Digenic Retinitis Pigmentosa Due to Mutations at the Unlinked Peripherin/ RDS and ROM1 Loci von Kajiwara, Kazuto, Berson, Eliot L., Dryja, Thaddeus P.

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Novel insights into the contributions of isocitrate dehydrogenases to the Krebs cycle from patients with retinitis pigmentosa von Hartong, D.T., Dange, M., McGee, T.L., Berson, E.L., Dryja, T.P., Colman, R.F.

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Arch Ophthalmol: clinical trial of lutein in patients with retinitis pigmentosa receiving vitamin A von Berson, E.L, Rosner, B, Sandberg, M.A

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Mutation Spectrum of the Rhodopsin Gene Among Patients with Autosomal Dominant Retinitis Pigmentosa von Dryja, Thaddeus P., Hahn, Lauri B., Cowley, Glenn S., McGee, Terri L., Berson, Eliot L.

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Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11 Allele von McGee, T.L., Devoto, M., Ott, J., Berson, E.L., Dryja, T.P.

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Further evaluation of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment: subgroup analyses von Berson, E.L, Rosner, B, Sandberg, M.A

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Further Screening of the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa von Vaithinathan, Rajani, Berson, Eliot L., Dryja, Thaddeus P.

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Hyperopia and Neovascularization in Age-related Macular Degeneration von Sandberg, Michael A., Tolentino, Michael J., Miller, Sumiko, Berson, Eliot L., Gaudio, Alexander R.

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Molecular Basis of Ornithine Aminotransferase Deficiency in B-6-Responsive and -Nonresponsive Forms of Gyrate Atrophy von Ramesh, Vijaya, McClatchey, Andrea I., Ramesh, Narayanaswamy, Benoit, Lynne A., Berson, Eliot L., Shih, Vivian E., Gusella, James F.

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Nonallelic Heterogeneity in Autosomal Dominant Retinitis Pigmentosa with Incomplete Penetrance von Kim, Stella K., Haines, Jonathan L., Betson, Eliot L., Dryja, Thaddeus P.

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