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Skin Pharmacology and Applied Skin Physiology|November 5, 1999
Alterations of rat liver phospholipid composition induced by oral thalidomideA Kalofoutis, A Monastirli, A Papapanagiotou, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 1, 1986
[Clinical aspects of progressive systemic scleroderma (PSS). Multicenter studies of 194 patients]G Goerz, G Hammer, G Wirth, et al.Annals of Human Genetics|November 6, 1998
C73R is a hotspot mutation in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyriaJ Frank, X Wang, H M Lam, et al.Human Genetics|January 1, 1997
Molecular basis of variegate porphyria: a de novo insertion mutation in the protoporphyrinogen oxidase geneH Lam, L Dragan, H C Tsou, et al.Journal of the American Academy of Dermatology|June 1, 1997
High-dose UVA1 radiation therapy for localized sclerodermaH Stege, M Berneburg, S Humke, et al.Journal of Cell Science|May 12, 1998
Psoralen photoactivation promotes morphological and functional changes in fibroblasts in vitro reminiscent of cellular senescenceG Herrmann, P Brenneisen, M Wlaschek, et al.The Journal of Investigative Dermatology|January 1, 1992
Migration of a human keratinocyte cell line (HACAT) to interstitial collagen type I is mediated by the alpha 2 beta 1-integrin receptorK Scharffetter-Kochanek, C E Klein, G Heinen, et al.Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|August 4, 1999
Erythropoietic protoporphyria: identification of novel mutations in the ferrochelatase gene and comparison of biochemical markers versus molecular analysis as diagnostic strategiesJ Frank, J Nelson, X Wang, et al.Pageof 19