J. W. Bauer

发表

Clinical trial of ABCB5 + mesenchymal stem cells for recessive dystrophic epidermolysis bullosa

J. Tolar, C. Ebens, A. Hovnanian, 2021 .

Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification.

E. Bauer, H. Shimizu, J. Uitto, 2014, Journal of the American Academy of Dermatology.

Large melanocytic nevi in hereditary epidermolysis bullosa.

J. Bauer, H. Schaeppi, H. Hintner, 2001, Journal of the American Academy of Dermatology.

Premature termination codons are present on both alleles of the bullous pemphigoid antigen 2/type XVII collagen gene in five Austrian families with generalized atrophic benign epidermolysis bullosa.

J. Uitto, J. McGrath, A. Christiano, 1997, The Journal of investigative dermatology.

Matrix metalloproteinase‐7 activates heparin‐binding epidermal growth factor‐like growth factor in cutaneous squamous cell carcinoma

J. McGrath, R. Grenman, R. Ala-aho, 2010, The British journal of dermatology.

Autoimmune bullous diseases in Austria.

V. Ahlgrimm-Siess, M. Laimer, J. Bauer, 2011, Dermatologic clinics.

A localized variant of paraneoplastic pemphigus: acantholysis associated with malignant melanoma

D. Metze, J. Bauer, W. Salmhofer, 2001, The British journal of dermatology.

Dystrophic Epidermolysis Bullosa

M. Laimer, J. Bauer, H. Hintner, 2015 .

Molecular epidemiology of junctional epidermolysis bullosa: discovery of novel and frequent LAMB3 mutations in Chilean patients with diagnostic significance

G. Repetto, S. González, A. Klausegger, 2017, The British journal of dermatology.