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Epidermolysis bullosa hereditaria

Gespräch mit dem Versorgungsteam des eb-Hauses an der Universitätsklinik für Dermatologie, Paracelsus Medizinische Privatuniversität Salzburg

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Literatur

  1. Nischler E, Klausegger A, Hüttner C et al. Diagnostic pitfalls in newborns and babies with blisters and erosions. (submitted)

  2. Fine JD, Eady RA and Bauer EA et al. (2008). The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB. J Am Acad Dermatol 58: 931–50

    Article  PubMed  Google Scholar 

  3. Mavilio F, Pelegrini G and Ferrari S et al. (2006). Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells. Nat Med 12: 1397–402

    Article  PubMed  CAS  Google Scholar 

  4. Fassihi H, Eady RA and Mellerio JE et al. (2006). Prenatal diagnosis for severe inherited skin disorders: 25 years’ experience. Br J Dermatol 154: 106–13

    Article  PubMed  CAS  Google Scholar 

  5. Ortiz-Urda s, Lin Q, Green CL, Keene DR, Marinkovich MP and Khavari PA. (2003). Injection of genetically engineered fibroblasts corrects regenerated human epidermolysis bullosa skin tissue. J Clin Invest 111: 251–255

    PubMed  CAS  Google Scholar 

  6. Woodley DT, Krueger GG and Jorgensen CM et al. (2003). Normal and gene-corrected dystrophic epidermolysis bullosa fibroblasts alone can produce type VII collagen at the basement membrane zone. J. Invest Dermatol 121: 1021–28

    Article  PubMed  CAS  Google Scholar 

  7. Woodley DT, Remington J and Huang Y et al. (2007). Intravenoulsy injected human fibroblasts home to skin wounds, deliver type VII collagen, and promote wound healing. Mol Ther 15: 628–35

    Article  PubMed  CAS  Google Scholar 

  8. Woodley DT, Keen DR and Atha T. (2004). Intradermal injection of lentiviral vectors corrects regenerated human dystrophic epidermolysis bullosa skin tissue in vivo. Mol Ther 10: 318–26

    Article  PubMed  CAS  Google Scholar 

  9. Woodley DT, Keen DR and Atha T et al. (2004). Injection of recombinant human type VII collagen restores collagen function in dystrophic Epidermolysis bullosa. Nat Med 10: 693–5

    Article  PubMed  CAS  Google Scholar 

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Authors and Affiliations

  1. Interview mit dem Team des eb-Hauses, Salzburg, Österreich

    Martin Laimer &  Helmut Hintner

  2. eb-haus Austria, Universitätsklinik für Dermatologie der Paracelsus Medizinischen Privatuniversität Salzburg, Müllner Hauptstrasse 48, 5020, Salzburg, Österreich

    Helmut Hintner

Authors
  1. Martin Laimer
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  2. Helmut Hintner
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Correspondence to Helmut Hintner.

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Laimer, M., Hintner, H. Epidermolysis bullosa hereditaria. Paediatr. Paedolog. Austria 44, 20–24 (2009). https://doi.org/10.1007/s00608-009-0126-0

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  • DOI: https://doi.org/10.1007/s00608-009-0126-0

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