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Eye anomalies and neurological manifestations in patients with PAX6 mutations
Molecular Vision, 10/26/09
Chien YH et al. – Both novel and known PAX6 mutations were identified in the current study, and PAX6 mutations were closely associated with aniridia. Absence of a positive family history does not exclude PAX6 mutation. The frequent occurrence of developmental delay in patients with PAX6 mutation argues for a prompt diagnosis of the disease.
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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
Understanding ischemic retinopathies: emerging concepts from oxygen-induced retinopathy
Documenta Ophthalmologica, 11/03/09
Genetic cardiovascular risk factors and age-related macular degeneration
Acta Ophthalmologica, 11/02/09
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Surgical interventions for idiopathic intracranial hypertension
Current Opinion in Ophthalmology, 10/28/09
Headache and the eye
Current Opinion in Ophthalmology, 10/19/09
A retrospective study on the efficacy of total absorbed orbital doses of 12, 16 and 20 Gy combined with systemic steroid treatment in patients with Graves orbitopathy
Graefe's Archive for Clinical and Experimental Ophthalmology, 11/02/09
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