Results 51 to 60 of about 406 (136)

2019 ACVIM Forum Research Abstract Program

, 2019
Journal of Veterinary Internal Medicine, Volume 33, Issue 5, Page 2375-2547, September/October 2019.
wiley   +1 more source

IC³D-Klassifikation von Hornhautdystrophien

, 2011
Background: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification.
B. Seitz, A. Aldave, C. Bredrup, T. Kivelä, H. Møller, E. Kim, G. Klintworth, Lisch, W., Kinoshita, S., W. Lisch, Aldave, A. J., J. Weiss, F. Munier, Mannis, M. J., Munier, F. L., Bredrup, C., Klintworth, G. K., G. Rij, J. Sutphin, Rapuano, C., M. Mannis, Mà ̧ller, H. U., Belin, M. W., C. Rapuano, M. Belin, M. Busin, Seitz, B., Busin, M., Sutphin, J., Kim, E. K., Rij, G. Van., Weiss, J. S., Kivelä, T., S. Kinoshita   +33 more
core   +1 more source

In vivo confocal microscopy as a diagnostic tool in Schnyder Corneal Dystrophy’s case

, 2019
Schnyder’s corneal dystrophy (SCD) is a rare corneal condition characterized by cholesterol and phospholipids deposition in the stroma and Bowman’s layer. We present a case report of a patient who had a progressive corneal stromal haze in both eyes since
Débora Biazim (7234802), Paula Kataguiri (7234808), Diego Casagrande (7234805)   +2 more
core   +1 more source

Stromal corneal dystrophy (possible Schnyder’s dystrophy) with peripheral corneal degeneration – diagnostic and therapeutic challenges

Romanian Journal of Ophthalmology, 2018
Purpose: to highlight the diagnostic and therapeutic challenges in a case with central and peripheral corneal lesions. Methods: We present the preoperative investigations: anterior segment optical coherence tomography and ultrasound biomicroscopy; The excised cornea has been examined histopathologically.
Mihail, Zemba, Raluca, Neacsa, Bogdan Ion, Cucu   +2 more
openaire   +2 more sources

Schnyder’s crystalline corneal dystrophy [PDF]

QJM: An International Journal of Medicine, 2019
S Handa, A Thakur, D Rajneesh, A Kulshrestha, A Gupta   +4 more
openaire   +2 more sources

Distrofia de Schnyder

Revista Cubana de Oftalmología
Entre las distrofias estromales encontramos la distrofia de Schnyder, que se caracteriza por ser bilateral y progresiva. Su diagnóstico es relativamente sencillo cuando se presenta con cristales de colesterol y fosfolípidos.
Zaadia Pérez Parra, Elizabeth T Escalona Leyva, Alexeide de la C Castillo Pérez, Madelyn Jareño Ochoa, Judith Cuevas Ruiz   +4 more
doaj  

Molecular genetics and genotype-phenotype correlation of inherited corneal dystrophies [PDF]

, 2017
Corneal dystrophies are a group of inherited, primarily monogenic, disorders that compromise the transparency of the cornea and cause visual impairment. A large cohort, consisting of 191 corneal dystrophy probands, was recruited to the study with the aim
Evans, CJ
core  

Schnyder corneal dystrophy

PAMJ Clinical Medicine, 2022
Kamelia Rifai, Lalla Ouafa Cherkaoui
openaire   +1 more source

Characterization of UBIAD1 and its role in Schnyder corneal dystrophy

, 2011
Schnyder corneal dystrophy (SCD) is an inherited, autosomal dominant eye disease first described in 1924. Mutations in a novel gene, UBIAD1, were recently found to cause SCD. SCD is characterized by an abnormal deposition of cholesterol and phospholipids
Nickerson, Michael L.
core  

Pedigree of a family with Schnyder crystalline corneal dystrophy.

, 2013
Genotyped subjects are 1351, 1349, 1429, 1438, 1455, 1425, 1421, 1440, 1448, and 1437.
Duane L. Guernsey (242977), Marie-Pierre Dubé (77071), Haiyan Jiang (39944), Andrew Orr (77070), Johane Robitaille (373245), Mark E. Samuels (243000), Géraldine Asselin (373247)   +6 more
core   +1 more source