Organotypic Cultures of Adult Mouse Retina: Morphologic Changes and Gene Expression von Müller, Brigitte, Wagner, Franziska, Lorenz, Birgit, Stieger, Knut

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Creation of different bioluminescence resonance energy transfer based biosensors with high affinity to VEGF von Stumpf, Constanze, Wimmer, Tobias, Lorenz, Birgit, Stieger, Knut

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Motor and Visual-spatial Cognitive Abilities in Children Treated for Infantile Esotropia von Dillmann, Julia, Freitag, Claudia, Lorenz, Birgit, Holve, Kerstin, Schweinfurth, Silke, Schwarzer, Gudrun

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Biallelic mutations in l-dopachrome tautomerase (DCT) cause infantile nystagmus and oculocutaneous albinism von Volk, Alexander E., Hedergott, Andrea, Preising, Markus, Rading, Sebastian, Fricke, Julia, Herkenrath, Peter, Nürnberg, Peter, Altmüller, Janine, von Ameln, Simon, Lorenz, Birgit, Neugebauer, Antje, Karsak, Meliha, Kubisch, Christian

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Recurrent heterozygous PAX6 missense variants cause severe bilateral microphthalmia via predictable effects on DNA–protein interaction von Williamson, Kathleen A., Hall, H. Nikki, Owen, Liusaidh J., Livesey, Benjamin J., Hanson, Isabel M., Adams, G., Bodek, Simon, Calvas, Patrick, Castle, Bruce, Clarke, Michael, Deng, Alexander T., Edery, Patrick, Fisher, Richard, Gillessen-Kaesbach, Gabriele, Heon, Elise, Hurst, Jane, Josifova, Dragana, Lorenz, Birgit, McKee, Shane, Meire, Francoise, Moore, Anthony T., Parker, Michael, Reiff, Charlotte M., Self, Jay, Tobias, Edward S., Verheij, Joke B., Willems, Marjolaine, Williams, Denise, van Heyningen, Veronica, Marsh, Joseph A., FitzPatrick, David R.

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Fundus Albipunctatus Associated with Compound Heterozygous Mutations in RPE65 von Schatz, Patrik, MD, PhD, Preising, Markus, PhD, Lorenz, Birgit, MD, PhD, Sander, Birgit, PhD, Larsen, Michael, MD, DMSc, Rosenberg, Thomas, MD

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Optimizing Measurement of Vascular Endothelial Growth Factor in Small Blood Samples of Premature Infants von Lopez Yomayuza, Claudia C., Preissner, Klaus T., Lorenz, Birgit, Stieger, Knut

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Functional Antibodies Targeting IsaA of Staphylococcus aureus Augment Host Immune Response and Open New Perspectives for Antibacterial Therapy von LORENZ, Udo, LORENZ, Birgit, SCHMITTER, Tim, STREKER, Karin, ERCK, Christian, WEHLAND, Jürgen, NICKEL, Joachim, ZIMMERMANN, Bastian, OHLSEN, Knut

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Detection of Intact rAAV Particles up to 6 Years After Successful Gene Transfer in the Retina of Dogs and Primates von Stieger, Knut, Schroeder, Josef, Provost, Nathalie, Mendes-Madeira, Alexandra, Belbellaa, Brahim, Meur, Guylène Le, Weber, Michel, Deschamps, Jack-Yves, Lorenz, Birgit, Moullier, Philippe, Rolling, Fabienne

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Genotyping Microarray (Disease Chip) for Leber Congenital Amaurosis: Detection of Modifier Alleles von Zernant, Jana, Kulm, Maigi, Dharmaraj, Sharola, den Hollander, Anneke I, Perrault, Isabelle, Preising, Markus N, Lorenz, Birgit, Kaplan, Josseline, Cremers, Frans P. M, Maumenee, Irene, Koenekoop, Robert K, Allikmets, Rando

