Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosa von Pawlyk, B S, Bulgakov, O V, Sun, X, Adamian, M, Shu, X, Smith, A J, Berson, E L, Ali, R R, Khani, S, Wright, A F, Sandberg, M A, Li, T

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The Association between Visual Acuity and Central Retinal Thickness in Retinitis Pigmentosa von Sandberg, Michael A, Brockhurst, Robert J, Gaudio, Alexander R, Berson, Eliot L

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Night Blindness and Abnormal Cone Electroretinogram ON Responses in Patients with Mutations in the GRM6 Gene Encoding mGluR6 von Dryja, Thaddeus P., McGee, Terri L., Berson, Eliot L., Fishman, Gerald A., Sandberg, Michael A., Alexander, Kenneth R., Derlacki, Deborah J., Rajagopalan, Aruna S.

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Replacement Gene Therapy with a Human RPGRIP1 Sequence Slows Photoreceptor Degeneration in a Murine Model of Leber Congenital Amaurosis von PAWLYK, Basil S, BULGAKOV, Oleg V, XIAOQING LIU, XIAOYUN XU, ADAMIAN, Michael, XUN SUN, KHANI, Shahrokh C, BERSON, Eliot L, SANDBERG, Michael A, TIANSEN LI

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RP2 and RPGR Mutations and Clinical Correlations in Patients with X-Linked Retinitis Pigmentosa von Sharon, Dror, Sandberg, Michael A., Rabe, Vivian W., Stillberger, Melissa, Dryja, Thaddeus P., Berson, Eliot L.

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Mutations in the RPE65 Gene in Patients with Autosomal Recessive Retinitis Pigmentosa or Leber Congenital Amaurosis von Morimura, Hiroyuki, Fishman, Gerald A., Grover, Sandeep A., Fulton, Anne B., Berson, Eliot L., Dryja, Thaddeus P.

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Mutations in the gene encoding 11- cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus von Dryja, Thaddeus P, Yamamoto, Hiroyuki, Simon, András, Eriksson, Ulf, Harris, Eddie, Berson, Eliot L

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Retinitis pigmentosa : the Friedenwald lecture von BERSON, E. L

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Null RPGRIP1 Alleles in Patients with Leber Congenital Amaurosis von Dryja, Thaddeus P., Adams, Scott M., Grimsby, Jonna L., McGee, Terri L., Hong, Dong-Hyun, Li, Tiansen, Andréasson, Sten, Berson, Eliot L.

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Missense Mutation in the USH2A Gene: Association with Recessive Retinitis Pigmentosa without Hearing Loss von Rivolta, Carlo, Sweklo, Elizabeth A., Berson, Eliot L., Dryja, Thaddeus P.

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Cone cGMP‐gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases von Nishiguchi, Koji M., Sandberg, Michael A., Gorji, Nasim, Berson, Eliot L., Dryja, Thaddeus P.

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Disease Progression in Patients with Dominant Retinitis Pigmentosa and Rhodopsin Mutations von Berson, Eliot L, Rosner, Bernard, Weigel-DiFranco, Carol, Dryja, Thaddeus P, Sandberg, Michael A

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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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A Retinitis Pigmentosa GTPase Regulator (RPGR)-Deficient Mouse Model for X-Linked Retinitis Pigmentosa (RP3) von Hong, Dong-Hyun, Pawlyk, Basil S., Shang, Jingzi, Sandberg, Michael A., Berson, Eliot L., Li, Tiansen

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Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa von Seyedahmadi, Babak Jian, Rivolta, Carlo, Keene, Julia A., Berson, Eliot L., Dryja, Thaddeus P.

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Recessive NRL Mutations in Patients with Clumped Pigmentary Retinal Degeneration and Relative Preservation of Blue Cone Function von Nishiguchi, Koji M., Friedman, James S., Sandberg, Michael A., Swaroop, Anand, Berson, Eliot L., Dryja, Thaddeus P.

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Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation von Dryja, Thaddeus P, Nishiguchi, Koji M, Sandberg, Michael A, Kooijman, Aart C, Martemyanov, Kirill A, Pott, Jan W. R, Hagstrom, Stephanie A, Arshavsky, Vadim Y, Berson, Eliot L

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Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness von Yamamoto, Shuji, Sippel, Kimberly C, Berson, Eliot L, Dryja, Thaddeus P

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Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa von Pierce, Eric A, Quinn, Tracey, Meehan, Terrence, McGee, Terri L, Berson, Eliot L, Dryja, Thaddeus P

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Recessive mutations in the CYP4V2 gene in East Asian and Middle Eastern patients with Bietti crystalline corneoretinal dystrophy von Lin, J, Nishiguchi, K M, Nakamura, M, Dryja, T P, Berson, E L, Miyake, Y

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