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Experimental Dermatology|October 12, 2020
Translational perspectives to treat Epidermolysis bullosa-Where do we stand?Christine Prodinger, Johann W Bauer, Martin LaimerJournal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|October 30, 2015
Hereditary epidermolysis bullosaMartin Laimer, Christine Prodinger, Johann W BauerExperimental Dermatology|May 30, 2019
Epidermolysis bullosa: Advances in research and treatmentChristine Prodinger, Julia Reichelt, Johann W Bauer, et al.Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|August 11, 2020
EB (epidermolysis bullosa)-House Austria: Pioneering work for the care of patients with rare diseasesChristine Prodinger, Martin Laimer, Johann W Bauer, et al.Wiener Klinische Wochenschrift|December 3, 2016
Epidermolysis bullosa House Austria and Epidermolysis bullosa clinical network : Example of a centre of expertise implemented in a European reference network to face the burden of a rare diseaseMartin Laimer, Gabriela Pohla-Gubo, Anja Diem, et al.BMC Pregnancy and Childbirth|December 16, 2025
Patient-reported outcomes during pregnancy and delivery in epidermolysis bullosaAnna Zott, Anja Diem, Christine Prodinger, et al.Expert Opinion on Biological Therapy|September 1, 2004
Gene therapy of epidermolysis bullosaJohann W Bauer, Martin LaimerDermatology and Therapy|June 10, 2021
Clinical Perspectives of Gene-Targeted Therapies for Epidermolysis BullosaTobias Welponer, Christine Prodinger, Josefina Pinon-Hofbauer, et al.Orphanet Journal of Rare Diseases|July 12, 2020
Profiling trial burden and patients' attitudes to improve clinical research in epidermolysis bullosaChristine Prodinger, Anja Diem, Katherina Ude-Schoder, et al.Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|March 7, 2025
Complicated and deep bacterial skin and soft tissue infectionsChristine Prodinger, Arno Lechner, Arno Hintersteininger, et al.Pageof 17