Schwartz SB - Search Results

1

Retinal disease expression in Bardet-Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degeneration.

Azari AA, Aleman TS, Cideciyan AV, Schwartz SB, Windsor EA, Sumaroka A, Cheung AY, Steinberg JD, Roman AJ, Stone EM, Sheffield VC, Jacobson SG. Azari AA, et al. Among authors: schwartz sb. Invest Ophthalmol Vis Sci. 2006 Nov;47(11):5004-10. doi: 10.1167/iovs.06-0517. Invest Ophthalmol Vis Sci. 2006. PMID: 17065520

2

De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosa.

Schwartz SB, Aleman TS, Cideciyan AV, Swaroop A, Jacobson SG, Stone EM. Schwartz SB, et al. Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3593-7. doi: 10.1167/iovs.03-0155. Invest Ophthalmol Vis Sci. 2003. PMID: 12882812

3

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: schwartz sb. 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

4

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. Invest Ophthalmol Vis Sci. 2005 Feb;46(2):734-43. doi: 10.1167/iovs.04-1136. Invest Ophthalmol Vis Sci. 2005. PMID: 15671307

5

ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retina.

Cideciyan AV, Swider M, Aleman TS, Sumaroka A, Schwartz SB, Roman MI, Milam AH, Bennett J, Stone EM, Jacobson SG. Cideciyan AV, et al. Among authors: schwartz sb. Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4739-46. doi: 10.1167/iovs.05-0805. Invest Ophthalmol Vis Sci. 2005. PMID: 16303974 Free PMC article.

6

Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutations.

Jacobson SG, Cideciyan AV, Sumaroka A, Aleman TS, Schwartz SB, Windsor EA, Roman AJ, Stone EM, MacDonald IM. Jacobson SG, et al. Among authors: schwartz sb. Invest Ophthalmol Vis Sci. 2006 Sep;47(9):4113-20. doi: 10.1167/iovs.06-0424. Invest Ophthalmol Vis Sci. 2006. PMID: 16936131

7

RDH12 and RPE65, visual cycle genes causing leber congenital amaurosis, differ in disease expression.

Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Schwartz SB, Windsor EA, Roman AJ, Heon E, Stone EM, Thompson DA. Jacobson SG, et al. Among authors: schwartz sb. Invest Ophthalmol Vis Sci. 2007 Jan;48(1):332-8. doi: 10.1167/iovs.06-0599. Invest Ophthalmol Vis Sci. 2007. PMID: 17197551

8

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: schwartz sb. Ophthalmology. 2007 May;114(5):895-8. doi: 10.1016/j.ophtha.2006.10.028. Epub 2007 Feb 16. Ophthalmology. 2007. PMID: 17306875

9

Macular pigment and lutein supplementation in ABCA4-associated retinal degenerations.

Aleman TS, Cideciyan AV, Windsor EA, Schwartz SB, Swider M, Chico JD, Sumaroka A, Pantelyat AY, Duncan KG, Gardner LM, Emmons JM, Steinberg JD, Stone EM, Jacobson SG. Aleman TS, et al. Among authors: schwartz sb. Invest Ophthalmol Vis Sci. 2007 Mar;48(3):1319-29. doi: 10.1167/iovs.06-0764. Invest Ophthalmol Vis Sci. 2007. PMID: 17325179 Free PMC article.

10

Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.

Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Roman AJ, Windsor EA, Steinberg JD, Branham K, Othman M, Swaroop A, Jacobson SG. Aleman TS, et al. Among authors: schwartz sb. Invest Ophthalmol Vis Sci. 2007 Oct;48(10):4759-65. doi: 10.1167/iovs.07-0453. Invest Ophthalmol Vis Sci. 2007. PMID: 17898302 Free PMC article.

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