CRISTY KU to Humans
This is a "connection" page, showing publications CRISTY KU has written about Humans.
Connection Strength
0.187
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Perimacular Atrophy Following Voretigene Neparvovec-Rzyl Treatment in the Setting of Previous Contralateral Eye Treatment With a Different Viral Vector. Transl Vis Sci Technol. 2024 Jun 03; 13(6):11.
Score: 0.025
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Improved Rod Sensitivity as Assessed by Two-Color Dark-Adapted Perimetry in Patients With RPE65-Related Retinopathy Treated With Voretigene Neparvovec-rzyl. Transl Vis Sci Technol. 2023 04 03; 12(4):17.
Score: 0.023
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Stargardt Disease: Gene Therapy Strategies for ABCA4. Int Ophthalmol Clin. 2021 10 01; 61(4):157-165.
Score: 0.021
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The new landscape of retinal gene therapy. Am J Med Genet C Semin Med Genet. 2020 09; 184(3):846-859.
Score: 0.019
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Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration. JAMA Ophthalmol. 2017 07 01; 135(7):749-760.
Score: 0.015
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Spectrum of ocular manifestations in cobalamin C and cobalamin A types of methylmalonic acidemia. Ophthalmic Genet. 2016 12; 37(4):404-414.
Score: 0.014
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Gene Therapy Trial Update: A Primer for Vitreoretinal Specialists. Ophthalmic Surg Lasers Imaging Retina. 2016 Jan; 47(1):6-12.
Score: 0.014
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Viral-mediated vision rescue of a novel AIPL1 cone-rod dystrophy model. Hum Mol Genet. 2015 Feb 01; 24(3):670-84.
Score: 0.013
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Expanding the phenotypic and genotypic spectrum of patients with HGSNAT-related retinopathy. Ophthalmic Genet. 2024 Apr; 45(2):167-174.
Score: 0.006
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A possible ocular biomarker for response to hyperornithinemia in gyrate atrophy: the effect of pyridoxine, lysine, and arginine-restricted diet in a patient with advanced disease. Ophthalmic Genet. 2023 04; 44(2):191-197.
Score: 0.005
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Three-Year Safety Results of SAR422459 (EIAV-ABCA4) Gene Therapy in Patients With ABCA4-Associated Stargardt Disease: An Open-Label Dose-Escalation Phase I/IIa Clinical Trial, Cohorts 1-5. Am J Ophthalmol. 2022 08; 240:285-301.
Score: 0.005
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Inherited Retinal Disease Panels-Caveat Emptor-Truly Know Your Inherited Retinal Disease Panel. Retina. 2022 01 01; 42(1):1-3.
Score: 0.005
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Effect of Pharmacological Pupil Dilation on Dark-Adapted Perimetric Sensitivity in Healthy Subjects Using an Octopus 900 Perimeter. Transl Vis Sci Technol. 2021 12 01; 10(14):18.
Score: 0.005
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Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome. Ophthalmic Genet. 2021 12; 42(6):664-673.
Score: 0.005
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Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome. Invest Ophthalmol Vis Sci. 2021 06 01; 62(7):27.
Score: 0.005
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Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy. Invest Ophthalmol Vis Sci. 2017 06 01; 58(7):2906-2914.
Score: 0.004
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Molecular and Clinical Findings in Patients With Knobloch Syndrome. JAMA Ophthalmol. 2016 07 01; 134(7):753-62.
Score: 0.004