Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Ole Swensson"'
Publikováno v:
Contact Dermatitis. 46:253-257
The diagnostic meaningfulness of patch tests with house dust mite allergens is still questionable. Our own impression has been that positive results with a dermatophagoides mix may occur preferentially in patients with a generally enhanced responsive
Autor:
Ole Swensson, B. Swensson, Bernhard Nölle, Rainer Rochels, Hans-Jürgen Thiel, Bernhard Wannke
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 217:43-51
Hintergrund Die Epitheldystrophie Meesmann-Wilke (OMIM 122 100) ist eine seltene autosomal dominant erbliche Erkrankung des Hornhautepithels, die im fruhen Kindesalter nachweisbar ist und beide Augen betrifft. Kennzeichen der Erkrankung ist eine in i
Autor:
Rainer Rochels, Hans-Jürgen Thiel, B Wannke, B. Swensson, L. D. Corden, Whi McLean, Ole Swensson
Publikováno v:
British Journal of Ophthalmology. 84:527-530
AIM—To study a kindred with Meesmann's corneal dystrophy (MCD) to determine if a mutation within the cornea specific K3 or K12 genes is responsible for the disease phenotype. METHODS—Slit lamp examination of the cornea in four members of the kind
Publikováno v:
Experimental Eye Research. 70:41-49
Recently, we identified the first mutations in corneal keratins K3 and K12 in families with Meesmann's corneal dystrophy (MCD). Here, we sequenced all regions of the human K12 gene, to enable mutation detection for all exons using genomic DNA as a te
Autor:
Ole Swensson
Publikováno v:
Der Hautarzt. 50:483-490
Pachyonychia congenita (PC) comprises a heterogeneous group of autosomal dominantly inherited conditions showing characteristic nail thickening and associated signs such as palmoplantar keratoderma, follicular keratoses, and mucosal leukokeratoses. L
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 212:116-119
Background Widespread idiopathic telangiectasia (generalized essential telangiectasia) is a rare skin disorder characterized by the development and gradual spreading of telangiectases. The condition tends to affect women in their midthirties. For no
Publikováno v:
Journal of Investigative Dermatology. 96:682-689
Neutrophil-activating protein-1/interleukin 8 (NAP-1/ IL-8), purified to homogeneity from lipopolysaccharide-stimulated human peripheral blood monocytes, was injected intracutaneously into human skin. Sequential biopsy specimens were taken in order t
Autor:
Fjd Smith, Graeme C.M. Black, Whi McLean, S J Morgan, Alan D. Irvine, J H McCarthy, Johnny Moore, C. M. Coleman, Ole Swensson
Publikováno v:
The British journal of ophthalmology. 86(7)
Background: The molecular basis of Meesmann9s epithelial corneal dystrophy (MECD) has recently been attributed to mutations in the cornea specific keratin genes KRT3 and KRT12. The mechanisms by which these mutations cause the Meesmann9s phenotype ar
Autor:
Jochen, Brasch, Wolfgang, Uter, Maher, Dibo, Eggert, Stockfleth, Ole, Swensson, Enno, Christophers
Publikováno v:
Contact dermatitis. 46(5)
The diagnostic meaningfulness of patch tests with house dust mite allergens is still questionable. Our own impression has been that positive results with a dermatophagoides mix may occur preferentially in patients with a generally enhanced responsive
Autor:
Rainer Rochels, Ole Swensson, Alan D. Irvine, Jo Ellen Moore, RG Knowlton, Jouni Uitto, L. D. Corden, D. G. Frazer, Enno Christophers, B. Swensson, Whi McLean, Fjd Smith
Publikováno v:
Nature genetics. 16(2)
The intermediate filament cytoskeleton of corneal epithelial cells is composed of cornea-specific keratins K3 and K12 (refs 1,2). Meesmann's corneal dystrophy (MCD) is an autosomal dominant disorder causing fragility of the anterior corneal epitheliu