نتائج البحث - Suzanne Yzer

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  1. 1
    Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype

    Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype حسب Stephen H. Tsang, Tomas R. Burke, Maris Oll, Suzanne Yzer, Winston Lee, Ya‐Jing Xie, Rando Allikmets

    منشور في 2014
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    Artigo
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  2. 2
    Reticular Pseudodrusen in Early Age-Related Macular Degeneration Are Associated With Choroidal Thinning

    Reticular Pseudodrusen in Early Age-Related Macular Degeneration Are Associated With Choroidal Thinning حسب Aakriti Garg Shukla, Maris Oll, Suzanne Yzer, Stanley Chang, Gaetano R. Barile, John C. Merriam, Stephen H. Tsang, Srilaxmi Bearelly

    منشور في 2013
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  3. 3
    Expanded Clinical Spectrum of Enhanced S-Cone Syndrome

    Expanded Clinical Spectrum of Enhanced S-Cone Syndrome حسب Suzanne Yzer, Irene Barbazetto, Rando Allikmets, Mary J. van Schooneveld, Arthur A. Bergen, Stephen H. Tsang, Samuel G. Jacobson, Lawrence A. Yannuzzi

    منشور في 2013
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  4. 4
    Clinical characteristics and long-term visual outcome of severe phenotypes of chronic central serous chorioretinopathy

    Clinical characteristics and long-term visual outcome of severe phenotypes of chronic central serous chorioretinopathy حسب Danial Mohabati, Thomas J. van Rijssen, Elon Van Dijk, Gregorius P. M. Luyten, Tom Missotten, Carel C B Hoyng, Suzanne Yzer, Camiel J. F. Boon

    منشور في 2018
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    Artigo
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  5. 5
    Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone–rod dystrophy and retinitis pigmentosa

    Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone–rod dystrophy and retinitis pigmentosa حسب B. Jeroen Klevering, Suzanne Yzer, Klaus Rohrschneider, Marijke N. Zonneveld, Rando Allikmets, L. Ingeborgh van den Born, Alessandra Maugeri, Carel B. Hoyng, Frans P.M. Cremers

    منشور في 2004
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    Artigo
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  6. 6
    Discrepancy in current central serous chorioretinopathy classification

    Discrepancy in current central serous chorioretinopathy classification حسب Sumit Randhir Singh, Alexandre Matet, Elon H. C. van Dijk, Alejandra Daruich, Sascha Fauser, Suzanne Yzer, Enrico Peiretti, Sobha Sivaprasad, Andrew Lotery, Camiel J. F. Boon, Francine Béhar‐Cohen, K. Bailey Freund, Jay Chhablani

    منشور في 2018
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  7. 7
    Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

    Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis حسب Anneke I. den Hollander, Robert K. Koenekoop, Suzanne Yzer, Irma López, Maarten Arends, Krysta Voesenek, Marijke N. Zonneveld, Tim M. Strom, Thomas Meitinger, Han G. Brunner, Carel B. Hoyng, L. Ingeborgh van den Born, Klaus Rohrschneider, Frans P.M. Cremers

    منشور في 2006
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    Artigo
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  8. 8
    Cadherin 5 is Regulated by Corticosteroids and Associated with Central Serous Chorioretinopathy

    Cadherin 5 is Regulated by Corticosteroids and Associated with Central Serous Chorioretinopathy حسب Carl Schubert, Anders Pryds, Shemin Zeng, Ya‐Jing Xie, K. Bailey Freund, Richard F. Spaide, John C. Merriam, Irene Barbazetto, Jason S. Slakter, Stanley Chang, Inger Christine Munch, Arlene V. Drack, Jasmine Hernández, Suzanne Yzer, Joanna E. Merriam, Allan Linneberg, Michael Larsen, Lawrence A. Yannuzzi, Robert F. Mullins, Rando Allikmets

    منشور في 2014
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    Artigo
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  9. 9
    Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants

    Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants حسب Hedwig M. Velde, Janine Reurink, Sebastian Held, Catherina H. Z. Li, Suzanne Yzer, Jaap Oostrik, Jack Weeda, Lonneke Haer‐Wigman, Helger G. Yntema, Susanne Roosing, Laurenz Pauleikhoff, Clemens Lange, Laura Whelan, Adrian Dockery, Julia Zhu, David Keegan, G. Jane Farrar, Hannie Kremer, Cris Lanting, Markus Daμμe, Ronald J. E. Pennings

