Chronic central serous chorioretinopathy: long-term follow-up and vision-related quality of life von Breukink, Myrte B, Dingemans, Alexander Jm, den Hollander, Anneke I, Keunen, Jan Ee, MacLaren, Robert E, Fauser, Sascha, Querques, Giuseppe, Hoyng, Carel B, Downes, Susan M, Boon, Camiel Jf

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Clinical characteristics and long-term visual outcome of severe phenotypes of chronic central serous chorioretinopathy von Mohabati, Danial, van Rijssen, Thomas J, van Dijk, Elon Hc, Luyten, Gregorius Pm, Missotten, Tom O, Hoyng, Carel B, Yzer, Suzanne, Boon, Camiel Jf

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Self-Supervised Learning for Improved Optical Coherence Tomography Detection of Macular Telangiectasia Type 2 von Gholami, Shahrzad, Scheppke, Lea, Kshirsagar, Meghana, Wu, Yue, Dodhia, Rahul, Bonelli, Roberto, Leung, Irene, Sallo, Ferenc B, Muldrew, Alyson, Jamison, Catherine, Peto, Tunde, Lavista Ferres, Juan, Weeks, William B, Friedlander, Martin, Lee, Aaron Y

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Extramacular drusen are highly associated with age-related macular degeneration, but not with CFH and ARMS2 genotypes von Ersoy, L, Schick, T, de Graft, D, Felsch, M, Hoyng, CB, den Hollander, AI, Kirchhof, B, Fauser, S, Liakopoulos, S

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A genetic variant in NRP1 is associated with worse response to ranibizumab treatment in neovascular age-related macular degeneration von Lorés-Motta, Laura, van Asten, Freekje, Muether, Philipp S, Smailhodzic, Dzenita, Groenewoud, Joannes M, Omar, Amer, Chen, John, Koenekoop, Robert K, Fauser, Sascha, Hoyng, Carel B, den Hollander, Anneke I, de Jong, Eiko K

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Clinical spectrum of severe chronic central serous chorioretinopathy and outcome of photodynamic therapy von Mohabati, Danial, van Dijk, Elon Hc, van Rijssen, Thomas J, de Jong, Eiko K, Breukink, Myrte B, Martinez-Ciriano, Jose P, Dijkman, Greet, Hoyng, Carel B, Fauser, Sascha, Yzer, Suzanne, Boon, Camiel Jf

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Mutations in the ABCA4 ( ABCR) Gene Are the Major Cause of Autosomal Recessive Cone-Rod Dystrophy von Maugeri, Alessandra, Klevering, B. Jeroen, Rohrschneider, Klaus, Blankenagel, Anita, Brunner, Han G., Deutman, August F., Hoyng, Carel B., Cremers, Frans P.M.

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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia von KOHL, Susanne, VARSANYI, Balazs, JURKLIES, Bernhard, FARKAS, Agnes, ANDREASSON, Sten, WELEBER, Richard G, JACOBSON, Samuel G, RUDOLPH, Günther, CASTELLAN, Claudio, DOLLFUS, Helene, LEGIUS, Eric, ANASTASI, Mario, ANTUNES, Gesine Abadin, BITOUN, Pierre, LEV, Dorit, SIEVING, Paul A, MUNIER, Francis L, ZRENNER, Eberhart, SHARPE, Lindsay T, CREMERS, Frans P. M, WISSINGER, Bernd, BAUMANN, Britta, HOYNG, Carel B, JÄGLE, Herbert, ROSENBERG, Thomas, KELLNER, Ulrich, LORENZ, Birgit, SALATI, Roberto

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Genotyping microarray (gene chip) for the ABCR (ABCA4) gene von Jaakson, K., Zernant, J., Külm, M., Hutchinson, A., Tonisson, N., Glavač, D., Ravnik‐Glavač, M., Hawlina, M., Meltzer, M.R., Caruso, R.C., Testa, F., Maugeri, A., Hoyng, C.B., Gouras, P., Simonelli, F., Lewis, R.A., Lupski, J.R., Cremers, F.P.M., Allikmets, R.

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Mutations in GRM6 Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram von Zeitz, Christina, van Genderen, Maria, Neidhardt, John, Luhmann, Ulrich F. O, Hoeben, Frank, Forster, Ursula, Wycisk, Katharina, Matyas, Gabor, Hoyng, Carel B, Riemslag, Frans, Meire, Francoise, Cremers, Frans P. M, Berger, Wolfgang

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CRB1 mutation spectrum in inherited retinal dystrophies von den Hollander, Anneke I., Davis, Jason, van der Velde-Visser, Saskia D., Zonneveld, Marijke N., Pierrottet, Chiara O., Koenekoop, Robert K., Kellner, Ulrich, van den Born, L. Ingeborgh, Heckenlively, John R., Hoyng, Carel B., Handford, Penny A., Roepman, Ronald, Cremers, Frans P.M.

