Levi SR - Search Results

1

Precision Medicine Trials in Retinal Degenerations.

Levi SR, Ryu J, Liu PK, Tsang SH. Levi SR, et al. Annu Rev Vis Sci. 2021 Sep 15;7:851-865. doi: 10.1146/annurev-vision-100419-111701. Annu Rev Vis Sci. 2021. PMID: 34524878 Review.

2

Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa.

Oh JK, Lima de Carvalho JR Jr, Sun YJ, Ragi S, Yang J, Levi SR, Ryu J, Bassuk AG, Mahajan VB, Tsang SH. Oh JK, et al. Among authors: levi sr. Orphanet J Rare Dis. 2019 Dec 19;14(1):295. doi: 10.1186/s13023-019-1275-2. Orphanet J Rare Dis. 2019. PMID: 31856884 Free PMC article.

3

Fundoscopy-directed genetic testing to re-evaluate negative whole exome sequencing results.

Cho A, Lima de Carvalho JR Jr, Tanaka AJ, Jauregui R, Levi SR, Bassuk AG, Mahajan VB, Tsang SH. Cho A, et al. Among authors: levi sr. Orphanet J Rare Dis. 2020 Jan 30;15(1):32. doi: 10.1186/s13023-020-1312-1. Orphanet J Rare Dis. 2020. PMID: 32000842 Free PMC article.

4

Progressive RPE atrophy and photoreceptor death in KIZ-associated autosomal recessive retinitis pigmentosa.

Lin Y, Xu CL, Breazzano MP, Tanaka AJ, Ryu J, Levi SR, Yao K, Sparrow JR, Tsang SH. Lin Y, et al. Among authors: levi sr. Ophthalmic Genet. 2020 Feb;41(1):26-30. doi: 10.1080/13816810.2020.1723116. Epub 2020 Feb 13. Ophthalmic Genet. 2020. PMID: 32052671 Free PMC article.

5

Comparative Analysis of Functional and Structural Decline in Retinitis Pigmentosas.

Cabral T, Lima de Carvalho JR Jr, Kim J, Oh JK, Levi SR, Park KS, Duong JK, Park J, Boudreault K, Belfort R Jr, Tsang SH. Cabral T, et al. Among authors: levi sr. Int J Mol Sci. 2020 Apr 15;21(8):2730. doi: 10.3390/ijms21082730. Int J Mol Sci. 2020. PMID: 32326409 Free PMC article.

6

PKM2 ablation enhanced retinal function and survival in a preclinical model of retinitis pigmentosa.

Zhang E, Ryu J, Levi SR, Oh JK, Hsu CW, Cui X, Lee TT, Wang NK, Lima de Carvalho JR, Tsang SH. Zhang E, et al. Among authors: levi sr. Mamm Genome. 2020 Apr;31(3-4):77-85. doi: 10.1007/s00335-020-09837-1. Epub 2020 Apr 27. Mamm Genome. 2020. PMID: 32342224 Free PMC article.

7

Differences in Intraretinal Pigment Migration Across Inherited Retinal Dystrophies.

Oh JK, Levi SR, Kim J, Lima de Carvalho JR Jr, Ryu J, Sparrow JR, Tsang SH. Oh JK, et al. Among authors: levi sr. Am J Ophthalmol. 2020 Sep;217:252-260. doi: 10.1016/j.ajo.2020.05.010. Epub 2020 May 20. Am J Ophthalmol. 2020. PMID: 32442431 Free PMC article.

8

Optical Gap Biomarker in Cone-Dominant Retinal Dystrophy.

Oh JK, Ryu J, Lima de Carvalho JR Jr, Levi SR, Lee W, Tsamis E, Greenstein VC, Mahajan VB, Allikmets R, Tsang SH. Oh JK, et al. Among authors: levi sr. Am J Ophthalmol. 2020 Oct;218:40-53. doi: 10.1016/j.ajo.2020.05.016. Epub 2020 May 21. Am J Ophthalmol. 2020. PMID: 32445700 Free PMC article.

9

Quantitative Autofluorescence Following Gene Therapy With Voretigene Neparvovec.

Levi SR, Oh JK, de Carvalho JRL Jr, Mahajan VB, Tsang SH, Sparrow JR. Levi SR, et al. JAMA Ophthalmol. 2020 Aug 1;138(8):919-921. doi: 10.1001/jamaophthalmol.2020.2018. JAMA Ophthalmol. 2020. PMID: 32556084 Free PMC article. No abstract available.

10

Commentary on "Exome sequencing and electro-clinical features in pediatric patients with very early-onset retinal dystrophies: A cohort study".

Heydari K, Levi SR, Tsang SH. Heydari K, et al. Among authors: levi sr. Eur J Paediatr Neurol. 2021 Mar;31:106-107. doi: 10.1016/j.ejpn.2021.03.004. Epub 2021 Mar 8. Eur J Paediatr Neurol. 2021. PMID: 33736886 No abstract available.

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