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- University of Regensburg (5)
- Medicine (5)
- Lehrstuhl für Humangenetik (5)
- Medicine (5)
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Grassmann, Felix and Harsch, Sebastian and Brandl, Caroline and Kiel, Christina and Nuernberg, Peter and Toliat, Mohammad R. and Fleckenstein, Monika and Pfau, Maximilian and Schmitz-Valckenberg, Steffen and Holz, Frank G. and Chew, Emily Y. and Swaroop, Anand and Ratnapriya, Rinki and Klein, Michael L. and Mulyukov, Zufar and Zamiri, Parisa and Weber, Bernhard H. F. (2019) Assessment of Novel Genome-Wide Significant Gene Loci and Lesion Growth in Geographic Atrophy Secondary to Age-Related Macular Degeneration. JAMA OPHTHALMOLOGY, 137 (8). pp. 867-876. ISSN 2168-6165, 2168-6173
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Keilhauer, Claudia N. and Meigen, Thomas and Weber, Bernhard H. F. (2006) Clinical findings in a multigeneration familly with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/RDS gene. ARCHIVES OF OPHTHALMOLOGY, 124 (7). pp. 1020-1027. ISSN 0003-9950
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Renner, Agnes B. and Fiebig, Britta S. and Cropp, Elke and Weber, Bernhard H. F. and Kellner, Ulrich (2009) Progression of Retinal Pigment Epithelial Alterations During Long-term Follow-up in Female Carriers of Choroideremia and Report of a Novel CHM Mutation. ARCHIVES OF OPHTHALMOLOGY, 127 (7). pp. 907-912. ISSN 0003-9950, 1538-3601
Runhart, Esmee H. and Khan, Mubeen and Cornelis, Stephanie S. and Roosing, Susanne and Del Pozo-Valero, Marta and Lamey, Tina M. and Liskova, Petra and Roberts, Lisa and Stoehr, Heidi and Klaver, Caroline C. W. and Hoyng, Carel B. and Cremers, Frans P. M. and Dhaenens, Claire-Marie (2020) Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease. JAMA OPHTHALMOLOGY, 138 (10). pp. 1035-1042. ISSN 2168-6165, 2168-6173
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Winner, Beate and Uyanik, Goekhan and Gross, Claudia and Lange, Max and Schulte-Mattler, Wilhelm and Schuierer, Gerhard and Marienhagen, Joerg and Hehr, Ute and Winkler, Juergen (2004) Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11). ARCHIVES OF NEUROLOGY, 61 (1). pp. 117-121. ISSN 0003-9942, 1538-3687

