Swensson O[au] - Search Results

Year	Number of Results
1989	1
1991	1
1993	1
1995	2
1996	2
1997	1
1998	3
1999	6
2000	3
2002	2
2006	1
2024	0

1

[Pachyonychia congenita. Keratin gene mutations with pleiotropic effect].

Swensson O. Swensson O. Hautarzt. 1999 Jul;50(7):483-90. doi: 10.1007/s001050050947. Hautarzt. 1999. PMID: 10464680 Review. German.

2

Paraneoplastic bullous pemphigoid resembling erythema gyratum repens.

Hauschild A, Swensson O, Christophers E. Hauschild A, et al. Among authors: swensson o. Br J Dermatol. 1999 Mar;140(3):550-2. doi: 10.1046/j.1365-2133.1999.02736.x. Br J Dermatol. 1999. PMID: 10233292 Review. No abstract available.

3

[Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders].

Swensson O, Swensson B, Nölle B, Rochels R, Wannke B, Thiel HJ. Swensson O, et al. Klin Monbl Augenheilkd. 2000 Jul;217(1):43-51. doi: 10.1055/s-2000-10382. Klin Monbl Augenheilkd. 2000. PMID: 10949816 Review. German.

4

Keratin 16 and keratin 17 mutations cause pachyonychia congenita.

McLean WH, Rugg EL, Lunny DP, Morley SM, Lane EB, Swensson O, Dopping-Hepenstal PJ, Griffiths WA, Eady RA, Higgins C, et al. McLean WH, et al. Among authors: swensson o. Nat Genet. 1995 Mar;9(3):273-8. doi: 10.1038/ng0395-273. Nat Genet. 1995. PMID: 7539673

5

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy.

Irvine AD, Corden LD, Swensson O, Swensson B, Moore JE, Frazer DG, Smith FJ, Knowlton RG, Christophers E, Rochels R, Uitto J, McLean WH. Irvine AD, et al. Among authors: swensson o. Nat Genet. 1997 Jun;16(2):184-7. doi: 10.1038/ng0697-184. Nat Genet. 1997. PMID: 9171831

6

Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress.

Swensson O, Langbein L, McMillan JR, Stevens HP, Leigh IM, McLean WH, Lane EB, Eady RA. Swensson O, et al. Br J Dermatol. 1998 Nov;139(5):767-75. doi: 10.1046/j.1365-2133.1998.02499.x. Br J Dermatol. 1998. PMID: 9892940

7

Gene targeting at the mouse cytokeratin 10 locus: severe skin fragility and changes of cytokeratin expression in the epidermis.

Porter RM, Leitgeb S, Melton DW, Swensson O, Eady RA, Magin TM. Porter RM, et al. Among authors: swensson o. J Cell Biol. 1996 Mar;132(5):925-36. doi: 10.1083/jcb.132.5.925. J Cell Biol. 1996. PMID: 8603923 Free PMC article.

8

[Progressive disseminated essential telangiectasia with conjunctival involvement].

Swensson B, Swensson O, Häring G. Swensson B, et al. Among authors: swensson o. Klin Monbl Augenheilkd. 1998 Feb;212(2):116-9. doi: 10.1055/s-2008-1034844. Klin Monbl Augenheilkd. 1998. PMID: 9577812 German.

9

Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratoderma.

Navsaria HA, Swensson O, Ratnavel RC, Shamsher M, McLean WH, Lane EB, Griffiths D, Eady RA, Leigh IM. Navsaria HA, et al. Among authors: swensson o. J Invest Dermatol. 1995 Mar;104(3):425-9. doi: 10.1111/1523-1747.ep12666011. J Invest Dermatol. 1995. PMID: 7532198 Free article.

10

Inflammatory properties of neutrophil-activating protein-1/interleukin 8 (NAP-1/IL-8) in human skin: a light- and electronmicroscopic study.

Swensson O, Schubert C, Christophers E, Schröder JM. Swensson O, et al. J Invest Dermatol. 1991 May;96(5):682-9. doi: 10.1111/1523-1747.ep12470606. J Invest Dermatol. 1991. PMID: 2022875 Free article.

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