Kolesnikova M - Search Results

1

Correlations of Full-Field Stimulus Threshold With Functional and Anatomical Outcome Measurements in Advanced Retinitis Pigmentosa.

Ngo WK, Jenny LA, Kim AH, Kolesnikova M, Greenstein VC, Tsang SH. Ngo WK, et al. Among authors: kolesnikova m. Am J Ophthalmol. 2023 Jan;245:155-163. doi: 10.1016/j.ajo.2022.07.010. Epub 2022 Jul 20. Am J Ophthalmol. 2023. PMID: 35870488 Free PMC article.

2

Clinical characteristics of high myopia in female carriers of pathogenic RPGR mutations: a case series and review of the literature.

Tran M, Kolesnikova M, Kim AH, Kowal T, Ning K, Mahajan VB, Tsang SH, Sun Y. Tran M, et al. Among authors: kolesnikova m. Ophthalmic Genet. 2023 Jun;44(3):295-303. doi: 10.1080/13816810.2022.2113544. Epub 2022 Aug 26. Ophthalmic Genet. 2023. PMID: 36017691 Free PMC article. Review.

3

Foveolar thickness as potential standardized structural outcome measurement in studies of Bietti crystalline dystrophy.

Jenny LA, Liu PK, Kolesnikova M, Duong J, Kim AH, Levi SR, Greenstein VC, Tsang SH. Jenny LA, et al. Among authors: kolesnikova m. Sci Rep. 2022 Aug 29;12(1):14706. doi: 10.1038/s41598-022-16563-y. Sci Rep. 2022. PMID: 36038562 Free PMC article.

4

Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence.

Kolesnikova M, Lima de Carvalho JR Jr, Parmann R, Kim AH, Mahajan VB, Tsang SH, Sparrow JR. Kolesnikova M, et al. Mol Genet Genomic Med. 2022 Nov;10(11):e2038. doi: 10.1002/mgg3.2038. Epub 2022 Oct 12. Mol Genet Genomic Med. 2022. PMID: 36225124 Free PMC article.

5

A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt disease.

Kolesnikova M, Oh JK, Wang J, Lee W, Zernant J, Su PY, Kim AH, Jenny LA, Yang T, Allikmets R, Tsang SH. Kolesnikova M, et al. JCI Insight. 2022 Dec 8;7(23):e162687. doi: 10.1172/jci.insight.162687. JCI Insight. 2022. PMID: 36264634 Free PMC article.

6

Effects of medications on hypoxia-inducible factor in the retina: A review.

Kim AH, Kolesnikova M, Ngo WK, Tsang SH. Kim AH, et al. Among authors: kolesnikova m. Clin Exp Ophthalmol. 2023 Apr;51(3):205-216. doi: 10.1111/ceo.14161. Epub 2023 Jan 3. Clin Exp Ophthalmol. 2023. PMID: 36594241 Review.

7

Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy.

Soucy M, Kolesnikova M, Kim AH, Tsang SH. Soucy M, et al. Among authors: kolesnikova m. Doc Ophthalmol. 2023 Jun;146(3):267-272. doi: 10.1007/s10633-022-09916-5. Epub 2023 Jan 7. Doc Ophthalmol. 2023. PMID: 36609934

8

Clinical and Therapeutic Evaluation of the Ten Most Prevalent CRB1 Mutations.

Lopes da Costa B, Kolesnikova M, Levi SR, Cabral T, Tsang SH, Maumenee IH, Quinn PMJ. Lopes da Costa B, et al. Among authors: kolesnikova m. Biomedicines. 2023 Jan 27;11(2):385. doi: 10.3390/biomedicines11020385. Biomedicines. 2023. PMID: 36830922 Free PMC article.

9

Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes.

Kolesnikova M, Lima de Carvalho JR Jr, Oh JK, Soucy M, Demirkol A, Kim AH, Tsang SH, Breazzano MP. Kolesnikova M, et al. Invest Ophthalmol Vis Sci. 2023 Mar 1;64(3):23. doi: 10.1167/iovs.64.3.23. Invest Ophthalmol Vis Sci. 2023. PMID: 36912596 Free PMC article.

10

Prime Editing Strategy to Install the PRPH2 c.828+1G>A Mutation.

Caruso SM, Tsai YT, da Costa BL, Kolesnikova M, Jenny LA, Tsang SH, Quinn PMJ. Caruso SM, et al. Among authors: kolesnikova m. Adv Exp Med Biol. 2023;1415:97-102. doi: 10.1007/978-3-031-27681-1_15. Adv Exp Med Biol. 2023. PMID: 37440020

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