Entries of Charbel Issa, Peter on the publication server

Jolly, Jasleen K. , Wagner, Siegfried K., Martus, Peter, MacLaren, Robert E., Wilhelm, Barbara, Webster, Andrew R., Downes, Susan M., Charbel Issa, Peter, Kellner, Ulrich, Jägle, Herbert, Rüther, Klaus, Bertelsen, Mette, Bragadóttir, Ragnheiður, Prener Holtan, Josephine, van den Born, L. Ingeborgh, Sodi, Andrea, Virgili, Gianni, Gosheva, Mariya, Pach, Johanna, Zündorf, Ida, Zrenner, Eberhart and Gekeler, Florian (2019) Transcorneal Electrical Stimulation for the Treatment of Retinitis Pigmentosa: A Multicenter Safety Study of the OkuStim® System (TESOLA-Study). Ophthalmic Research 63 (3), pp. 234-243. Fulltext not available.

Brandl, Caroline , Schulz, Heidi, Charbel Issa, Peter, Birtel, Johannes, Bergholz, Richard, Lange, Clemens, Dahlke, Claudia, Zobor, Ditta, Weber, Bernhard and Stöhr, Heidi (2017) Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular Lesions. Genes 8 (170), pp. 1-14.

Neuhaus, Christine, Eisenberger, Tobias, Decker, Christian, Nagl, Sandra, Blank, Cornelia, Pfister, Markus, Kennerknecht, Ingo, Müller-Hofstede, Cornelie, Charbel Issa, Peter, Heller, Raoul, Beck, Bodo, Rüther, Klaus, Mitter, Diana, Rohrschneider, Klaus, Steinhauer, Ute, Korbmacher, Heike M., Huhle, Dagmar, Elsayed, Solaf M., Taha, Hesham M., Baig, Shahid M., Stöhr, Heidi, Preising, Markus, Markus, Susanne, Moeller, Fabian, Lorenz, Birgit, Nagel-Wolfrum, Kerstin, Khan, Arif O. and Bolz, Hanno J. (2017) Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome. Molecular Genetics & Genomic Medicine 5 (5), pp. 531-552. Fulltext not available.

Weber, Bernhard H. F. , Charbel Issa, Peter, Pauly, Diana, Herrmann, Philipp, Grassmann, Felix and Holz, Frank G. (2014) The Role of the Complement System in Age-Related Macular Degeneration. Deutsches Ärzteblatt international. Fulltext not available.

Gliem, Martin, Holz, Frank G., Stöhr, Heidi, Weber, Bernhard H. F. and Charbel Issa, Peter (2014) X-LINKED JUVENILE RETINOSCHISIS IN A CONSANGUINEOUS FAMILY. Retina 34 (12), pp. 2472-2478. Fulltext not available.