Risultati della ricerca - Rebecca Sheplock

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  1. 1
    Automated Light- and Dark-Adapted Perimetry for Evaluating Retinitis Pigmentosa: Filling a Need to Accommodate Multicenter Clinical Trials

    Automated Light- and Dark-Adapted Perimetry for Evaluating Retinitis Pigmentosa: Filling a Need to Accommodate Multicenter Clinical Trials di David B. McGuigan, Alejandro J. Román, Artur V. Cideciyan, Rodrigo Matsui, Michaela Gruzensky, Rebecca Sheplock, Samuel G. Jacobson

    Pubblicazione 2016
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  2. 2
    Inner and Outer Retinal Changes in Retinal Degenerations Associated With<i>ABCA4</i>Mutations

    Inner and Outer Retinal Changes in Retinal Degenerations Associated With<i>ABCA4</i>Mutations di Wei Huang, Artur V. Cideciyan, Alejandro J. Román, Alexander Sumaroka, Rebecca Sheplock, Sharon Schwartz, Edwin M. Stone, Samuel G. Jacobson

    Pubblicazione 2014
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  3. 3
    Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiatives

    Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiatives di Alexandra V. Garafalo, Artur V. Cideciyan, Elise Héon, Rebecca Sheplock, Alexander Pearson, Caberry W. Yu, Alexander Sumaroka, Gustavo D. Aguirre, Samuel G. Jacobson

    Pubblicazione 2019
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  4. 4
    <i>TULP1</i>Mutations Causing Early-Onset Retinal Degeneration: Preserved but Insensitive Macular Cones

    <i>TULP1</i>Mutations Causing Early-Onset Retinal Degeneration: Preserved but Insensitive Macular Cones di Samuel G. Jacobson, Artur V. Cideciyan, Wei Huang, Alexander Sumaroka, Alejandro J. Román, Sharon Schwartz, Xunda Luo, Rebecca Sheplock, Joanna M. Dauber, Małgorzata Świder, Edwin M. Stone

    Pubblicazione 2014
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  5. 5
    Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the <i>CEP290</i> Gene

    Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the <i>CEP290</i> Gene di Samuel G. Jacobson, Artur V. Cideciyan, Alexander Sumaroka, Alejandro J. Román, Jason Charng, Monica Lu, Windy Choi, Rebecca Sheplock, Małgorzata Świder, Mychajlo S. Kosyk, Sharon Schwartz, Edwin M. Stone, Gerald A. Fishman

    Pubblicazione 2017
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  6. 6
    Safety and improved efficacy signals following gene therapy in childhood blindness caused by GUCY2D mutations

    Safety and improved efficacy signals following gene therapy in childhood blindness caused by GUCY2D mutations di Samuel G. Jacobson, Artur V. Cideciyan, Allen C. Ho, Igor V. Peshenko, Alexandra V. Garafalo, Alejandro J. Román, Alexander Sumaroka, Vivian Wu, Arun K. Krishnan, Rebecca Sheplock, Sanford L. Boye, Bee-Lin Cheang, Vanessa Davidson, Catherine R. O’Riordan, Alexander M. Dizhoor, Sanford L. Boye

    Pubblicazione 2021
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