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See Latest ArticlesExpanding the Phenotype of a Neurofibromatosis Type 1-Like Syndrome: A Patient With a SPRED1 Mutation and Orbital Manifestations
Ophthalmic Plastic and Reconstructive Surgery, 10/02/09
Lane KA et al. – A 4–year–old child with no medical history presented for evaluation of a small, palpable nodule near the left inferolateral rim. The lesion had a bluish hue and had been slowly enlarging over the course of several months. MRI of the orbits revealed a heterogenous and infiltrative preseptal and extraconal mass which enhanced with gadolinium, and sphenoid wing dysplasia on the left.
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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
Today in Pediatric Ophthalmology...keeping you current
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Ocular manifestations of the Johanson-Blizzard syndrome
Journal of American Association for Pediatric Ophthalmology and Strabismus , 11/03/09
Retinopathy of Prematurity
NeoReviews, 11/04/09
Trilateral retinoblastoma: Potentially curable with intensive chemotherapy
Pediatric Blood & Cancer, 11/16/09
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