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Journal of Vision|January 29, 2016
M-sequences in ophthalmic electrophysiologyPhilipp L Müller, Thomas Meigen
Zeitschrift Fur Medizinische Physik|June 7, 2007
[Adaptive estimation of contrast thresholds using the visual evoked potential (VEP)]Thomas Meigen, Franziska Kley
Vision Research|April 6, 2007
Optimizing electrode positions and analysis strategies for multifocal VEP recordings by ROC analysisThomas Meigen, Mathias Krämer
Documenta Ophthalmologica. Advances in Ophthalmology|April 24, 2004
The dependency of simultaneously recorded retinal and cortical potentials on temporal frequencyMonika Heine, Thomas Meigen
Retina (Philadelphia, Pa.)|October 6, 2010
Intravitreous injection of bevacizumab, tissue plasminogen activator, and gas in the treatment of submacular hemorrhage in age-related macular degenerationRainer Guthoff, Tanja Guthoff, Thomas Meigen, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|September 10, 2009
Comparison of bevacizumab and triamcinolone for treatment of macular edema secondary to central retinal vein occlusion--a matched-pairs analysisRainer Guthoff, Thomas Meigen, Kathrin Hennemann, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|April 29, 2010
Comparison of bevacizumab and triamcinolone for treatment of macular edema secondary to branch retinal vein occlusion in a pair-matched analysisRainer Guthoff, Thomas Meigen, Kathrin Hennemann, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 13, 2006
Clinical findings in a multigeneration family with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/RDS geneClaudia N Keilhauer, Thomas Meigen, Bernhard H F Weber
The British Journal of Ophthalmology|April 30, 2020
Retinal light sensitivity as outcome measure in recessive Stargardt diseaseMaximilian Pfau, Frank G Holz, Philipp L Müller
Ophthalmic Genetics|December 7, 2006
Late-onset central areolar choroidal dystrophy caused by a heterozygous frame-shift mutation affecting codon 307 of the peripherin/RDS geneClaudia N Keilhauer, Thomas Meigen, Heidi Stöhr, et al.
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