    منشور في 2022
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    Artigo
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  10. 10
    Retinal degeneration associated with RDH12 mutations results from decreased 11- cis retinal synthesis due to disruption of the visual cycle

    Retinal degeneration associated with RDH12 mutations results from decreased 11- cis retinal synthesis due to disruption of the visual cycle حسب Debra A. Thompson, Andreas Janecke, Jessica Lange, Kecia L. Feathers, Christian A. Hübner, Christina L. McHenry, David W. Stockton, Gabriele Rammesmayer, James R. Lupski, Guillermo Antiñolo, Carmen Ayuso, Montserrat Baiget, Peter Gouras, John R. Heckenlively, Anneke Den Hollander, Samuel G. Jacobson, Richard A. Lewis, Paul A. Sieving, Bernd Wissinger, Suzanne Yzer, Eberhart Zrenner, Gerd Utermann, Andreas Gal

    منشور في 2005
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    Artigo
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  11. 11
    Central serous chorioretinopathy: Towards an evidence-based treatment guideline

    Central serous chorioretinopathy: Towards an evidence-based treatment guideline حسب Thomas J. van Rijssen, Elon H. C. van Dijk, Suzanne Yzer, Kyoko Ohno‐Matsui, Jan E.E. Keunen, Reinier O. Schlingemann, Sobha Sivaprasad, Giuseppe Querques, Susan M. Downes, Sascha Fauser, Carel B. Hoyng, Felice Cardillo Piccolino, Jay Chhablani, Timothy Y. Y. Lai, Andrew Lotery, Michael Larsen, Frank G. Holz, K. Bailey Freund, Lawrence A. Yannuzzi, Camiel J. F. Boon

    منشور في 2019
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    Revisão
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  12. 12
    Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis

    Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis حسب Suzanne Yzer, Bart P. Leroy, Elfride De Baere, Thomy de Ravel, Marijke N. Zonneveld, Krysta Voesenek, Ulrich Kellner, José P. Martinez Ciriano, Jan-Tjeerd H.N. de Faber, Klaus Rohrschneider, Ronald Roepman, Anneke I. den Hollander, J.R.M. Cruysberg, Franc ̧oise Meire, Ingele Casteels, Norka G. van Moll-Ramirez, Rando Allikmets, L. Ingeborgh van den Born, Frans P.M. Cremers

    منشور في 2006
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    Artigo
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  13. 13
    Central serous chorioretinopathy: An evidence-based treatment guideline

    Central serous chorioretinopathy: An evidence-based treatment guideline حسب Helena M. A. Feenstra, Elon H. C. van Dijk, Chui Ming Gemmy Cheung, Kyoko Ohno‐Matsui, Timothy Y. Y. Lai, Hideki Koizumi, Michael Larsen, Giuseppe Querques, Susan M. Downes, Suzanne Yzer, Mark P. Breazzano, Yousif Subhi, Ramin Tadayoni, Siegfried Priglinger, Laurenz Pauleikhoff, Clemens Lange, Anat Loewenstein, Roselie M.H. Diederen, Reinier O. Schlingemann, Carel B. Hoyng, Jay Chhablani, Frank G. Holz, Sobha Sivaprasad, Andrew Lotery, Lawrence A. Yannuzzi, K. Bailey Freund, Camiel J. F. Boon

    منشور في 2024
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    Revisão
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  14. 14
    Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis

    Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis حسب James Bainbridge, Manjit Mehat, Venki Sundaram, Scott Robbie, Susie E. Barker, Caterina Ripamonti, Anastasios Georgiadis, Freya M. Mowat, Stuart G. Beattie, Peter J. Gardner, Kecia L. Feathers, Vy Luong, Suzanne Yzer, Kamaljit S. Balaggan, Ananth C. Viswanathan, Thomy de Ravel, Ingele Casteels, Graham E. Holder, Nick Tyler, Fred W. Fitzke, Richard G. Weleber, Marko Nardini, Anthony T. Moore, Debra A. Thompson, Simon M. Petersen‐Jones, Michel Michaelides, L. Ingeborgh van den Born, Andrew Stockman, Alexander J. Smith, Gary S. Rubin, Robin R. Ali

    منشور في 2015
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