Výsledky vyhledávání

Fernmetastasen durch Plattenepithelkarzinom der Bindehaut

Publikováno v: Klinische Monatsblätter für Augenheilkunde. 219:813-816

Background: Squamous cell carcinoma of the conjunctiva is rare. Together with epithelial dysplasia of the conjunctiva the incidence is reported to be 1.9 per 100 000 population and year. After adequate therapy total cure is often achieved. Generalise

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1e6b0c2c9899e8230543211eaa41b21f
https://doi.org/10.1055/s-2002-36326

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Keratin-Gen-Mutationen als Ursache der Epitheldystrophie Meesmann-Wilke und autosomal dominanter Verhornungsstörungen der Haut1

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::74712c40ddcf49073942fb006ec27b6d
https://doi.org/10.1055/s-2000-10382

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A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b382d69a48a1d9894627137a63a4770
https://doi.org/10.1136/bjo.84.5.527

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Molecular Genetics of Meesmann's Corneal Dystrophy: Ancestral and Novel Mutations in Keratin 12 (K12) and Complete Sequence of the Human KRT12 Gene

Autor: L. D. Corden, B. Swensson, Jouni Uitto, Rainer Rochels, Ole Swensson, Whi McLean, Fjd Smith

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41849e159f41a0e00d4c407ae56f3053
https://doi.org/10.1006/exer.1999.0769

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Progressive disseminierte essentielle Teleangiektasien mit konjunktivaler Beteiligung

Autor: B. Swensson, Georg Häring, Ole Swensson

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::076246a71eaf3e2803121ecaf59e3b53
https://doi.org/10.1055/s-2008-1034844

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Akademický článek

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

Autor: O, Swensson, B, Swensson, B, Nölle, R, Rochels, B, Wannke, H J, Thiel

Publikováno v: Klinische Monatsblatter fur Augenheilkunde. 217(1)

Meesmann's corneal dystrophy (OMIM 122,100) is a rare autosomal dominant disorder of the corneal epithelium. It manifests in early childhood and affects both eyes. The disease is characterized by variable patterned dot-like corneal opacities and intr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::82772245aeb200dfeed90d57c1d523b3
https://pubmed.ncbi.nlm.nih.gov/10949816

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Posterior Subcapsular Cataract and Dry Eye Syndrome after Radiation Exposure by the Chernobyl Accident

Autor: R. U. Peter, B. Swensson, F. H. Stefani, A. K. Junk, P. Egner, A. M. Kellerer

Publikováno v: Ocular Radiation Risk Assessment in Populations Exposed to Environmental Radiation Contamination ISBN: 9789401062213
Ocular Radiation Risk Assessment in Populations Exposed to Environmental Radiation Contamination

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::31697481f74687eab342318dfba50918
https://doi.org/10.1007/978-94-011-5278-5_5

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[Progressive disseminated essential telangiectasia with conjunctival involvement]

Autor: B, Swensson, O, Swensson, G, Häring

Publikováno v: Klinische Monatsblatter fur Augenheilkunde. 212(2)

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 apparent re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fa161f8ad52095ce0c5b129071aa1643
https://pubmed.ncbi.nlm.nih.gov/9577812

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