Aleman TS - Search Results

1

Quantitative Assessment of Microstructural Changes of the Retina in Infants With Congenital Zika Syndrome.

Aleman TS, Ventura CV, Cavalcanti MM, Serrano LW, Traband A, Nti AA, Gois AL, Bravo-Filho V, Martins TT, Nichols CW, Maia M, Belfort R Jr. Aleman TS, et al. JAMA Ophthalmol. 2017 Oct 1;135(10):1069-1076. doi: 10.1001/jamaophthalmol.2017.3292. JAMA Ophthalmol. 2017. PMID: 28880978 Free PMC article.

2

Macular pigment and lutein supplementation in retinitis pigmentosa and Usher syndrome.

Aleman TS, Duncan JL, Bieber ML, de Castro E, Marks DA, Gardner LM, Steinberg JD, Cideciyan AV, Maguire MG, Jacobson SG. Aleman TS, et al. Invest Ophthalmol Vis Sci. 2001 Jul;42(8):1873-81. Invest Ophthalmol Vis Sci. 2001. PMID: 11431456

3

Clinicopathologic effects of mutant GUCY2D in Leber congenital amaurosis.

Milam AH, Barakat MR, Gupta N, Rose L, Aleman TS, Pianta MJ, Cideciyan AV, Sheffield VC, Stone EM, Jacobson SG. Milam AH, et al. Among authors: aleman ts. Ophthalmology. 2003 Mar;110(3):549-58. doi: 10.1016/S0161-6420(02)01757-8. Ophthalmology. 2003. PMID: 12623820

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. Among authors: aleman ts. 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: aleman ts. 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: aleman ts. Invest Ophthalmol Vis Sci. 2006 Sep;47(9):4113-20. doi: 10.1167/iovs.06-0424. Invest Ophthalmol Vis Sci. 2006. PMID: 16936131

7

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: aleman ts. Invest Ophthalmol Vis Sci. 2006 Nov;47(11):5004-10. doi: 10.1167/iovs.06-0517. Invest Ophthalmol Vis Sci. 2006. PMID: 17065520

8

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: aleman ts. Invest Ophthalmol Vis Sci. 2007 Jan;48(1):332-8. doi: 10.1167/iovs.06-0599. Invest Ophthalmol Vis Sci. 2007. PMID: 17197551

9

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

10

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. 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.

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