Levin AV - Search Results

1

Genotyping microarray for CSNB-associated genes.

Zeitz C, Labs S, Lorenz B, Forster U, Uksti J, Kroes HY, De Baere E, Leroy BP, Cremers FP, Wittmer M, van Genderen MM, Sahel JA, Audo I, Poloschek CM, Mohand-Saïd S, Fleischhauer JC, Hüffmeier U, Moskova-Doumanova V, Levin AV, Hamel CP, Leifert D, Munier FL, Schorderet DF, Zrenner E, Friedburg C, Wissinger B, Kohl S, Berger W. Zeitz C, et al. Among authors: levin av. Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5919-26. doi: 10.1167/iovs.09-3548. Epub 2009 Jul 2. Invest Ophthalmol Vis Sci. 2009. PMID: 19578023 Free article.

2

Juvenile cataract-associated mutation of solute carrier SLC16A12 impairs trafficking of the protein to the plasma membrane.

Castorino JJ, Gallagher-Colombo SM, Levin AV, Fitzgerald PG, Polishook J, Kloeckener-Gruissem B, Ostertag E, Philp NJ. Castorino JJ, et al. Among authors: levin av. Invest Ophthalmol Vis Sci. 2011 Aug 29;52(9):6774-84. doi: 10.1167/iovs.10-6579. Invest Ophthalmol Vis Sci. 2011. PMID: 21778275 Free PMC article.

3

Genetics of the anterior segment dysgenesis.

Paredes DI, Capasso JE, Wyman CS, Levin AV. Paredes DI, et al. Among authors: levin av. Taiwan J Ophthalmol. 2023 Jul 18;13(4):500-504. doi: 10.4103/tjo.TJO-D-23-00062. eCollection 2023 Oct-Dec. Taiwan J Ophthalmol. 2023. PMID: 38249510 Free PMC article. Review.

4

Protein modeling and in silico analysis to assess pathogenicity of ABCA4 variants in patients with inherited retinal disease.

Cevik S, Wangtiraumnuay N, Van Schelvergem K, Tsukikawa M, Capasso J, Biswas SB, Bodt B, Levin AV, Biswas-Fiss E. Cevik S, et al. Among authors: levin av. Mol Vis. 2023 Oct 25;29:217-233. eCollection 2023. Mol Vis. 2023. PMID: 38222458 Free PMC article.

5

Retinal hemorrhage variation in inertial versus contact head injuries.

Sokoloff M, Feldman KW, Levin AV, Rockter A, Armijo-Garcia V, Musick M, Weeks K, Haney SB, Marinello M, Herman BE, Frazier TN, Carroll CL, Hymel KP; Pediatric Brain Injury Research Network (PediBIRN) Investigators. Sokoloff M, et al. Among authors: levin av. Child Abuse Negl. 2024 Mar;149:106606. doi: 10.1016/j.chiabu.2023.106606. Epub 2023 Dec 21. Child Abuse Negl. 2024. PMID: 38134727

6

Mutations in AGBL5 associated with Retinitis pigmentosa.

Paredes DI, Bello NR, Capasso JE, Procopio R, Levin AV. Paredes DI, et al. Among authors: levin av. Ophthalmic Genet. 2023 Dec 11:1-6. doi: 10.1080/13816810.2023.2291687. Online ahead of print. Ophthalmic Genet. 2023. PMID: 38078364

7

TWO CASES OF CRB1-RELATED RETINAL DYSTROPHY ASSOCIATED WITH RETINAL MASSES.

Bello NR, Pisuchpen P, de Guimarães TAC, Capasso JE, Levin AV. Bello NR, et al. Among authors: levin av. Retin Cases Brief Rep. 2023 Nov 1;17(6):714-718. doi: 10.1097/ICB.0000000000001269. Retin Cases Brief Rep. 2023. PMID: 37903307

8

Deep Learning Approach for Differentiating Etiologies of Pediatric Retinal Hemorrhages: A Multicenter Study.

Khosravi P, Huck NA, Shahraki K, Hunter SC, Danza CN, Kim SY, Forbes BJ, Dai S, Levin AV, Binenbaum G, Chang PD, Suh DW. Khosravi P, et al. Among authors: levin av. Int J Mol Sci. 2023 Oct 12;24(20):15105. doi: 10.3390/ijms242015105. Int J Mol Sci. 2023. PMID: 37894785 Free PMC article.

9

Identification and Management of a Novel PRDM5 Gene Pathologic Variant in a Family With Brittle Cornea Syndrome.

Sklar BA, Pisuchpen P, Bareket M, Milman T, Eagle RC Jr, Minor J, Procopio R, Capasso J, Levin AV, Hammersmith K. Sklar BA, et al. Among authors: levin av. Cornea. 2023 Dec 1;42(12):1572-1577. doi: 10.1097/ICO.0000000000003372. Epub 2023 Sep 15. Cornea. 2023. PMID: 37713669

10

Changes in nascent chromatin structure regulate activation of the pro-fibrotic transcriptome and myofibroblast emergence in organ fibrosis.

Basta MD, Petruk S, Summer R, Rosenbloom J, Wermuth PJ, Macarak E, Levin AV, Mazo A, Walker JL. Basta MD, et al. Among authors: levin av. iScience. 2023 Apr 6;26(5):106570. doi: 10.1016/j.isci.2023.106570. eCollection 2023 May 19. iScience. 2023. PMID: 37250334 Free PMC article.

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