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Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|April 1, 1992
[Typing of infiltration cells in primary, localized, nodular, cutaneous amyloidosis]N Sepp, K Grünewald, H P Soyer, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|April 29, 1998
[Hereditary angioedema in the German-speaking region]H D Göring, K Bork, P J Späth, et al.The British Journal of Dermatology|July 21, 2005
Epidermolysis bullosa naevi reveal a distinctive dermoscopic patternC M Lanschuetzer, M Emberger, M Laimer, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|April 29, 2006
Introducing a fast and simple PCR-RFLP analysis for the detection of mutant thiopurine S-methyltransferase alleles TPMT*3A and TPMT*3CK Oender, C M Lanschuetzer, M Laimer, et al.The Journal of Investigative Dermatology|October 1, 1991
Gene rearrangement studies in the diagnosis of primary systemic and nodular primary localized cutaneous amyloidosisK Grünewald, N Sepp, K Weyrer, et al.Experimental Dermatology|August 1, 1995
Diminished expression of the extracellular domain of bullous pemphigoid antigen 2 (BPAG2) in the epidermal basement membrane of patients with generalized atrophic benign epidermolysis bullosaG Pohla-Gubo, Z Lazarova, G J Giudice, et al.Journal of the American Academy of Dermatology|February 1, 1997
Intravenous immunoglobulin treatment in therapy-resistant epidermolysis bullosa acquisitaH Kofler, B Wambacher-Gasser, G Topar, et al.Assay and Drug Development Technologies|January 4, 2007
Relative quantitation of protein-protein interaction strength within the yeast two-hybrid system via fluorescence beta-galactosidase activity detection in a high-throughput and low-cost mannerK Oender, P Niedermayr, H Hintner, et al.The British Journal of Dermatology|May 15, 2008
Nonsense-associated altered splicing of the Patched gene fails to suppress carcinogenesis in Gorlin syndromeM Laimer, K Onder, P Schlager, et al.Journal of Cutaneous Pathology|September 26, 2003
Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorderC M Lanschuetzer, W H Muss, M Emberger, et al.Pageof 70