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Klinische Monatsblatter Fur Augenheilkunde|May 13, 1998
[Progressive disseminated essential telangiectasia with conjunctival involvement]B Swensson, O Swensson, G HäringKlinische Monatsblatter Fur Augenheilkunde|August 19, 2000
[Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]O Swensson, B Swensson, B Nölle, et al.Experimental Eye Research|January 25, 2000
Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 geneL D Corden, O Swensson, B Swensson, et al.The British Journal of Ophthalmology|April 27, 2000
A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophyL D Corden, O Swensson, B Swensson, et al.Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|August 28, 1999
[Pachyonychia congenita. Keratin gene mutations with pleiotropic effect]O SwenssonArchives of Dermatology|March 6, 1998
Generalized atrophic benign epidermolysis bullosa in 2 siblings complicated by multiple squamous cell carcinomasO Swensson, E ChristophersArchives of Dermatological Research|February 1, 1996
Morphology of the keratin filament network in palm and sole skin: evidence for site-dependent features based on stereological analysisO Swensson, R A EadyNature Genetics|June 1, 1997
Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophyA D Irvine, L D Corden, O Swensson, et al.Archives of Dermatological Research|January 1, 1989
Transendothelial cell diapedesis of neutrophils in inflamed human skinC Schubert, E Christophers, O Swensson, et al.The Journal of Investigative Dermatology|May 1, 1991
Inflammatory properties of neutrophil-activating protein-1/interleukin 8 (NAP-1/IL-8) in human skin: a light- and electronmicroscopic studyO Swensson, C Schubert, E Christophers, et al.Pageof 4