Jacobson SG - Search Results

1

Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype.

Schwartz SB, Aleman TS, Cideciyan AV, Windsor EA, Sumaroka A, Roman AJ, Rane T, Smilko EE, Bennett J, Stone EM, Kimberling WJ, Liu XZ, Jacobson SG. Schwartz SB, et al. Among authors: jacobson sg. Invest Ophthalmol Vis Sci. 2005 Feb;46(2):734-43. doi: 10.1167/iovs.04-1136. Invest Ophthalmol Vis Sci. 2005. PMID: 15671307

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

Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations.

Jacobson SG, Kemp CM, Sung CH, Nathans J. Jacobson SG, et al. Am J Ophthalmol. 1991 Sep 15;112(3):256-71. doi: 10.1016/s0002-9394(14)76726-1. Am J Ophthalmol. 1991. PMID: 1882937 Free article.

6

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.

7

SWS (blue) cone hypersensitivity in a newly identified retinal degeneration.

Jacobson SG, Marmor MF, Kemp CM, Knighton RW. Jacobson SG, et al. Invest Ophthalmol Vis Sci. 1990 May;31(5):827-38. Invest Ophthalmol Vis Sci. 1990. PMID: 2335450

8

Patterns of rod and cone dysfunction in Bardet-Biedl syndrome.

Jacobson SG, Borruat FX, Apáthy PP. Jacobson SG, et al. Am J Ophthalmol. 1990 Jun 15;109(6):676-88. doi: 10.1016/s0002-9394(14)72436-5. Am J Ophthalmol. 1990. PMID: 2346197 Free article.

9

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.

10

Two types of visual dysfunction in autosomal dominant retinitis pigmentosa.

Kemp CM, Jacobson SG, Faulkner DJ. Kemp CM, et al. Among authors: jacobson sg. Invest Ophthalmol Vis Sci. 1988 Aug;29(8):1235-41. Invest Ophthalmol Vis Sci. 1988. PMID: 3417410

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