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Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|November 6, 2015
[Practical aspects of molecular diagnostics in genodermatoses]C Has, Y HeDer Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|January 29, 2011
[Epidermolysis bullosa : Diagnosis and therapy]C Has, L Bruckner-TudermanEuropean Journal of Dermatology : EJD|August 30, 2001
Resurfacing CO2 laser treatment of linear verrucous epidermal nevusJ L Michel, C Has, V HasCell Motility and the Cytoskeleton|November 15, 2007
Novel interaction partners of Bardet-Biedl syndrome proteinsF Oeffner, C Moch, A Neundorf, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|September 2, 2004
[Hereditary blistering disorders]C Has, J S Kern, L Bruckner-TudermanClinical and Experimental Dermatology|March 19, 2014
Kindler syndrome with severe mucosal involvement in childhoodC V Krishna, N V Parmar, C HasJournal of Neurology, Neurosurgery, and Psychiatry|May 15, 2008
Novel TOR1A mutation p.Arg288Gln in early-onset dystonia (DYT1)B Zirn, K Grundmann, P Huppke, et al.Clinical Genetics|December 24, 2010
Ring chromosome 22 and neurofibromatosis type II: proof of two-hit model for the loss of the NF2 gene in the development of meningiomaB Zirn, L Arning, I Bartels, et al.Case Reports in Dermatology|September 11, 2013
Acral peeling skin syndrome resembling epidermolysis bullosa simplex in a 10-month-old boyS Kavaklieva, I Yordanova, L Bruckner-Tuderman, et al.The British Journal of Dermatology|June 21, 2008
Dystrophic epidermolysis bullosa pruriginosa is not associated with frequent FLG gene mutationsH Schumann, C Has, J Kohlhase, et al.Pageof 10