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Anzahl der Publikationen: 3
Zeitschriftenartikel
Solaki, Maria; Baumann, Britta; Reuter, Peggy; Andreasson, Sten; Audo, Isabelle; Ayuso, Carmen; Balousha, Ghassan; Benedicenti, Francesco; Birch, David; Bitoun, Pierre; Blain, Delphine; Bocquet, Beatrice; Branham, Kari; Catala-Mora, Jaume; De Baere, Elfride; Dollfus, Helene; Falana, Mohammed; Giorda, Roberto; Golovleva, Irina; Gottlob, Irene; Heckenlively, John R.; Jacobson, Samuel G.; Jones, Kaylie; Jaegle, Herbert; Janecke, Andreas R.; Kellner, Ulrich; Liskova, Petra; Lorenz, Birgit; Martorell-Sampol, Loreto; Messias, Andre; Meunier, Isabelle; Belga Ottoni Porto, Fernanda; Papageorgiou, Eleni; Plomp, Astrid S.; de Ravel, Thomy J. L.; Reiff, Charlotte M.; Renner, Agnes B.; Rosenberg, Thomas; Rudolph, Guenther; Salati, Roberto; Sener, E. Cumhur; Sieving, Paul A.; Stanzial, Franco; Traboulsi, Elias I.; Tsang, Stephen H.; Varsanyi, Balazs; Weleber, Richard G.; Zobor, Ditta; Stingl, Katarina; Wissinger, Bernd und Kohl, Susanne
(2022):
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.
In: Human Mutation, Bd. 43, Nr. 7: S. 832-858
Larsen, Petra P.; Thiele, Sarah; Krohne, Tim U.; Ziemssen, Focke; Krummenauer, Frank; Holz, Frank G.; Finger, Robert P.; Kohnen, Thomas; Naycheva, Lubka; Jochem, Maximilian; Reinhard, Thomas; Boehringer, Daniel; Engesser, Diana; Lagreze, Wolf; Müller, Claudia; Wolff, Carolin; Schmitz, Jessica; Lorenz, Birgit; Papadopoulou-Laiou, Chrysanthi; Holve, Kerstin; Schweinfurth, Silke; Hoerauf, Hans; Schwarz, Wiebke; Spitzer, Martin; Wagenfeld, Lars; Bertram, Paul; Auffarth, Gerd; Gavrilovic, Branka; Cursiefen, Claus; Schaub, Friederike; Lentzsch, Anna; Welsandt, Gerhard; Thieme, Hagen; Weigel, Melanie; Hidaya, Diyala; Ehmer, Angela; Priglinger, Siegfried; Livonius, Bettina von; Drexler, Carina; Semmelsberger, Jessica; Eter, Nicole; Alten, Florian; Sigleur, Annika; Sieber, Dorothee; Bräutigam, Andrea; Härter, Friederike; Adorf, Adeline; Pauleikhoff, Daniel; Robering, Angela; Helbig, Horst; Brandl, Caroline; Ziemssen, Focke; Roeck, Daniel; Krummenauer, Frank; Tulka, Sabrina; Wabbels, Bettina; Kupitz, David. G.; Göbel, Arno P.; Steinberg, Julia; Larsen, Petra P.; Schnetzer, Anne; Kobialka, Bianka; Prinz, Beate; Kutten, Danielle; Schneider, Pia; Toczko, Olivia und Yoganathan, Thanushiya
(2019):
Visual impairment and blindness in institutionalized elderly in Germany.
In: Graefes Archive for Clinical and Experimental Ophthalmology, Bd. 257, Nr. 2: S. 363-370
Michalakis, Stylianos; Shaltiel, Lior; Sothilingam, Vithiyanjali; Koch, Susanne; Schludi, Verena; Krause, Stefanie; Zeitz, Christina; Audo, Isabelle; Lancelot, Marie-Elise; Hamel, Christian; Meunier, Isabelle; Preising, Markus N.; Friedburg, Christoph; Lorenz, Birgit; Zabouri, Nawal; Haverkamp, Silke; Garcia Garrido, Marina; Tanimoto, Naoyuki; Seeliger, Mathias W.; Biel, Martin und Wahl-Schott, Christian A.
(2017):
Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2 (vol 23, pg 1538, 2014).
In: Human Molecular Genetics, Bd. 26, Nr. 2: S. 466