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Page 1
Mitochondrial replacement in an iPSC model of Leber's hereditary optic neuropathy.
Wong RCB, Lim SY, Hung SSC, Jackson S, Khan S, Van Bergen NJ, De Smit E, Liang HH, Kearns LS, Clarke L, Mackey DA, Hewitt AW, Trounce IA, Pébay A. Wong RCB, et al. Among authors: kearns ls. Aging (Albany NY). 2017 Apr;9(4):1341-1350. doi: 10.18632/aging.101231. Aging (Albany NY). 2017. PMID: 28455970 Free PMC article.
Post-cycloplegia myopic shift in an older population.
Toh T, Kearns LS, Scotter LW, Mackey DA. Toh T, et al. Among authors: kearns ls. Ophthalmic Epidemiol. 2005 Jun;12(3):215-9. doi: 10.1080/09286580590964784. Ophthalmic Epidemiol. 2005. PMID: 16036481
PAX6 mutations may be associated with high myopia.
Hewitt AW, Kearns LS, Jamieson RV, Williamson KA, van Heyningen V, Mackey DA. Hewitt AW, et al. Among authors: kearns ls. Ophthalmic Genet. 2007 Sep;28(3):179-82. doi: 10.1080/13816810701356676. Ophthalmic Genet. 2007. PMID: 17896318
The natural history of OPA1-related autosomal dominant optic atrophy.
Cohn AC, Toomes C, Hewitt AW, Kearns LS, Inglehearn CF, Craig JE, Mackey DA. Cohn AC, et al. Among authors: kearns ls. Br J Ophthalmol. 2008 Oct;92(10):1333-6. doi: 10.1136/bjo.2007.134726. Epub 2008 Jul 24. Br J Ophthalmol. 2008. PMID: 18653586
95 results