Jacobson SG - Search Results

1

Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration.

Jacobson SG, Sumaroka A, Aleman TS, Cideciyan AV, Schwartz SB, Roman AJ, McInnes RR, Sheffield VC, Stone EM, Swaroop A, Wright AF. Jacobson SG, et al. Hum Mol Genet. 2004 Sep 1;13(17):1893-902. doi: 10.1093/hmg/ddh198. Epub 2004 Jun 30. Hum Mol Genet. 2004. PMID: 15229190

2

X-linked retinitis pigmentosa: functional phenotype of an RP2 genotype.

Jacobson SG, Roman AJ, Cideciyan AV, Robey MG, Iwata T, Inana G. Jacobson SG, et al. Invest Ophthalmol Vis Sci. 1992 Dec;33(13):3481-92. Invest Ophthalmol Vis Sci. 1992. PMID: 1464493

3

Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation.

Kemp CM, Jacobson SG, Roman AJ, Sung CH, Nathans J. Kemp CM, et al. Among authors: jacobson sg. Am J Ophthalmol. 1992 Feb 15;113(2):165-74. doi: 10.1016/s0002-9394(14)71529-6. Am J Ophthalmol. 1992. PMID: 1550184 Free article.

4

S cone-driven but not S cone-type electroretinograms in the enhanced S cone syndrome.

Román AJ, Jacobson SG. Román AJ, et al. Among authors: jacobson sg. Exp Eye Res. 1991 Nov;53(5):685-90. doi: 10.1016/0014-4835(91)90230-c. Exp Eye Res. 1991. PMID: 1743268 No abstract available.

5

Relatively enhanced S cone function in the Goldmann-Favre syndrome.

Jacobson SG, Román AJ, Román MI, Gass JD, Parker JA. Jacobson SG, et al. Am J Ophthalmol. 1991 Apr 15;111(4):446-53. doi: 10.1016/s0002-9394(14)72379-7. Am J Ophthalmol. 1991. PMID: 2012146 Free article.

6

Interocular asymmetry of visual function in heterozygotes of X-linked retinitis pigmentosa.

Jacobson SG, Yagasaki K, Feuer WJ, Román AJ. Jacobson SG, et al. Exp Eye Res. 1989 May;48(5):679-91. doi: 10.1016/0014-4835(89)90009-2. Exp Eye Res. 1989. PMID: 2737262 Free article.

7

Night blindness in Sorsby's fundus dystrophy reversed by vitamin A.

Jacobson SG, Cideciyan AV, Regunath G, Rodriguez FJ, Vandenburgh K, Sheffield VC, Stone EM. Jacobson SG, et al. Nat Genet. 1995 Sep;11(1):27-32. doi: 10.1038/ng0995-27. Nat Genet. 1995. PMID: 7550309

8

Enhanced S cone syndrome: evidence for an abnormally large number of S cones.

Hood DC, Cideciyan AV, Roman AJ, Jacobson SG. Hood DC, et al. Among authors: jacobson sg. Vision Res. 1995 May;35(10):1473-81. doi: 10.1016/0042-6989(95)98727-q. Vision Res. 1995. PMID: 7645276 Free article.

9

A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration.

Gorin MB, Jackson KE, Ferrell RE, Sheffield VC, Jacobson SG, Gass JD, Mitchell E, Stone EM. Gorin MB, et al. Among authors: jacobson sg. Ophthalmology. 1995 Feb;102(2):246-55. doi: 10.1016/s0161-6420(95)31029-9. Ophthalmology. 1995. PMID: 7862413 Free article.

10

Image analysis of the tapetal-like reflex in carriers of X-linked retinitis pigmentosa.

Cideciyan AV, Jacobson SG. Cideciyan AV, et al. Among authors: jacobson sg. Invest Ophthalmol Vis Sci. 1994 Oct;35(11):3812-24. Invest Ophthalmol Vis Sci. 1994. PMID: 7928178

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