Empowering patients with high myopia: The significance of education
Ravenstijn, M., Jansen, R. C., Bois, G., Yzer, S., Klaver, C. C. W.
Published in Acta ophthalmologica (Oxford, England) (01.05.2024)
Published in Acta ophthalmologica (Oxford, England) (01.05.2024)
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Lipocalin 2 as a potential systemic biomarker for central serous chorioretinopathy
Matet, A, Jaworski, T, Bousquet, E, Canonica, J, Gobeaux, C, Daruich, A, Zhao, M, Zola, M, Meester-Smoor, M, Mohabati, D, Jaisser, F, Yzer, S, Behar-Cohen, F
Published in Scientific reports (19.11.2020)
Published in Scientific reports (19.11.2020)
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A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population
Yzer, S, van den Born, L I, Schuil, J, Kroes, H Y, van Genderen, M M, Boonstra, F N, van den Helm, B, Brunner, H G, Koenekoop, R K, Cremers, F P M
Published in Journal of medical genetics (01.09.2003)
Published in Journal of medical genetics (01.09.2003)
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Risk of Recurrence and Transition to Chronic Disease in Acute Central Serous Chorioretinopathy
Mohabati, Danial, Boon, Camiel J F, Yzer, Suzanne
Published in Clinical ophthalmology (Auckland, N.Z.) (01.01.2020)
Published in Clinical ophthalmology (Auckland, N.Z.) (01.01.2020)
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Mutations in the CEP290 ( NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis
den Hollander, Anneke I., Koenekoop, Robert K., Yzer, Suzanne, Lopez, Irma, Arends, Maarten L., Voesenek, Krysta E.J., Zonneveld, Marijke N., Strom, Tim M., Meitinger, Thomas, Brunner, Han G., Hoyng, Carel B., van den Born, L. Ingeborgh, Rohrschneider, Klaus, Cremers, Frans P.M.
Published in American journal of human genetics (01.09.2006)
Published in American journal of human genetics (01.09.2006)
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Clinical characteristics and long-term visual outcome of severe phenotypes of chronic central serous chorioretinopathy
Mohabati, Danial, van Rijssen, Thomas J, van Dijk, Elon Hc, Luyten, Gregorius Pm, Missotten, Tom O, Hoyng, Carel B, Yzer, Suzanne, Boon, Camiel Jf
Published in Clinical ophthalmology (Auckland, N.Z.) (01.01.2018)
Published in Clinical ophthalmology (Auckland, N.Z.) (01.01.2018)
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Clinical spectrum of severe chronic central serous chorioretinopathy and outcome of photodynamic therapy
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
Published in Clinical ophthalmology (Auckland, N.Z.) (01.01.2018)
Published in Clinical ophthalmology (Auckland, N.Z.) (01.01.2018)
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Journal Article
Ocular and extra-ocular features of patients with Leber congenital amaurosis and mutations in CEP290
Yzer, Suzanne, Hollander, Anneke I den, Lopez, Irma, Pott, Jan-Willem R, de Faber, Jan Tjeerd H N, Cremers, Frans P M, Koenekoop, Robert K, van den Born, L Ingeborgh
Published in Molecular vision (10.02.2012)
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Published in Molecular vision (10.02.2012)
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Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle
Thompson, Debra A., Janecke, Andreas R., Lange, Jessica, Feathers, Kecia L., Hübner, Christian A., McHenry, Christina L., Stockton, David W., Rammesmayer, Gabriele, Lupski, James R., Antinolo, Guillermo, Ayuso, Carmen, Baiget, Montserrat, Gouras, Peter, Heckenlively, John R., den Hollander, Anneke, Jacobson, Samuel G., Lewis, Richard A., Sieving, Paul A., Wissinger, Bernd, Yzer, Suzanne, Zrenner, Eberhart, Utermann, Gerd, Gal, Andreas
Published in Human molecular genetics (15.12.2005)
Published in Human molecular genetics (15.12.2005)
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Neovascular age-related macular degeneration without drusen in the fellow eye: clinical spectrum and therapeutic outcome
Chung, Wing H, van Dijk, Elon H C, Mohabati, Danial, Dijkman, Greet, Yzer, Suzanne, de Jong, Eiko K, Fauser, Sascha, Schlingemann, Reinier O, Hoyng, Carel B, Boon, Camiel J F
Published in Clinical ophthalmology (Auckland, N.Z.) (01.01.2017)
Published in Clinical ophthalmology (Auckland, N.Z.) (01.01.2017)
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Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis
Yzer, Suzanne, Leroy, Bart P, De Baere, Elfride, de Ravel, Thomy J, Zonneveld, Marijke N, Voesenek, Krysta, Kellner, Ulrich, Ciriano, Jose P. Martinez, de Faber, Jan-Tjeerd H. N, Rohrschneider, Klaus, Roepman, Ronald, den Hollander, Anneke I, Cruysberg, Johannes R, Meire, Francoise, Casteels, Ingele, van Moll-Ramirez, Norka G, Allikmets, Rando, van den Born, L. Ingeborgh, Cremers, Frans P. M
Published in Investigative ophthalmology & visual science (01.03.2006)
Published in Investigative ophthalmology & visual science (01.03.2006)
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Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa
KLEVERING, B. Jeroen, YZER, Suzanne, ROHRSCHNEIDER, Klaus, ZONNEVELD, Marijke, ALLIKMETS, Rando, VAN DEN BORN, L. Ingeborgh, MAUGERI, Alessandra, HOYNG, Carel B, CREMERS, Frans P. M
Published in European journal of human genetics : EJHG (01.12.2004)
Published in European journal of human genetics : EJHG (01.12.2004)
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Journal Article
From gene to disease; Leber congenital amaurosis (LCA)
Yzer, S, van den Born, L I, Cremers, F P M, den Hollander, A I
Published in Nederlands tijdschrift voor geneeskunde (15.10.2005)
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Published in Nederlands tijdschrift voor geneeskunde (15.10.2005)
Journal Article
Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle
Thompson, Debra A., Janecke, Andreas R., Lange, Jessica, Feathers, Kecia L., Hübner, Christian A., McHenry, Christina L., Stockton, David W., Rammesmayer, Gabriele, Lupski, James R., Antinolo, Guillermo, Ayuso, Carmen, Baiget, Montserrat, Gouras, Peter, Heckenlively, John R., den Hollander, Anneke, Jacobson, Samuel G., Lewis, Richard A., Sieving, Paul A., Wissinger, Bernd, Yzer, Suzanne, Zrenner, Eberhart, Utermann, Gerd, Gal, Andreas
Published in Human molecular genetics (01.05.2006)
Published in Human molecular genetics (01.05.2006)
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