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 
2 of 8 
2 of 8
- Fundus-Controlled Dark Adaptometry in Young Children Without and With Spontaneously Regressed Retinopathy of Prematurity (2019)
Bowl, Wadim; Lorenz, Birgit; Stieger, Knut; et al. - High-dose Anderson operation for nystagmus-related anomalous head turn (2019)
Graef, Michael; Hausmann, Anja; Lorenz, Birgit - Splitting of the lateral rectus muscle with medial transposition to treat oculomotor palsy: a retrospective analysis of 29 consecutive cases (2019)
Basiakos, Sotirios; Graef, Michael; Preising, Markus N.; et al. - The Natural History of Inherited Retinal Dystrophy Due to Biallelic Mutations in the RPE65 Gene (2019)
Chung, Daniel C.; Bertelsen, Mette; Lorenz, Birgit; et al. - The Phenotypic Spectrum of Ophthalmic Changes in CEP290 Mutations (2019)
Preising, Markus N.; Schneider, Ute; Friedburg, Christoph; et al. - Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders (2019)
Zeitz, Christina; Michiels, Christelle; Neuille, Marion; et al. - Choroidal Thickness with Swept-Source Optical Coherence Tomography versus Foveal Morphology in Young Children with a History of Prematurity (2018)
Bowl, Wadim; Bowl, Marianne; Schweinfurth, Silke; et al. - Unexpected Genetic Cause in Two Female Siblings with High Myopia and Reduced Visual Acuity (2018)
Preising, M. N.; Friedburg, C. F.; Bowl, W.; et al. - Genotype-Phenotype Correlations in Patients with CRB1 Mutations (2017)
Laiou, C. Papadopoulou; Preising, M. N.; Bolz, H. J.; et al. - Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2 (vol 23, pg 1538, 2014) (2017)
Michalakis, Stylianos; Shaltiel, Lior; Sothilingam, Vithiyanjali; et al.
