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Articles by J.W. Bauer
Another twist of the allogenic haematopoietic cell transplantation story
Commentary Another twist of the allogenic haematopoietic cell transplantation story J.W. Bauer, Corresponding Author Department of Dermatology of the Paracelsus Medical University Salzburg, General Hospital Salzburg, Salzburg, Austria Contribution: Conceptualization (lead), Writing - original draft (lead), Writing - review & editing (lead) Search for more papers by this author J.W. Bauer, Corresponding Author Department of Dermatology of the Paracelsus Medical University Salzburg, General...
Expanding the use of allogeneic haematopoietic cell transplantation in dermatology
Commentary PDF ShareShare Abstract Linked Article: Ebens et al. Br J Dermatol 2021; 184:1161–1169. Epidermolysis bullosa (EB) comprises a group of rare, genetically determined skin fragility disorders characterized by (muco)cutaneous blistering following mild mechanical trauma. The most severe clinical symptoms occur in patients affected by mutations in genes coding for type VII collagen and the subchains of laminin 332.
Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility
Summary Background Several new genes and clinical subtypes have been identified since the publication in 2014 of the report of the last International Consensus Meeting on Epidermolysis Bullosa (EB). Objectives We sought to reclassify disorders with skin fragility, with a focus on EB, based on new clinical and molecular data. Methods This was a consensus expert review.
MicroRNAs: one for all, all for one - Wally - - British Journal of Dermatology - Wiley Online Library
Commentary MicroRNAs: one for all, all for one J.W. Bauer Corresponding Author E-mail address: joh.bauer@salk.at Department of Dermatology, University Hospital of the Paracelsus Medical University Salzburg, Austria Correspondence: Johann W. Bauer. E‐mail: joh.bauer@salk.at Search for more papers by this author PDF PDF Share No abstract is available for this article.
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