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Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy.
Khan KN, El-Asrag ME, Ku CA, Holder GE, McKibbin M, Arno G, Poulter JA, Carss K, Bommireddy T, Bagheri S, Bakall B, Scholl HP, Raymond FL, Toomes C, Inglehearn CF, Pennesi ME, Moore AT, Michaelides M, Webster AR, Ali M; for NIHR BioResource-Rare Diseases and UK Inherited Retinal Disease Consortium. Khan KN, et al. Among authors: pennesi me. Invest Ophthalmol Vis Sci. 2017 Jun 1;58(7):2906-2914. doi: 10.1167/iovs.16-20608. Invest Ophthalmol Vis Sci. 2017. PMID: 28586915 Free article.
Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium.
Thompson DA, Ali RR, Banin E, Branham KE, Flannery JG, Gamm DM, Hauswirth WW, Heckenlively JR, Iannaccone A, Jayasundera KT, Khan NW, Molday RS, Pennesi ME, Reh TA, Weleber RG, Zacks DN; Monaciano Consortium. Thompson DA, et al. Among authors: pennesi me. Invest Ophthalmol Vis Sci. 2015 Feb 9;56(2):918-31. doi: 10.1167/iovs.14-16049. Invest Ophthalmol Vis Sci. 2015. PMID: 25667399 Free PMC article. Review.
Retinal Gene Therapy: Current Progress and Future Prospects.
Ku CA, Pennesi ME. Ku CA, et al. Among authors: pennesi me. Expert Rev Ophthalmol. 2015 Jun;10(3):281-299. doi: 10.1586/17469899.2015.1035711. Epub 2015 Apr 10. Expert Rev Ophthalmol. 2015. PMID: 26609316 Free PMC article.
Gene Therapy Trial Update: A Primer for Vitreoretinal Specialists.
Ku CA, Hariprasad SM, Pennesi ME. Ku CA, et al. Among authors: pennesi me. Ophthalmic Surg Lasers Imaging Retina. 2016 Jan;47(1):6-12. doi: 10.3928/23258160-20151214-01. Ophthalmic Surg Lasers Imaging Retina. 2016. PMID: 26731203 No abstract available.
186 results