検索結果 - Alexandra V. Garafalo

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  1. 1
    Full-field stimulus testing: Role in the clinic and as an outcome measure in clinical trials of severe childhood retinal disease

    Full-field stimulus testing: Role in the clinic and as an outcome measure in clinical trials of severe childhood retinal disease 著者: Alejandro J. Román, Artur V. Cideciyan, Vivian Wu, Alexandra V. Garafalo, Samuel G. Jacobson

    出版事項 2021
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  2. 2
    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 著者: Alexandra V. Garafalo, Artur V. Cideciyan, Elise Héon, Rebecca Sheplock, Alexander Pearson, Caberry W. Yu, Alexander Sumaroka, Gustavo D. Aguirre, Samuel G. Jacobson

    出版事項 2019
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  3. 3
    Durable vision improvement after a single treatment with antisense oligonucleotide sepofarsen: a case report

    Durable vision improvement after a single treatment with antisense oligonucleotide sepofarsen: a case report 著者: Artur V. Cideciyan, Samuel G. Jacobson, Allen C. Ho, Alexandra V. Garafalo, Alejandro J. Román, Alexander Sumaroka, Arun K. Krishnan, Małgorzata Świder, Michael R. Schwartz, Aniz Girach

    出版事項 2021
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  4. 4
    EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression

    EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression 著者: David B. McGuigan, Elise Héon, Artur V. Cideciyan, Rinki Ratnapriya, Monica Lu, Alexander Sumaroka, Alejandro J. Román, Vaishnavi Batmanabane, Alexandra V. Garafalo, Edwin M. Stone, Anand Swaroop, Samuel G. Jacobson

    出版事項 2017
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  5. 5
    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 著者: 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

    出版事項 2021
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    Artigo
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  6. 6
    Night vision restored in days after decades of congenital blindness

    Night vision restored in days after decades of congenital blindness 著者: Samuel G. Jacobson, Artur V. Cideciyan, Allen C. Ho, Alejandro J. Román, Vivian Wu, Alexandra V. Garafalo, Alexander Sumaroka, Arun K. Krishnan, Małgorzata Świder, Abraham A. Mascio, Christine N. Kay, Dan Yoon, Kenji P. Fujita, Sanford L. Boye, Igor V. Peshenko, Alexander M. Dizhoor, Sanford L. Boye

    出版事項 2022
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    Artigo
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  7. 7
    Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10: a phase 1b/2 trial

    Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10: a phase 1b/2 trial 著者: Stephen R. Russell, Arlene V. Drack, Artur V. Cideciyan, Samuel G. Jacobson, Bart P. Leroy, Caroline Van Cauwenbergh, Allen C. Ho, Alina V. Dumitrescu, Ian C. Han, M. Carmen Marcos Martin, Wanda Pfeifer, Elliott H. Sohn, Jean Walshire, Alexandra V. Garafalo, Arun K. Krishnan, Christian A. Powers, Alexander Sumaroka, Alejandro J. Román, Eva Vanhonsebrouck, Eltanara A. Jones, Fanny Nerinckx, Julie De Zaeytijd, Rob W.J. Collin, Carel B. Hoyng, Peter Adamson, Michael E. Cheetham, Michael R. Schwartz, Wilhelmina den Hollander, Friedrich Asmus, Gerard Platenburg, David M. Rodman, Aniz Girach

    出版事項 2022
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    Artigo
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