Aleman TS - Search Results

1

Unicoronal Craniosynostosis: Is There a Lateral Difference in Retinal Morphology?

Kalmar CL, Carlson AR, Zapatero ZD, Kosyk MS, Aleman TS, Bartlett SP, Liu GT, Avery RA, Taylor JA, Swanson JW. Kalmar CL, et al. Among authors: aleman ts. J Craniofac Surg. 2021 Oct 1;32(7):2370-2372. doi: 10.1097/SCS.0000000000007810. J Craniofac Surg. 2021. PMID: 34054088

2

Noninvasive methods of detecting increased intracranial pressure.

Xu W, Gerety P, Aleman T, Swanson J, Taylor J. Xu W, et al. Childs Nerv Syst. 2016 Aug;32(8):1371-86. doi: 10.1007/s00381-016-3143-x. Epub 2016 Jun 28. Childs Nerv Syst. 2016. PMID: 27351182 Review.

3

Evaluation of Optical Coherence Tomography to Detect Elevated Intracranial Pressure in Children.

Swanson JW, Aleman TS, Xu W, Ying GS, Pan W, Liu GT, Lang SS, Heuer GG, Storm PB, Bartlett SP, Katowitz WR, Taylor JA. Swanson JW, et al. Among authors: aleman ts. JAMA Ophthalmol. 2017 Apr 1;135(4):320-328. doi: 10.1001/jamaophthalmol.2017.0025. JAMA Ophthalmol. 2017. PMID: 28241164 Free PMC article.

4

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.

5

Optical coherence tomography and visual evoked potentials in pediatric MS.

Waldman AT, Liu GT, Lavery AM, Liu G, Gaetz W, Aleman TS, Banwell BL. Waldman AT, et al. Among authors: aleman ts. Neurol Neuroimmunol Neuroinflamm. 2017 Jun 5;4(4):e356. doi: 10.1212/NXI.0000000000000356. eCollection 2017 Jul. Neurol Neuroimmunol Neuroinflamm. 2017. PMID: 28626779 Free PMC article.

6

Ocular Biomarkers of Riboflavin Transporter Deficiency.

Bulas S, Bedoukian EC, O'Neil EC, Krantz ID, Yum SW, Liu GT, Aleman TS. Bulas S, et al. Among authors: aleman ts. J Neuroophthalmol. 2023 Mar 1;43(1):110-115. doi: 10.1097/WNO.0000000000001678. Epub 2022 Aug 2. J Neuroophthalmol. 2023. PMID: 35921603

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

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

9

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. 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.

10

Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganization.

Jacobson SG, Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Windsor EA, Swider M, Herrera W, Stone EM. Jacobson SG, et al. Among authors: aleman ts. Mol Vis. 2009 Jun 2;15:1098-106. Mol Vis. 2009. PMID: 19503738 Free PMC article.

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