Roman AJ - Search Results

1

Leber congenital amaurosis caused by an RPGRIP1 mutation shows treatment potential.

Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Schwartz SB, Roman AJ, Stone EM. Jacobson SG, et al. Among authors: roman aj. Ophthalmology. 2007 May;114(5):895-8. doi: 10.1016/j.ophtha.2006.10.028. Epub 2007 Feb 16. Ophthalmology. 2007. PMID: 17306875

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. Among authors: roman aj. 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: roman aj. 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. 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. Among authors: roman mi, roman aj. 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. Among authors: roman aj. 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

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: roman aj. Vision Res. 1995 May;35(10):1473-81. doi: 10.1016/0042-6989(95)98727-q. Vision Res. 1995. PMID: 7645276 Free article.

8

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. Among authors: roman aj. 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

9

Lifespan and mitochondrial control of neurodegeneration.

Wright AF, Jacobson SG, Cideciyan AV, Roman AJ, Shu X, Vlachantoni D, McInnes RR, Riemersma RA. Wright AF, et al. Among authors: roman aj. Nat Genet. 2004 Nov;36(11):1153-8. doi: 10.1038/ng1448. Nat Genet. 2004. PMID: 15514669 Review.

10

Quantifying rod photoreceptor-mediated vision in retinal degenerations: dark-adapted thresholds as outcome measures.

Roman AJ, Schwartz SB, Aleman TS, Cideciyan AV, Chico JD, Windsor EA, Gardner LM, Ying GS, Smilko EE, Maguire MG, Jacobson SG. Roman AJ, et al. Exp Eye Res. 2005 Feb;80(2):259-72. doi: 10.1016/j.exer.2004.09.008. Exp Eye Res. 2005. PMID: 15670804

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