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Dermatologica|January 1, 1988
Lack of type VII collagen in unaffected skin of patients with severe recessive dystrophic epidermolysis bullosaL Bruckner-Tuderman, S Rüegger, B Odermatt, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1987
[Congenital nevus cell nevi as precursors of melanomas of the skin]U W Schnyder, B V Schneider, O Maie, et al.Archives for Dermatological Research = Archiv Fur Dermatologische Forschung|August 27, 1976
Ultrastructural studies in epidermolysis bullosa hereditaria. III. Recessive dystrophic types with dermolytic blistering (Hallopeau-Siemens types and inverse type)I Hashimoto, U W Schnyder, I Anton-Lamprecht, et al.The British Journal of Dermatology|March 1, 1990
Type VII collagen is expressed but anchoring fibrils are defective in dystrophic epidermolysis bullosa inversaL Bruckner-Tuderman, K M Niemi, M Kero, et al.Survey of Ophthalmology|June 27, 2001
A. Franceschetti--great ophthalmologist and humanitarianA Schlossman, A FranceschettiArchives of Dermatological Research|January 1, 1987
Cryofibrinogenemic purpuraA Brüngger, M Brülisauer, Y Mitsuhashi, et al.Dermatologica|April 1, 1982
Rapid laboratory diagnostic of X-linked ichthyosisJ C Meyer, V Groh, V Giger, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|February 1, 1982
[Systemic cutis laxa-like pseudoxanthoma elasticum]H Schibli, S B Stutz, A Vogel, et al.Journal of the American Academy of Dermatology|August 1, 1989
Epidermolysis bullosa simplex with mottled pigmentationL Bruckner-Tuderman, A Vogel, S Rüegger, et al.The Journal of Investigative Dermatology|November 11, 1992
Anchoring fibrils, collagen VII, and neutral metalloproteases in recessive dystrophic epidermolysis bullosa inversaL Bruckner-Tuderman, J O Winberg, I Anton-Lamprecht, et al.Pageof 11