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Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in Southern India
Molecular Vision, 09/09/09
Sundaresan P et al. – These data suggest that LCA in India is caused primarily by a different set of mutations in the same genes associated with disease in northern America, or by mutations in other genes that have not yet been discovered.
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MTHFR gene C677T and A1298C polymorphisms and homocysteine levels in primary open angle and primary closed angle glaucoma
Molecular Vision, 11/09/09
IL-33 shifts macrophage polarization, promoting resistance against Pseudomonas aeruginosa keratitis
Investigative Ophthalmology and Visual Science, 11/23/09
Understanding ischemic retinopathies: emerging concepts from oxygen-induced retinopathy
Documenta Ophthalmologica, 11/03/09
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Vitamin C supplements and the risk of age-related cataract: a population-based prospective cohort study in women
American Journal of Clinical Nutrition, 11/20/09
Incidence and Factors Related to Macular Hole Reopening
American Journal of Ophthalmology, 10/29/09
Comparison of the AcrySof SA60 spherical intraocular lens and the AcrySof Toric SN60T3 intraocular lens outcomes in patients with low amounts of corneal astigmatism
Clinical and Experimental Ophthalmology, 11/03/09
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