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Pacing and Clinical Electrophysiology : PACE|February 25, 1998
Intraoperative recordings of monophasic action potentials with chronically implantable pacemaker leadsB Zrenner, D Müssig, J Schreieck, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1991
Mizuo phenomenon in X-linked retinoschisis. Pathogenesis of the Mizuo phenomenonP T de Jong, E Zrenner, G J van Meel, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 24, 2015
Ophthalmological assessment of cannabis-induced persisting perception disorder: is there a direct retinal effect?Ditta Zobor, Torsten Strasser, Gergely Zobor, et al.
Journal of Medical Genetics|August 1, 1997
RDS/peripherin gene mutations are frequent causes of central retinal dystrophiesS Kohl, M Christ-Adler, E Apfelstedt-Sylla, et al.
Pacing and Clinical Electrophysiology : PACE|November 25, 1998
Internal cardioversion of atrial fibrillation with a single lead configuration in a patient with massive diaphragmatic herniationM A Schneider, S Weyerbrock, R Herrman, et al.
Ophthalmic Research|April 3, 2015
Ketogenic diet attenuates NMDA-induced damage to rat's retinal ganglion cells in an age-dependent mannerTomasz Zarnowski, Tomasz J Choragiewicz, Frank Schuettauf, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathyF K Jacobi, B Leo-Kottler, K Mittelviefhaus, et al.
Vision Research|March 1, 2014
Attenuation of S-cone function at high altitude assessed by electroretinographyAndreas Schatz, M Dominik Fischer, Kai Schommer, et al.
Neuroimage|November 7, 2021
Recording brain responses to TMS of primary motor cortex by EEG - utility of an optimized sham procedurePedro C Gordon, D Blair Jovellar, YuFei Song, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 25, 2002
Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX geneFelix K Jacobi, Sten Andréasson, Hana Langrova, et al.
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