  • 4 Lanschuetzer C M, Emberger M, Laimer M. et al . Epidermolysis bullosa naevi reveal a distinctive dermoscopic pattern.  Br J Dermatol. 2005;  153 97-102
  • 5 Fine J D, Johnson L B, Suchindran C. et al .Cutaneous and skin-associated musculoskeletal manifestations of inherited EB: the National Epidermolysis Bullosa Registry Experience. In: Fine JD, Bauer EA, McGuire J, Moshell A (eds) Epidermolysis bullosa: clinical, epidemiologic, and laboratory advances, and the findings of the National Epidermolysis Bullosa Registry. Baltimore; Johns Hopkins University Press 1999:
  • 6 Hintner H, Wolff K. Generalized atrophic benign epidermolysis bullosa.  Arch Dermatol. 1982;  118 375-384
  • 7 Hintner H, Stingl G, Schuler G. et al . Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in the mechanobullous diseases.  J Invest Dermatol. 1981;  76 113-118
  • 8 Mavilio F, Pellegrini G, Ferrari S. et al . Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells.  Nat Med. 2006;  12 1397-1402
  • 9 Bauer J W, Laimer M. Gene therapy of epidermolysis bullosa.  Expert Opin Biol Ther. 2004;  4 1435-1443
  • 10 Woodley D T, Keen D R, Atha T. et al . Injection of recombinant human type VII collagen restores collagen function in dystrophic Epidermolysis bullosa.  Nat Med. 2004;  10 693-695
  • 11 Woodley D T, Remington J, Huang Y. et al . Intravenoulsy injected human fibroblasts home to skin wounds, deliver type VII collagen, and promote wound healing.  Mol Ther. 2007;  15 628-635

Prof. Dr. Helmut Hintner

Universitätsklinik für Dermatologie
Paracelsus Medizinische Privatuniversität (PMU) Salzburg
Salzburger Landeskliniken (SALK)

Müllner Hauptstraße 48
A-5020 Salzburg
Österreich

Email: h.hintner@salk.at