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CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders von Wissinger, Bernd, Gamer, Daphne, Jägle, Herbert, Giorda, Roberto, Marx, Tim, Mayer, Simone, Tippmann, Sabine, Broghammer, Martina, Jurklies, Bernhard, Rosenberg, Thomas, Jacobson, Samuel G., Sener, E. Cumhur, Tatlipinar, Sinan, Hoyng, Carel B., Castellan, Claudio, Bitoun, Pierre, Andreasson, Sten, Rudolph, Günter, Kellner, Ulrich, Lorenz, Birgit, Wolff, Gerhard, Verellen-Dumoulin, Christine, Schwartz, Marianne, Cremers, Frans P.M., Apfelstedt-Sylla, Eckart, Zrenner, Eberhart, Salati, Roberto, Sharpe, Lindsay T., Kohl, Susanne

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Alteration of retinal layers in healthy subjects over 60 years of age until nonagenarians von Altay, Lebriz, Jahn, Cheryl, Arikan Yorgun, Mücella, Caramoy, Albert, Schick, Tina, Hoyng, Carel B, den Hollander, Anneke I, Fauser, Sascha

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The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene von Klevering, B Jeroen, Deutman, August F, Maugeri, Alessandra, Cremers, Frans P M, Hoyng, Carel B

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Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13) von MCKIE, Arthur B, MCHALE, John C, MACKEY, David A, BHATTACHARYA, Shomi S, BIRD, Alan C, MARKHAM, Alexander F, INGLEHEARN, Chris F, KEEN, T. Jeffrey, TARTTELIN, Emma E, GOLIATH, Rene, VAN LITH-VERHOEVEN, Janneke J. C, GREENBERG, Jacquie, RAMESAR, Rajkumar S, HOYNG, Carel B, CREMERS, Frans P. M

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A Prospective, randomized trial of pyrimethamine and azithromycin vs pyrimethamine and sulfadiazine for the treatment of ocular toxoplasmosis von BOSCH-DRIESSEN, Lotje H, VERBRAAK, Frank D, SUTTORP-SCHULTEN, Maria S. A, VAN RUYVEN, Rutger L. J, KLOK, Anne Marie, HOYNG, Carel B, ROTHOVA, Aniki

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A Novel Mutation in the ELOVL4 Gene Causes Autosomal Dominant Stargardt-like Macular Dystrophy von Maugeri, Alessandra, Meire, Francoise, Hoyng, Carel B, Vink, Carolien, Van Regemorter, Nicole, Karan, Goutam, Yang, Zhenglin, Cremers, Frans P. M, Zhang, Kang

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Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12) von Cremers, Frans P.M, den Hollander, Anneke I, ten Brink, Jacoline B, de Kok, Yvette J.M, van Soest, Simone, van den Born, L. Ingeborgh, van Driel, Marc A, van de Pol, Dorien J.R, Payne, Annette M, Bhattacharya, Shomi S, Kellner, Ulrich, Hoyng, Carel B, Westerveld, Andries, Brunner, Han G, Bleeker-Wagemakers, Elisabeth M, Deutman, August F, Heckenlively, John R, Bergen, Arthur A.B

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Autosomal Recessive Retinitis Pigmentosa and Cone-rod Dystrophy Caused by Splice Site Mutations in the Stargardt's Disease Gene ABCR von Cremers, Frans P. M., van de Pol, Dorien J. R., van Driel, Marc, den Hollander, Anneke I., van Haren, Frank J. J., Knoers, Nine V. A. M., Tijmes, Nel, Bergen, Arthur A. B., Rohrschneider, Klaus, Blankenagel, Anita, Pinckers, Alfred J. L. G., Deutman, August F., Hoyng, Carel B.

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Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 ( CRB1) Gene von Hollander, Anneke I. den, Heckenlively, John R., van den Born, L. Ingeborgh, de Kok, Yvette J.M., van der Velde-Visser, Saskia D., Kellner, Ulrich, Jurklies, Bernhard, van Schooneveld, Mary J., Blankenagel, Anita, Rohrschneider, Klaus, Wissinger, Bernd, Cruysberg, Johan R.M., Deutman, August F., Brunner, Han G., Apfelstedt-Sylla, Eckart, Hoyng, Carel B., Cremers, Frans P.M.

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