Lorenz, Birgit
7 papers on CoChatORCID 0000-0002-9737-8127
Most cited papers
- Verified
Retinal layer segmentation in multiple sclerosis: a systematic review and meta-analysis
Petzold, A., Balcer, L. J., Calabresi, P. A., Costello, F., Frohman, T. C., Frohman, E. M., Martinez-Lapiscina, E. H., Green, A. J., Kardon, R., Outteryck, O., et al. (2017) · The Lancet Neurology
Multiple Sclerosis Research StudiesGlaucoma and retinal disorders
Cited by 585
- Verified
Positional cloning of the gene associated with X-linked juvenile retinoschisis
Sauer, C. G., Gehrig, A., Warneke-Wittstock, R., Marquardt, A., Ewing, C. C., Gibson, A., Lorenz, B., Jurklies, B., & Weber, B. H. F. (1997) · Nature Genetics
Retinal Development and DisordersOcular Disorders and Treatments
Cited by 497
- Verified
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. (2004) · Ophthalmology
Retinal Development and DisordersRetinal Diseases and Treatments
Cited by 172
- Verified
Detection of intact rAAV particles up to 6 years after successful gene transfer in the retina of dogs and primates
Stieger, K., Schroeder, J., Provost, N., Mendes-Madeira, A., Belbellaa, B., Meur, G. L., Weber, M., Deschamps, J.-Y., Lorenz, B., Moullier, P., et al. (2009) · Molecular Therapy
Virus-based gene therapy researchRetinal Development and Disorders
Cited by 88
- Verified
LACK OF AUTOFLUORESCENCE IN FUNDUS ALBIPUNCTATUS ASSOCIATED WITH MUTATIONS IN RDH5
Schatz, P., Preising, M., Lorenz, B., Sander, B., Larsen, M., Eckstein, C., & Rosenberg, T. (2010) · Retina
Retinal Development and DisordersRetinal Diseases and Treatments
Cited by 44
- Verified
Evaluation of tolerance to lentiviral LV-RPE65 gene therapy vector after subretinal delivery in non-human primates.
Matet, A., Kostic, C., Bemelmans, A.-P., Moulin, A., Rosolen, S. G., Martin, S., Mavilio, F., Amirjanians, V., Stieger, K., Lorenz, B., et al. (2017) · Translational Research
Retinal Development and DisordersVirus-based gene therapy research
Cited by 20
- Verified · note
Genetische und klinische Heterogenität bei LCA-Patienten: Das Ende der Einheitlichkeit
Preising, M. N., Paunescu, K., Friedburg, C., & Lorenz, B. (2007) · Der Ophthalmologe
Retinal Development and DisordersRetinal Diseases and Treatments
Cited by 17
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