Gender Diversity on Corporate Boards Associated with Ophthalmology von Alexis, Dominique, Fahl, Corrinne, Higginbotham, Eve, Bateman, J. Bronwyn

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Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA) von Richter, Leslie, Flodman, Pamela, Barria von-Bischhoffshausen, Fernando, Burch, Douglas, Brown, Sandra, Nguyen, Linda, Turner, Julia, Spence, M. Anne, Bateman, J. Bronwyn

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Gene Conversion Mutation in Crystallin, β-B2 ( CRYBB2 ) in a Chilean Family with Autosomal Dominant Cataract von Bateman, J. Bronwyn, MD, von-Bischhoffshaunsen, Fernando R. Barria, MD, Richter, Leslie, MS, Flodman, Pamela, MSc, MS, Burch, Douglas, BA, Spence, M. Anne, PhD

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Novel Single-Base Deletional Mutation in Major Intrinsic Protein ( MIP) in Autosomal Dominant Cataract von Geyer, David D., Spence, M. Anne, Johannes, Meriam, Flodman, Pamela, Clancy, Kevin P., Berry, Rebecca, Sparkes, Robert S., Jonsen, Matthew D., Isenberg, Sherwin J., Bateman, J. Bronwyn

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Multiple and additive functions of ALDH3A1 and ALDH1A1: cataract phenotype and ocular oxidative damage in Aldh3a1(-/-)/Aldh1a1(-/-) knock-out mice von Lassen, Natalie, Bateman, J Bronwyn, Estey, Tia, Kuszak, Jer R, Nees, David W, Piatigorsky, Joram, Duester, Gregg, Day, Brian J, Huang, Jie, Hines, Lisa M, Vasiliou, Vasilis

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Distinct Ocular Expression in Infants and Children With Down Syndrome in Cairo, Egypt: Myopia and Heart Disease von Afifi, Hanan H, Abdel Azeem, Amira A, El-Bassyouni, Hala T, Gheith, Moataz E, Rizk, Akmal, Bateman, J. Bronwyn

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Systemic Diagnostic Testing in Patients With Apparently Isolated Uveal Coloboma von Huynh, Nancy, Blain, Delphine, Glaser, Tanya, Doss, E. Lauren, Zein, Wadih M, Lang, David M, Baker, Eva H, Hill, Suvimol, Brewer, Carmen C, Kopp, Jeffrey B, Bardakjian, Tanya M, Maumenee, Irene H, Bateman, Bronwyn J, Brooks, Brian P

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Pediatric ophthalmology bids farewell to one of its founders, Leonard Apt, MD von Isenberg, Sherwin J., MD, Demer, Joseph L., MD, PhD, Bateman, J. Bronwyn, MD

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Duane Retraction Syndrome, Nystagmus, Retinal Pigment Epitheliopathy and Epiretinal Membrane with Micro- and Pachygyria, Developmental Delay, Hearing Loss and Craniopharyngioma von D'Amelio, Savino, Lassen, Natalie, Vasiliou, Vasilis, Bateman, J. Bronwyn

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Autosomal Dominant Cataract: Intrafamilial Phenotypic Variability, Interocular Asymmetry, and Variable Progression in Four Chilean Families von Shafie, Suraiya M., Barria von-Bischhoffshausen, Fernando R., Bateman, J. Bronwyn

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A New Locus for Autosomal Dominant Cataract on Chromosome 19: Linkage Analyses and Screening of Candidate Genes von Bateman, J. Bronwyn, Richter, Leslie, Flodman, Pamela, Burch, Douglas, Brown, Sandra, Penrose, Philip, Paul, Otis, Geyer, David D, Brooks, David G, Spence, M. Anne

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Eye Disease and Care in Latin America and the Caribbean von Silva, Juan Carlos, Bateman, J.Bronwyn, Contreras, Francisco

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Multiple and Additive Functions of ALDH3A1 and ALDH1A1 von Lassen, Natalie, Bateman, J. Bronwyn, Estey, Tia, Kuszak, Jer R., Nees, David W., Piatigorsky, Joram, Duester, Gregg, Day, Brian J., Huang, Jie, Hines, Lisa M., Vasiliou, Vasilis

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Handbook of Pediatric Eye and Systemic Disease von Wright, Kenneth W, Spiegel, Peter H, Thompson, Lisa S

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Ophthalmologic Findings in Patients With Ataxia von RABIAH, PETER K., BATEMAN, J. BRONWYN, DEMER, JOSEPH L., PERLMAN, SUSAN

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Ocular Colobomata von Onwochei, Benjamin C, Simon, John W, Bateman, J.Bronwyn, Couture, Kimberly C, Mir, Envar

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Favorable Visual Outcome in Cryptococcal Meningitis von Ferreira, Rosane C., Phan, Greg, Bateman, J. Bronwyn

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Endogenous Endophthalmitis Caused by Streptococcus mitis von Harrison, Steven A., Bateman, J. Bronwyn

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The Pan American Association of Ophthalmology von Bateman, J. Bronwyn

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Optic Nerve Hypoplasia Secondary to Intracranial Teratoma von Lee, Jivianne T., Hall, Theodore R., Bateman, J. Bronwyn

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