Zentrum für Augenheilkunde
Präsidium der Justus-Liebig-Universität Gießen » Fachbereiche » Fachbereich 11 - Humanmedizin » Dekanat Fachbereich 11 - Humanmedizin
Organisationstyp: Institut
Untergeordnete Organisationseinheit
Publikationen 
6 von 8 
6 von 8
- Autosomal Recessive Bestrophinopathy (ARB): A Clinical and Molecular Description of Two Patients at Childhood (2012)
Preising, M. N.; Pasquay, C.; Friedburg, C.; et al. - Bilateral Medial Rectus Recession with Posterior Fixation Suture for Large Infantile Esotropia (2012)
Graef, M.; Gerlach, T.; Borchert, O.; et al. - Chromatic Pupillometry Dissects Function of the Three Different Light-Sensitive Retinal Cell Populations in RPE65 Deficiency (2012)
Lorenz, Birgit; Strohmayr, Elisabeth; Zahn, Steffen; et al. - Mutations in RD3 Are Associated with an Extremely Rare and Severe Form of Early Onset Retinal Dystrophy (2012)
Preising, Markus N.; Hausotter-Will, Nora; Solbach, Manuel C.; et al. - Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness (2012)
Audo, Isabelle; Bujakowska, Kinga; Orhan, Elise; et al. - Autosomal Recessive Bestrophinopathy: New Observations on the Retinal Phenotype - Clinical and Molecular Report of an Italian Family (2011)
Guerriero, S.; Preising, M. N.; Ciccolella, N.; et al. - Blind spot enlargement syndrome in acute zonal occult outer retinopathy with detection of autoantibodies against the retinal antigens CRALBP and S-Ag (2011)
Neutzner, R. V.; Jaeger, M.; Friedburg, C.; et al. - Fundus Albipunctatus Associated with Compound Heterozygous Mutations in RPE65 (2011)
Schatz, Patrik; Preising, Markus; Lorenz, Birgit; et al. - Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response (2011)
Wissinger, Bernd; Schaich, Simone; Baumann, Britta; et al.
