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Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome.
Igelman AD, Ku C, da Palma MM, Georgiou M, Schiff ER, Lam BL, Sankila EM, Ahn J, Pyers L, Vincent A, Ferraz Sallum JM, Zein WM, Oh JK, Maldonado RS, Ryu J, Tsang SH, Gorin MB, Webster AR, Michaelides M, Yang P, Pennesi ME. Igelman AD, et al. Ophthalmic Genet. 2021 Dec;42(6):664-673. doi: 10.1080/13816810.2021.1946704. Epub 2021 Jul 5. Ophthalmic Genet. 2021. PMID: 34223797 Free PMC article.
The new landscape of retinal gene therapy.
Ku CA, Pennesi ME. Ku CA, et al. Am J Med Genet C Semin Med Genet. 2020 Sep;184(3):846-859. doi: 10.1002/ajmg.c.31842. Epub 2020 Sep 5. Am J Med Genet C Semin Med Genet. 2020. PMID: 32888388 Review.
Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome.
da Palma MM, Igelman AD, Ku C, Burr A, You JY, Place EM, Wang NK, Oh JK, Branham KE, Zhang X, Ahn J, Gorin MB, Lam BL, Ronquillo CC, Bernstein PS, Nagiel A, Huckfeldt R, Cabrera MT, Kelly JP, Bakall B, Iannaccone A, Hufnagel RB, Zein WM, Koenekoop RK, Birch DG, Yang P, Fahim AT, Pennesi ME. da Palma MM, et al. Invest Ophthalmol Vis Sci. 2021 Jun 1;62(7):27. doi: 10.1167/iovs.62.7.27. Invest Ophthalmol Vis Sci. 2021. PMID: 34185059 Free PMC article.
Vitelliform maculopathy in MELAS syndrome.
Jahrig C, Ku CA, Marra M, Pennesi ME, Yang P. Jahrig C, et al. Among authors: ku ca. Am J Ophthalmol Case Rep. 2023 Apr 6;30:101842. doi: 10.1016/j.ajoc.2023.101842. eCollection 2023 Jun. Am J Ophthalmol Case Rep. 2023. PMID: 37096132 Free PMC article.
33 results