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Mutation spectrum and splicing variants in the OPA1 gene von DELETTRE, Cécile, GRIFFOIN, Jean-Michel, KAPLAN, Josseline, DOLLFUS, Hélène, LORENZ, Birgit, FAIVRE, Laurence, LENAERS, Guy, BELENGUER, Pascale, HAMEL, Christian P

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Immuno-histochemical analysis of rod and cone reaction to RPE65 deficiency in the inferior and superior canine retina von Klein, Daniela, Mendes-Madeira, Alexandra, Schlegel, Patrice, Rolling, Fabienne, Lorenz, Birgit, Haverkamp, Silke, Stieger, Knut

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Feasibility and outcome of automated kinetic perimetry in children von Wilscher, Stephanie, Wabbels, Bettina, Lorenz, Birgit

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Fundus Autofluorescence in Carriers of Choroideremia and Correlation with Electrophysiologic and Psychophysical Data von Preising, Markus N., PhD, Wegscheider, Erika, MD, Friedburg, Christoph, MD, Poloschek, Charlotte M., MD, Wabbels, Bettina K., MD, Lorenz, Birgit, MD

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CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders von Wissinger, Bernd, Gamer, Daphne, Jägle, Herbert, Giorda, Roberto, Marx, Tim, Mayer, Simone, Tippmann, Sabine, Broghammer, Martina, Jurklies, Bernhard, Rosenberg, Thomas, Jacobson, Samuel G., Sener, E. Cumhur, Tatlipinar, Sinan, Hoyng, Carel B., Castellan, Claudio, Bitoun, Pierre, Andreasson, Sten, Rudolph, Günter, Kellner, Ulrich, Lorenz, Birgit, Wolff, Gerhard, Verellen-Dumoulin, Christine, Schwartz, Marianne, Cremers, Frans P.M., Apfelstedt-Sylla, Eckart, Zrenner, Eberhart, Salati, Roberto, Sharpe, Lindsay T., Kohl, Susanne

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A Comprehensive Survey of Sequence Variation in the ABCA4 ( ABCR) Gene in Stargardt Disease and Age-Related Macular Degeneration von Rivera, Andrea, White, Karen, Stöhr, Heidi, Steiner, Klaus, Hemmrich, Nadine, Grimm, Timo, Jurklies, Bernhard, Lorenz, Birgit, Scholl, Hendrik P.N., Apfelstedt-Sylla, Eckhart, Weber, Bernhard H.F.

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FOXL2 and BPES: Mutational Hotspots, Phenotypic Variability, and Revision of the Genotype-Phenotype Correlation von De Baere, Elfride, Beysen, Diane, Oley, Christine, Lorenz, Birgit, Cocquet, Julie, De Sutter, Paul, Devriendt, Koen, Dixon, Michael, Fellous, Marc, Fryns, Jean-Pierre, Garza, Arturo, Jonsrud, Christoffer, Koivisto, Pasi A., Krause, Amanda, Leroy, Bart P., Meire, Françoise, Plomp, Astrid, Van Maldergem, Lionel, De Paepe, Anne, Veitia, Reiner, Messiaen, Ludwine

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Characterization of the biological anti-staphylococcal functionality of hUK-66 IgG1, a humanized monoclonal antibody as substantial component for an immunotherapeutic approach von Oesterreich, Babett, Lorenz, Birgit, Schmitter, Tim, Kontermann, Roland, Zenn, Michael, Zimmermann, Bastian, Haake, Markus, Lorenz, Udo, Ohlsen, Knut

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Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy von Kumaramanickavel, Govindasamy, Rathmann, Michaela, Denton, Michael J, Srikumari, C.R. Srisailapathy, Gu, Su-min, Thompson, Debra A, Lorenz, Birgit, Finckh, Ulrich, Murthy, K.R, Gal, Andreas, Nicoletti, Aileen

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The Brückner Transillumination Test von Gräf, Michael, MD, Alhammouri, Qasem, MD, Vieregge, Christian, Lorenz, Birgit, MD

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