Aleman TS - Search Results

1

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

2

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.

3

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.

4

Detailed retinal phenotype of Boucher-Neuhäuser syndrome associated with mutations in PNPLA6 mimicking choroideremia.

O'Neil E, Serrano L, Scoles D, Cunningham KE, Han G, Chiang J, Bennett J, Aleman TS. O'Neil E, et al. Among authors: aleman ts. Ophthalmic Genet. 2019 Jun;40(3):267-275. doi: 10.1080/13816810.2019.1605392. Epub 2019 May 28. Ophthalmic Genet. 2019. PMID: 31135245

5

ENHANCED S-CONE SYNDROME: VISUAL FUNCTION, CROSS-SECTIONAL IMAGING, AND CELLULAR STRUCTURE WITH ADAPTIVE OPTICS OPHTHALMOSCOPY.

Ammar MJ, Scavelli KT, Uyhazi KE, Bedoukian EC, Serrano LW, Edelstein ID, Vergilio G, Cooper RF, Morgan JIW, Kumar P, Aleman TS. Ammar MJ, et al. Among authors: aleman ts. Retin Cases Brief Rep. 2021 Nov 1;15(6):694-701. doi: 10.1097/ICB.0000000000000891. Retin Cases Brief Rep. 2021. PMID: 31306293 Free PMC article.

6

NMNAT1-ASSOCIATED CONE-ROD DYSTROPHY: EVIDENCE FOR A SPECTRUM OF FOVEAL MALDEVELOPMENT.

Bedoukian EC, Zhu X, Serrano LW, Scoles D, Aleman TS. Bedoukian EC, et al. Among authors: aleman ts. Retin Cases Brief Rep. 2022 May 1;16(3):385-392. doi: 10.1097/ICB.0000000000000992. Epub 2020 Mar 4. Retin Cases Brief Rep. 2022. PMID: 32150116

7

A Virtual Reality Orientation and Mobility Test for Inherited Retinal Degenerations: Testing a Proof-of-Concept After Gene Therapy.

Aleman TS, Miller AJ, Maguire KH, Aleman EM, Serrano LW, O'Connor KB, Bedoukian EC, Leroy BP, Maguire AM, Bennett J. Aleman TS, et al. Among authors: aleman em. Clin Ophthalmol. 2021 Mar 2;15:939-952. doi: 10.2147/OPTH.S292527. eCollection 2021. Clin Ophthalmol. 2021. PMID: 33688162 Free PMC article.

8

Bardet-Biedl syndrome-7 (BBS7) shows treatment potential and a cone-rod dystrophy phenotype that recapitulates the non-human primate model.

Aleman TS, O'Neil EC, O'Connor K, Jiang YY, Aleman IA, Bennett J, Morgan JIW, Toussaint BW. Aleman TS, et al. Among authors: aleman ia. Ophthalmic Genet. 2021 Jun;42(3):252-265. doi: 10.1080/13816810.2021.1888132. Epub 2021 Mar 17. Ophthalmic Genet. 2021. PMID: 33729075 Free PMC article.

9

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

10

Compound Heterozygous Mutations in ZNF408 in a Patient with a Late Onset Pigmentary Retinopathy and Relatively Preserved Central Retina.

Nadelmann JB, O'Neil EC, Kim DS, Juusola J, Aleman TS. Nadelmann JB, et al. Among authors: aleman ts. Doc Ophthalmol. 2021 Dec;143(3):305-312. doi: 10.1007/s10633-021-09847-7. Epub 2021 Jul 14. Doc Ophthalmol. 2021. PMID: 34259982

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