Berson, Eliot L.

Retinitis pigmentosa

Hartong, D. T., Berson, E. L., & Dryja, T. P. (2006) · The Lancet

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 2,924

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

Dryja, T. P., McGee, T. L., Reichel, E., Hahn, L. B., Cowley, G. S., Yandell, D. W., Sandberg, M. A., & Berson, E. L. (1990) · Nature

Retinal Development and DisordersGenetic and Kidney Cyst Diseases

Cited by 1,072

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis

Morimura, H., Fishman, G. A., Grover, S. A., Fulton, A. B., Berson, E. L., & Dryja, T. P. (1998) · Proceedings of the National Academy of Sciences

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 481

A Randomized Trial of Vitamin A and Vitamin E Supplementation for Retinitis Pigmentosa

Berson, E. L. (1993) · Archives of Ophthalmology

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 465

Transgenic mice with a rhodopsin mutation (Pro23His): A mouse model of autosomal dominant retinitis pigmentosa

Olsson, J. E., Gordon, J. W., Pawlyk, B. S., Roof, D., Hayes, A., Molday, R. S., Mukai, S., Cowley, G. S., Berson, E. L., & Dryja, T. P. (1992) · Neuron

Retinal Development and DisordersPhotoreceptor and optogenetics research

Cited by 455

A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

Rosenfeld, P. J., Cowley, G. S., McGee, T. L., Sandberg, M. A., Berson, E. L., & Dryja, T. P. (1992) · Nature Genetics

Retinal Development and DisordersGenetic and Kidney Cyst Diseases

Cited by 422

Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus

Yamamoto, H., Simon, A., Eriksson, U., Harris, E., Berson, E. L., & Dryja, T. P. (1999) · Nature Genetics

Retinal Development and DisordersRetinoids in leukemia and cellular processes

Cited by 298

Clinical Trial of Lutein in Patients With Retinitis Pigmentosa Receiving Vitamin A

Berson, E. L., ROSNER, B. A., Sandberg, M. A., Weigel-DiFranco, C., Brockhurst, R. J., Hayes, K. C., Johnson, E. J., Anderson, E. J., Johnson, C. A., Gaudio, A. R., et al. (2010) · Archives of Ophthalmology

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 179

Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa

Morimura, H., Saindelle-Ribeaudeau, F., Berson, E. L., & Dryja, T. P. (1999) · Nature Genetics

Retinal Development and DisordersPhotoreceptor and optogenetics research

Cited by 143

A Homozygous Missense Mutation in the IRBP Gene (RBP3) Associated with Autosomal Recessive Retinitis Pigmentosa

den Hollander, A. I., McGee, T. L., Ziviello, C., Banfi, S., Dryja, T. P., Gonzalez-Fernandez, F., Ghosh, D., & Berson, E. L. (2009) · Investigative Opthalmology & Visual Science

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 109

ω-3 Intake and Visual Acuity in Patients With Retinitis Pigmentosa Receiving Vitamin A

Berson, E. L., Rosner, B., Sandberg, M. A., Weigel-DiFranco, C., & Willett, W. C. (2012) · Archives of Ophthalmology

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 78