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Results: 1-9 |
Results: 9
Keratin gene mutations cause Meesmann's corneal dystrophy and autosomal dominant skin disorders of cornification
Authors: Swensson, O Swensson, B Nolle, B Rochels, R Wannke, B Thiel, HJ
Citation: O. Swensson et al., Keratin gene mutations cause Meesmann's corneal dystrophy and autosomal dominant skin disorders of cornification, KLIN MONATS, 217(1), 2000, pp. 43-51
Molecular genetics of Meesmann's corneal dystrophy: Ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene
Authors: Corden, LD Swensson, O Swensson, B Smith, FJD Rochels, R Uitto, J McLean, WHI
Citation: Ld. Corden et al., Molecular genetics of Meesmann's corneal dystrophy: Ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene, EXP EYE RES, 70(1), 2000, pp. 41-49
A novel keratin 12 mutation in a German kindred wi th Meesmann's corneal dystrophy
Authors: Corden, LD Swensson, O Swensson, B Rochels, R Wannke, B Thiel, HJ McLean, WHI
Citation: Ld. Corden et al., A novel keratin 12 mutation in a German kindred wi th Meesmann's corneal dystrophy, BR J OPHTH, 84(5), 2000, pp. 527-530
Association of lymphocytic colitis with linear IgA dermatosis
Authors: Stuber, E Swensson, O Nitsche, R Nickel, T Sticherling, M Christophers, E Folsch, UR
Citation: E. Stuber et al., Association of lymphocytic colitis with linear IgA dermatosis, Z GASTROENT, 37(6), 1999, pp. 519-523
Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-senseor frameshift mutations
Authors: McGrath, JA Ashton, GHS Mellerio, JE Salas-Alanis, JC Swensson, O McMillan, JR Eady, RAJ
Citation: Ja. Mcgrath et al., Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-senseor frameshift mutations, J INVES DER, 113(3), 1999, pp. 314-321
Pachyonychia congenita. Keratin gene mutations with pleiotropic effect
Authors: Swensson, O
Citation: O. Swensson, Pachyonychia congenita. Keratin gene mutations with pleiotropic effect, HAUTARZT, 50(7), 1999, pp. 483-490
Comel-Netherton syndrome complicated by papillomatous skin lesions containing human papillomaviruses 51 and 52 and plane warts containing human papillomavirus 16
Authors: Folster-Holst, R Swensson, O Stockfleth, E Monig, H Mrowietz, U Christophers, E
Citation: R. Folster-holst et al., Comel-Netherton syndrome complicated by papillomatous skin lesions containing human papillomaviruses 51 and 52 and plane warts containing human papillomavirus 16, BR J DERM, 140(6), 1999, pp. 1139-1143
Paraneoplastic bullous pemphigoid resembling erythema gyratum repens
Authors: Hauschild, A Swensson, O Christophers, E
Citation: A. Hauschild et al., Paraneoplastic bullous pemphigoid resembling erythema gyratum repens, BR J DERM, 140(3), 1999, pp. 550-552
Linear IgA disease associated with lymphocytic colitis
Authors: Swensson, O Stuber, E Nickel, T Sticherling, M Ghohestani, RF Nitsche, R Christophers, E
Citation: O. Swensson et al., Linear IgA disease associated with lymphocytic colitis, BR J DERM, 140(2), 1999, pp. 317-321
Risultati: 1-9 |