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Acta Ophthalmologica|November 29, 2014
Phenotype variations of retinal dystrophies caused by mutations in the RLBP1 geneStephanie Hipp, Gergely Zobor, Nicola Glöckle, et al.
Neuroimage|November 26, 2023
Targeting motor cortex high-excitability states defined by functional connectivity with real-time EEG-TMSDavid Emanuel Vetter, Christoph Zrenner, Paolo Belardinelli, et al.
Journal of Cardiovascular Electrophysiology|June 19, 2001
Dissociation between coronary sinus and left atrial conduction in patients with atrial fibrillation and flutterG Ndrepepa, B Zrenner, M A Schneider, et al.
Journal of Cardiovascular Electrophysiology|May 16, 2000
Noncontact mapping-guided catheter ablation of atrial fibrillation associated with left atrial ectopyM A Schneider, G Ndrepepa, B Zrenner, et al.
The British Journal of Ophthalmology|February 28, 2002
A novel mutation of the RP1 gene (Lys778ter) associated with autosomal dominant retinitis pigmentosaK Dietrich, F K Jacobi, S Tippmann, et al.
Annals of Neurology|October 1, 1993
Impairment of retinal increment thresholds in Huntington's diseaseW Paulus, G Schwarz, A Werner, et al.
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