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Molecular Vision|October 27, 1998
Autosomal dominant zonular cataract with sutural opacities is associated with a splice mutation in the betaA3/A1-crystallin geneC Kannabiran, P K Rogan, L Olmos, et al.American Journal of Ophthalmology|September 15, 1985
Comparison of the effects of Viscoat and Healon on postoperative intraocular pressureB A Barron, M Busin, C Page, et al.American Journal of Human Genetics|October 1, 1995
Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12T Padma, R Ayyagari, J S Murty, et al.Biochimica Et Biophysica Acta|March 28, 1977
Retinol receptors in corneal epithelium, stroma and endotheliumB Wiggert, D R Bergsma, R J Helmsen, et al.Journal of Ocular Pharmacology|January 1, 1987
Ganglioside administration in retinitis pigmentosaD A Newsome, F C Dorsey, J G May, et al.Investigative Ophthalmology & Visual Science|June 30, 2001
The metabolism of fatty acids in human Bietti crystalline dystrophyJ Lee, X Jiao, J F Hejtmancik, et al.Ophthalmic Paediatrics and Genetics|December 1, 1984
Cellular and humoral immune parameters among patients with retinitis pigmentosa and other retinal disordersD Benezra, I Gery, C C Chan, et al.The Journal of Clinical Investigation|February 1, 1988
An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retinaG A Mitchell, L C Brody, J Looney, et al.Investigative Ophthalmology & Visual Science|May 1, 1996
Glutathione S-transferase M1 genotype and age-related cataracts. Lack of association in an Italian populationG Alberti, M Oguni, M Podgor, et al.The Journal of Biological Chemistry|February 15, 1992
Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequencesL C Brody, G A Mitchell, C Obie, et al.Pageof 4