Birgit Lorenz
Department of Pediatric Ophthalmology and Ophthalmic Genetics
Klinikum
University of Regensburg
Regensburg
Germany
Name/email consistency: high
- Ependymal tissue in microphthalmia with cyst. Lorenz, B., Elflein, H.M., Hofstädter, F. Ophthalmic Genet. (2006)
- Pediatric ophthalmology in Germany. Lorenz, B., Lenk-Schaefer, M. J. AAPOS (2006)
- Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65. Lorenz, B., Wabbels, B., Wegscheider, E., Hamel, C.P., Drexler, W., Preising, M.N. Ophthalmology (2004)
- Phenotype in two families with RP3 associated with RPGR mutations. Lorenz, B., Andrassi, M., Kretschmann, U. Ophthalmic Genet. (2003)
- First evidence of an endogenous Spiroplasma sp. infection in humans manifesting as unilateral cataract associated with anterior uveitis in a premature baby. Lorenz, B., Schroeder, J., Reischl, U. Graefes Arch. Clin. Exp. Ophthalmol. (2002)
- Early-onset severe rod-cone dystrophy in young children with RPE65 mutations. Lorenz, B., Gyürüs, P., Preising, M., Bremser, D., Gu, S., Andrassi, M., Gerth, C., Gal, A. Invest. Ophthalmol. Vis. Sci. (2000)
- Telemedicine based screening of infants at risk for retinopathy of prematurity. Lorenz, B., Bock, M., Müller, H.M., Massie, N.A. Stud. Health. Technol. Inform (1999)
