Browsing Universitätsbibliographie by Author "Hipp, Stephanie"

Now showing items 1-7 of 7

Artificial vision with wirelessly powered subretinal electronic implant alpha-IMS

Stingl, Katarina; Bartz-Schmidt, Karl Ulrich; Besch, Dorothea; Braun, Angelika; Bruckmann, Anna; Gekeler, Florian; Greppmaier, Udo; Hipp, Stephanie; Hoertdoerfer, Gernot; Kernstock, Christoph; Koitschev, Assen; Kusnyerik, Akos; Sachs, Helmut; Schatz, Andreas; Stingl, Krunoslav T.; Peters, Tobias; Wilhelm, Barbara; Zrenner, Eberhart (2013)
Clinical Characteristics of Rod and Cone Photoreceptor Dystrophies in Patients With Mutations in the C8orf37 Gene

van Huet, Ramon A. C.; Estrada-Cuzcano, Alejandro; Banin, Eyal; Rotenstreich, Ygal; Hipp, Stephanie; Kohl, Susanne; Hoyng, Carel B.; den Hollander, Anneke I.; Collin, Rob W. J.; Klevering, B. Jeroen (2013)
Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study

Stingl, Katarina; Kurtenbach, Anne; Hahn, Gesa; Kernstock, Christoph; Hipp, Stephanie; Zobor, Ditta; Kohl, Susanne; Bonnet, Crystel; Mohand-Said, Saddek; Audo, Isabelle; Fakin, Ana; Hawlina, Marko; Testa, Francesco; Simonelli, Francesca; Petit, Christine; Sahel, Jose-Alain; Zrenner, Eberhart (2019)
Mutations in C8orf37, Encoding a Ciliary Protein, are Associated with Autosomal-Recessive Retinal Dystrophies with Early Macular Involvement

Estrada-Cuzcano, Alejandro; Neveling, Kornelia; Kohl, Susanne; Banin, Eyal; Rotenstreich, Ygal; Sharon, Dror; Falik-Zaccai, Tzipora C.; Hipp, Stephanie; Roepman, Ronald; Wissinger, Bernd; Letteboer, Stef J. F.; Mans, Dorus A.; Blokland, Ellen A. W.; Kwint, Michael P.; Gijsen, Sabine J.; van Huet, Ramon A. C.; Collin, Rob W. J.; Scheffer, H.; Veltman, Joris A.; Zrenner, Eberhart; den Hollander, Anneke I.; Klevering, B. Jeroen; Cremers, Frans P. M. (2012)
Phenotype Variations Caused by Mutations in the RP1L1 Gene in a Large Mainly German Cohort

Zobor, Ditta; Zobor, Gergely; Hipp, Stephanie; Baumann, Britta; Weisschuh, Nicole; Biskup, Saskia; Sliesoraityte, Ieva; Zrenner, Eberhart; Kohl, Susanne (2018)
Phenotype variations of retinal dystrophies caused by mutations in the RLBP1 gene

Hipp, Stephanie; Zobor, Gergely; Gloeckle, Nicola; Mohr, Julia; Kohl, Susanne; Zrenner, Eberhart; Weisschuh, Nicole; Zobor, Ditta (2015)
Usher Syndrome and Color Vision

Kurtenbach, Anne; Hahn, Gesa; Kernstock, Christoph; Hipp, Stephanie; Zobor, Ditta; Stingl, Katarina; Kohl, Susanne; Bonnet, Crystel; Mohand-Said, Saddek; Sliesoraityte, Ieva; Sahel, Jose-Alain; Audo, Isabelle; Fakin, Ana; Hawlina, Marko; Testa, Francesco; Simonelli, Francesca; Petit, Christine; Zrenner, Eberhart (2018)

Now showing items 1-7 of 7

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