Results 101 to 110 of about 406 (136)

Schnyder Crystalline Corneal Dystrophy

open access: yes, 2009
Alexander K. C. Leung   +150 more
exaly   +3 more sources

Central Crystalline Corneal Dystrophy of Schnyder

open access: yes, 2009
Nils Peters   +199 more
exaly   +3 more sources

High expression of Matrix Gla Protein in Schnyder corneal dystrophy patients points to an active role of vitamin K in corneal health

open access: yesActa Ophthalmologica, 2021
Purpose Schnyder corneal dystrophy (SCD) is a rare autosomal dominant disorder characterized by corneal lipid accumulation and caused byUBIAD1pathogenic variants.UBIAD1encodes a vitamin K (VK) biosynthetic enzyme.
Anna Sarosiak   +2 more
exaly   +2 more sources
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HEREDITARY CRYSTALLINE CORNEAL DYSTROPHY OF SCHNYDER

Acta Ophthalmologica, 1973
A family with three members affected by hereditary crystalline corneal dystrophy of Schnyder is reported. Penetrating keratoplasty was performed in two of the affected members. Clear grafts were obtained. The buttons were examined by light‐ and electronmicroscopy. The epithelium was normal.
Niels Ehlers, M E Matthiessen
exaly   +3 more sources

Panstromal Schnyder's Corneal Dystrophy

Ophthalmology, 1992
Merlyn M Rodrigues   +2 more
exaly   +2 more sources

Panstromal Schnyder Corneal Dystrophy

Ophthalmology, 1994
Sheila Innis, Valerie White
exaly   +2 more sources

Progressive Schnyder's Corneal Dystrophy

Ophthalmology, 1993
Schnyder's crystalline dystrophy is a central anterior bilateral corneal dystrophy characterized by the deposition of crystals composed of cholesterol and other lipids. This condition classically is described as nonprogressive after childhood, but a series of recent studies following patients over time has challenged this teaching.The authors present a
H J, Ingraham   +3 more
openaire   +2 more sources

Genetic analysis of 14 families with Schnyder crystalline corneal dystrophy reveals clues to UBIAD1 protein function

open access: yesAmerican Journal of Medical Genetics, Part A, 2008
Howard S Kruth   +2 more
exaly   +2 more sources

Central Corneal Mosaic Opacities in Schnyder's Crystalline Dystrophy

Ophthalmology, 2005
To report an unusual presentation of Schnyder's corneal crystalline dystrophy (SCCD), sharing the feature of central corneal mosaic opacities.Observational case report.A 51-year-old man and his family members were examined. Investigations included slit-lamp biomicroscopy, radiography of knee joint, plasma lipid level, and genotyping of the SCCD ...
Chih-Wei Wu   +2 more
exaly   +3 more sources

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