Zentrum für Augenheilkunde
Präsidium der Justus-Liebig-Universität Gießen » Fachbereiche » Fachbereich 11 - Humanmedizin » Dekanat Fachbereich 11 - Humanmedizin
Type of organisation: Institute
Subordinate Organisational Units
Publications 
21 of 28 
21 of 28
- 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. - Comparison of Central Retinal Thickness in Healthy Children and Adults Measured with the Heidelberg Spectralis OCT and the Zeiss Stratus OCT 3 (2011)
Chopovska, Yaroslava; Jaeger, Melanie; Rambow, Ronny; et al. - Fundus Albipunctatus Associated with Compound Heterozygous Mutations in RPE65 (2011)
Schatz, Patrik; Preising, Markus; Lorenz, Birgit; et al. - Interchangeability of macular thickness measurements between different volumetric protocols of Spectralis optical coherence tomography in normal eyes (2011)
Wenner, Yaroslava; Wismann, Stephan; Jaeger, Melanie; 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. - Long-Term Follow-Up of the Human Phenotype in Three Siblings with Cone Dystrophy Associated with a Homozygous p.G461R Mutation of KCNV2 (2011)
Friedburg, Christoph; Wissinger, Bernd; Schambeck, Maria; et al. - RPGR: Role in the photoreceptor cilium, human retinal disease, and gene therapy (2011)
Hosch, Jutta; Lorenz, Birgit; Stieger, Knut - Screening of TYR, OCA2, GPR143, and MC1R in patients with congenital nystagmus, macular hypoplasia, and fundus hypopigmentation indicating albinism (2011)
Preising, Markus N.; Forster, Hedwig; Gonser, Miriam; et al.
