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TitleDateTypeSetname
2176Assemblage Assignment2018-12Imageuu_aah_artpr
2177Assemblage Assignment2018-12Imageuu_aah_artpr
2178Assemblage Assignment2018-12Imageuu_aah_artpr
2179Assemblage Assignment2018-12Imageuu_aah_artpr
2180Assemblage Assignment2018-12Imageuu_aah_artpr
2181Assemblage Assignment2018-12Imageuu_aah_artpr
2182Assemblage Assignment2018-12Imageuu_aah_artpr
2183Assessing for Hyperventilation-induced Nystagmus2018-01Image/MovingImageehsl_novel_gold
2184Assessment of a Fully-Automated RAPD Test as a Routine Screening Tool2018-04Image/MovingImageehsl_novel_nam
2185Assessment of a Fully-Automated RAPD Test as a Routine Screening Tool2018-04Textehsl_novel_nam
2186Assessment of Cyclotorsion Using SLO Fundus Imaging in Patients With and Without Forth Nerve Palsy2018-05Image/MovingImageehsl_novel_nam
2187Assessment of Cyclotorsion Using SLO Fundus Imaging in Patients With and Without Forth Nerve Palsy2018-05Textehsl_novel_nam
2188Assessment of Cyclotorsion Using SLO Fundus Imaging in Patients With and Without Forth Nerve Palsy2018-05Textehsl_novel_nam
2189Assessment of Neurocognitive Consequences of Call Duty in Residents Using Saccadic Eye Movements2018-03Textehsl_novel_nam
2190Association between Convergence Insufficiency and EVestG Extracted Features in Post-Concussion Syndrome2018-03Textehsl_novel_nam
2191Asynchronous Onset in Leber's Hereditary Optic Neuropathy2018-03Textehsl_novel_nam
2192Ataxia, Areflexia, and Ophthalmoplegia in a Patient with AChR Binding Antibody?2018-03Textehsl_novel_nam
2193Attendance Factors in Non-Mandatory Training in a K-6 School Setting2018-04Text; Imagewc_ir
2194Atypical cases of Leber Hereditary Optic Neuropathy2018-03Textehsl_novel_nam
2195Atypical Central Retinal Artery Occlusion As The First Manifestation Of POEMS Syndrome2018-03Textehsl_novel_nam
2196Audiometry2018-03Textehsl_novel_gold
2197Automated Evaluation of Choroidal Thickness and Minimum Rim Width Thickness in Nonarteritic Anterior Ischemic Optic Neuropathy2018-03Textehsl_novel_jno
2198Axenfeld-Rieger Syndrome with Cerebellar Dysgenesis: A Clinical Association in Patients with FOXC1 Mutation2018-03Textehsl_novel_nam
2199AZOOR and Brain White Matter Lesions2018-03Textehsl_novel_nam
2200B. Todd Troost, MD (1937-2017)2018-06Textehsl_novel_jno
2176 - 2200 of 7,536