Aleman TS - Search Results

1

Acute Zonal Cone Photoreceptor Outer Segment Loss.

Aleman TS, Sandhu HS, Serrano LW, Traband A, Lau MK, Adamus G, Avery RA. Aleman TS, et al. JAMA Ophthalmol. 2017 May 1;135(5):487-490. doi: 10.1001/jamaophthalmol.2017.0451. JAMA Ophthalmol. 2017. PMID: 28384671 Free PMC article.

2

Retinal rod photoreceptor-specific gene mutation perturbs cone pathway development.

Banin E, Cideciyan AV, Alemán TS, Petters RM, Wong F, Milam AH, Jacobson SG. Banin E, et al. Among authors: aleman ts. Neuron. 1999 Jul;23(3):549-57. doi: 10.1016/s0896-6273(00)80807-7. Neuron. 1999. PMID: 10433266 Free article.

3

Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotype.

Aleman TS, Cideciyan AV, Volpe NJ, Stevanin G, Brice A, Jacobson SG. Aleman TS, et al. Exp Eye Res. 2002 Jun;74(6):737-45. doi: 10.1006/exer.2002.1169. Exp Eye Res. 2002. PMID: 12126946

4

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

5

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. Among authors: aleman ts. Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3593-7. doi: 10.1167/iovs.03-0155. Invest Ophthalmol Vis Sci. 2003. PMID: 12882812

6

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

7

Macular degeneration in a patient with aceruloplasminemia, a disease associated with retinal iron overload.

Dunaief JL, Richa C, Franks EP, Schultze RL, Aleman TS, Schenck JF, Zimmerman EA, Brooks DG. Dunaief JL, et al. Among authors: aleman ts. Ophthalmology. 2005 Jun;112(6):1062-5. doi: 10.1016/j.ophtha.2004.12.029. Ophthalmology. 2005. PMID: 15882908

8

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

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

Human cone photoreceptor dependence on RPE65 isomerase.

Jacobson SG, Aleman TS, Cideciyan AV, Heon E, Golczak M, Beltran WA, Sumaroka A, Schwartz SB, Roman AJ, Windsor EA, Wilson JM, Aguirre GD, Stone EM, Palczewski K. Jacobson SG, et al. Among authors: aleman ts. Proc Natl Acad Sci U S A. 2007 Sep 18;104(38):15123-8. doi: 10.1073/pnas.0706367104. Epub 2007 Sep 11. Proc Natl Acad Sci U S A. 2007. PMID: 17848510 Free PMC article.

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