Number of items: 3.
2019
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.
2017
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.
This list was generated on Thu Dec 12 03:20:51 2024 CET.