Items where Author is "Issa, Peter Charbel"

Article

Jolly, Jasleen K. and Wagner, Siegfried K. and Martus, Peter and MacLaren, Robert E. and Wilhelm, Barbara and Webster, Andrew R. and Downes, Susan M. and Issa, Peter Charbel and Kellner, Ulrich and Jaegle, Herbert and Ruether, Klaus and Bertelsen, Mette and Bragadottir, Ragnheidur and Holtan, Josephine Prener and van den Born, Ingeborgh and Sodi, Andrea and Virgili, Gianni and Gosheva, Mariya and Pach, Johanna and Zuendorf, Ida and Zrenner, Eberhart and Gekeler, Florian (2020) Transcorneal Electrical Stimulation for the Treatment of Retinitis Pigmentosa: A Multicenter Safety Study of the OkuStim (R) System (TESOLA-Study). OPHTHALMIC RESEARCH, 63 (3). pp. 234-243. ISSN 0030-3747, 1423-0259

Brandl, Caroline and Schulz, Heidi L. and Issa, Peter Charbel and Birtel, Johannes and Bergholz, Richard and Lange, Clemens and Dahlke, Claudia and Zobor, Ditta and Weber, Bernhard H. F. and Stoehr, Heidi (2017) Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular Lesions. GENES, 8 (7). ISSN 2073-4425

Neuhaus, Christine and Eisenberger, Tobias and Decker, Christian and Nagl, Sandra and Blank, Cornelia and Pfister, Markus and Kennerknecht, Ingo and Mueller-Hofstede, Cornelie and Issa, Peter Charbel and Heller, Raoul and Beck, Bodo and Ruether, Klaus and Mitter, Diana and Rohrschneider, Klaus and Steinhauer, Ute and Korbmacher, Heike M. and Huhle, Dagmar and Elsayed, Solaf M. and Taha, Hesham M. and Baig, Shahid M. and Stoehr, Heidi and Preising, Markus and Markus, Susanne and Moeller, Fabian and Lorenz, Birgit and Nagel-Wolfrum, Kerstin and 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. ISSN 2324-9269

Mueller, Philipp L. and Gliem, Martin and Mangold, Elisabeth and Bolz, Hanno J. and Finger, Robert P. and McGuinness, Myra and Betz, Christian and Jiang, Zhichun and Weber, Bernhard H. F. and MacLaren, Robert E. and Holz, Frank G. and Radu, Roxana A. and Issa, Peter Charbel (2015) Monoallelic ABCA4 Mutations Appear Insufficient to Cause Retinopathy: A Quantitative Autofluorescence Study. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 56 (13). pp. 8179-8186. ISSN 0146-0404, 1552-5783

Gliem, Martin and Mueller, Philipp L. and Mangold, Elisabeth and Bolz, Hanno J. and Stoehr, Heidi and Weber, Bernhard H. F. and Holz, Frank G. and Issa, Peter Charbel (2015) Reticular Pseudodrusen in Sorsby Fundus Dystrophy. OPHTHALMOLOGY, 122 (8). pp. 1555-1562. ISSN 0161-6420, 1549-4713

Gliem, Martin and Mueller, Philipp L. and Mangold, Elisabeth and Holz, Frank G. and Bolz, Hanno J. and Stoehr, Heidi and Weber, Bernhard H. F. and Issa, Peter Charbel (2015) Sorsby Fundus Dystrophy: Novel Mutations, Novel Phenotypic Characteristics, and Treatment Outcome. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 56 (4). pp. 2664-2676. ISSN 0146-0404, 1552-5783

Weber, Bernhard H. F. and Issa, Peter Charbel and Pauly, Diana and Herrmann, Philipp and Grassmann, Felix and Holz, Frank G. (2014) The Role of the Complement System in Age-Related Macular Degeneration. DEUTSCHES ARZTEBLATT INTERNATIONAL, 111 (8). ISSN 1866-0452

Gliem, Martin and Holz, Frank G. and Stoehr, Heidi and Weber, Bernhard H. F. and Issa, Peter Charbel (2014) X-LINKED JUVENILE RETINOSCHISIS IN A CONSANGUINEOUS FAMILY Phenotypic Variability and Report of a Homozygous Female Patient. RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 34 (12). pp. 2472-2478. ISSN 0275-004X, 1539-2864

Lauer, Nadine and Mihlan, Michael and Hartmann, Andrea and Schloetzer-Schrehardt, Ursula and Keilhauer, Claudia and Scholl, Hendrik P. N. and Issa, Peter Charbel and Holz, Frank and Weber, Bernhard H. F. and Skerka, Christine and Zipfel, Peter F. (2011) Complement Regulation at Necrotic Cell Lesions Is Impaired by the Age-Related Macular Degeneration-Associated Factor-H His(402) Risk Variant. JOURNAL OF IMMUNOLOGY, 187 (8). pp. 4374-4383. ISSN 0022-1767

Scholl, Hendrik P. N. and Issa, Peter Charbel and Walier, Maja and Janzer, Stefanie and Pollok-Kopp, Beatrix and Boerncke, Florian and Fritsche, Lars G. and Chong, Ngaihang V. and Fimmers, Rolf and Wienker, Thomas and Holz, Frank G. and Weber, Bernhard H. F. and Oppermann, Martin (2008) Systemic Complement Activation in Age-Related Macular Degeneration. PLOS ONE, 3 (7): e2593. ISSN 1932-6203