Fundus Autofluorescence and mfERG for Early Detection of Retinal Alterations in Patients Using Chloroquine/Hydroxychloroquine von Kellner, Ulrich, Renner, Agnes B, Tillack, Hilmar

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Clinical Heterogeneity in Autosomal Recessive Bestrophinopathy with Biallelic Mutations in the BEST1 Gene von Hufendiek, Karsten, Hufendiek, Katerina, Jägle, Herbert, Stöhr, Heidi, Book, Marius, Spital, Georg, Rustambayova, Günay, Framme, Carsten, Weber, Bernhard H F, Renner, Agnes B, Kellner, Ulrich

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TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, Isabelle, Kohl, Susanne, Leroy, Bart P., Munier, Francis L., Guillonneau, Xavier, Mohand-Saïd, Saddek, Bujakowska, Kinga, Nandrot, Emeline F., Lorenz, Birgit, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Bernd, Antje, Antonio, Aline, Moskova-Doumanova, Veselina, Lancelot, Marie-Elise, Poloschek, Charlotte M., Drumare, Isabelle, Defoort-Dhellemmes, Sabine, Wissinger, Bernd, Léveillard, Thierry, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Berger, Wolfgang, Jacobson, Samuel G., Zrenner, Eberhart, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina

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A subgroup of age-related macular degeneration is associated with mono-allelic sequence variants in the ABCA4 gene von Fritsche, Lars G, Fleckenstein, Monika, Fiebig, Britta S, Schmitz-Valckenberg, Steffen, Bindewald-Wittich, Almut, Keilhauer, Claudia N, Renner, Agnes B, Mackensen, Friederike, Mößner, Andreas, Pauleikhoff, Daniel, Adrion, Christine, Mansmann, Ulrich, Scholl, Hendrik P N, Holz, Frank G, Weber, Bernhard H F

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Gray matter alterations in visual cortex of patients with loss of central vision due to hereditary retinal dystrophies von Plank, Tina, Frolo, Jozef, Brandl-Rühle, Sabine, Renner, Agnes B., Hufendiek, Karsten, Helbig, Horst, Greenlee, Mark W.

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Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis Pigmentosa von Langmann, Thomas, Di Gioia, Silvio Alessandro, Rau, Isabella, Stöhr, Heidi, Maksimovic, Nela S., Corbo, Joseph C., Renner, Agnes B., Zrenner, Eberhart, Kumaramanickavel, Govindasamy, Karlstetter, Marcus, Arsenijevic, Yvan, Weber, Bernhard H.F., Gal, Andreas, Rivolta, Carlo

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Recurrent episodes of night blindness in a patient with short bowel syndrome von Renner, Agnes B., Dietrich-Ntoukas, Tina, Jägle, Herbert

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Neural correlates of visual search in patients with hereditary retinal dystrophies von Plank, Tina, Frolo, Jozef, Farzana, Fatima, Brandl-Rühle, Sabine, Renner, Agnes B., Greenlee, Mark W.

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Yoga intervention and reminder e-mails for reducing cancer-related fatigue - a study protocol of a randomized controlled trial von Zetzl, Teresa, Schuler, Michael, Renner, Agnes, Jentschke, Elisabeth, van Oorschot, Birgitt

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Phenotypic Variability and Long-term Follow-up of Patients With Known and Novel PRPH2/RDS Gene Mutations von Renner, Agnes B, Fiebig, Britta S, Weber, Bernhard H.F, Wissinger, Bernd, Andreasson, Sten, Gal, Andreas, Cropp, Elke, Kohl, Susanne, Kellner, Ulrich

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Ten-year follow-up of two unrelated patients with Müller cell sheen dystrophy and first report of successful vitrectomy von Renner, Agnes B., Radeck, Viola, Kellner, Ulrich, Jägle, Herbert, Helbig, Horst

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Mutation Analysis Identifies GUCY2D as the Major Gene Responsible for Autosomal Dominant Progressive Cone Degeneration von Kitiratschky, Veronique B. D, Wilke, Robert, Renner, Agnes B, Kellner, Ulrich, Vadala, Maria, Birch, David G, Wissinger, Bernd, Zrenner, Eberhart, Kohl, Susanne

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Gyrate atrophy: clinical and genetic findings in a female without arginine-restricted diet during her first 39 years of life and report of a new OAT gene mutation von Renner, Agnes B., Walter, Andreas, Fiebig, Britta S., Jägle, Herbert

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Choroideremia: Variability of Clinical and Electrophysiological Characteristics and First Report of a Negative Electroretinogram von Renner, Agnes B., Kellner, Ulrich, Cropp, Elke, Preising, Markus N., MacDonald, Ian M., van den Hurk, José A.J.M., Cremers, Frans P.M., Foerster, Michael H.

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Late Onset is Common in Best Macular Dystrophy Associated with VMD2 Gene Mutations von Renner, Agnes B., Tillack, Hilmar, Kraus, Hannelore, Krämer, Franziska, Mohr, Nicole, Weber, Bernhard H.F., Foerster, Michael H., Kellner, Ulrich

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ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies von Kitiratschky, Veronique B D, Grau, Tanja, Bernd, Antje, Zrenner, Eberhart, Jägle, Herbert, Renner, Agnes B, Kellner, Ulrich, Rudolph, Günther, Jacobson, Samuel G, Cideciyan, Artur V, Schaich, Simone, Kohl, Susanne, Wissinger, Bernd

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Dysfunction of transmission in the inner retina: incidence and clinical causes of negative electroretinogram von Renner, Agnes B, Kellner, Ulrich, Cropp, Elke, Foerster, Michael H

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ERG variability in X-linked congenital retinoschisis patients with mutations in the RS1 gene and the diagnostic importance of fundus autofluorescence and OCT von Renner, Agnes B., Kellner, Ulrich, Fiebig, Britta, Cropp, Elke, Foerster, Michael H., Weber, Bernhard H. F.

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Yoga effectively reduces fatigue and symptoms of depression in patients with different types of cancer von Zetzl, Teresa, Renner, Agnes, Pittig, Andre, Jentschke, Elisabeth, Roch, Carmen, van Oorschot, Birgitt

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Variety of genotypes in males diagnosed as dichromatic on a conventional clinical anomaloscope von NEITZ, MAUREEN, CARROLL, JOSEPH, RENNER, AGNES, KNAU, HOLGER, WERNER, JOHN S., NEITZ, JAY

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