Quasi-Monopolar Stimulation: A Novel Electrode Design Configuration for Performance Optimization of a Retinal Neuroprosthesis

Por Khalili Moghadam, Gita, Wilke, Robert, Suaning, Gregg J., Lovell, Nigel H., Dokos, Socrates
Publicado em 2013

Structure-Function Correlation of the Human Central Retina

Por Charbel Issa, Peter, Troeger, Eric, Finger, Robert, Holz, Frank G., Wilke, Robert, Scholl, Hendrik P. N.
Publicado em 2010

Mutation Analysis Identifies GUCY2D as the Major Gene Responsible for Autosomal Dominant Progressive Cone Degeneration

Por Kitiratschky, Veronique B. D., Wilke, Robert, Renner, Agnes B., Kellner, Ulrich, Vadalà, Maria, Birch, David G., Wissinger, Bernd, Zrenner, Eberhart, Kohl, Susanne
Publicado no Invest Ophthalmol Vis Sci (2008)

Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy

Por Wycisk, Katharina Agnes, Zeitz, Christina, Feil, Silke, Wittmer, Mariana, Forster, Ursula, Neidhardt, John, Wissinger, Bernd, Zrenner, Eberhart, Wilke, Robert, Kohl, Susanne, Berger, Wolfgang
Publicado em 2006

Molecular analysis of ABCA4 and CRB1 genes in a Spanish family segregating both Stargardt disease and autosomal recessive retinitis pigmentosa

Por Riveiro-Alvarez, Rosa, Vallespin, Elena, Wilke, Robert, Garcia-Sandoval, Blanca, Cantalapiedra, Diego, Aguirre-Lamban, Jana, Avila-Fernandez, Almudena, Gimenez, Ascension, Trujillo-Tiebas, Maria-Jose, Ayuso, Carmen
Publicado em 2008

Subretinal electronic chips allow blind patients to read letters and combine them to words

Por Zrenner, Eberhart, Bartz-Schmidt, Karl Ulrich, Benav, Heval, Besch, Dorothea, Bruckmann, Anna, Gabel, Veit-Peter, Gekeler, Florian, Greppmaier, Udo, Harscher, Alex, Kibbel, Steffen, Koch, Johannes, Kusnyerik, Akos, Peters, Tobias, Stingl, Katarina, Sachs, Helmut, Stett, Alfred, Szurman, Peter, Wilhelm, Barbara, Wilke, Robert
Publicado em 2011