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Peter Charbel Issa

Showing results (181-190 of 231) with videos related to

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Klinische Monatsblatter Fur Augenheilkunde|May 6, 2025
[Correction: N-Acetylcysteine (NAC) for Retinitis pigmentosa]Kristina Pfau, Josep Callizo, Petra Rossouw, et al.
American Journal of Ophthalmology|June 15, 2019
Improved Diagnosis of Retinal Laser Injuries Using Near-Infrared AutofluorescenceSamantha R De Silva, James E Neffendorf, Johannes Birtel, et al.
Investigative Ophthalmology & Visual Science|September 19, 2019
Binocular Inhibition of Reading in Macular Telangiectasia Type 2Simone Tzaridis, Philipp Herrmann, Peter Charbel Issa, et al.
Investigative Ophthalmology & Visual Science|August 9, 2017
Novel Insights Into the Phenotypical Spectrum of KIF11-Associated Retinopathy, Including a New Form of Retinal CiliopathyJohannes Birtel, Martin Gliem, Elisabeth Mangold, et al.
Investigative Ophthalmology & Visual Science|August 7, 2019
A Specific Macula-Predominant Retinal Phenotype Is Associated With the CDHR1 Variant c.783G>A, a Silent Mutation Leading to In-Frame Exon SkippingPeter Charbel Issa, Martin Gliem, Imran H Yusuf, et al.
Ophthalmic Research|January 2, 2023
Current Management of Inherited Retinal Degeneration Patients in Europe: Results of a 2-Year Follow-Up Multinational Survey by the European Vision Institute Clinical Research Network - EVICR.netBirgit Lorenz, Joana Tavares, L Ingeborgh van den Born, et al.
JAMA Network Open|February 9, 2019
Estimating Retinal Sensitivity Using Optical Coherence Tomography With Deep-Learning Algorithms in Macular Telangiectasia Type 2Yuka Kihara, Tjebo F C Heeren, Cecilia S Lee, et al.
Investigative Ophthalmology & Visual Science|June 28, 2011
Characterization of a dominant cone degeneration in a green fluorescent protein-reporter mouse with disruption of Loci associated with human dominant retinal dystrophyDaniel M Lipinski, Mohammed Yusuf, Alun R Barnard, et al.
Ophthalmic Research|March 6, 2023
Current Management of Patients with RPE65 Mutation Associated Inherited Retinal Degenerations in Europe: Results of a 2-Year Follow-Up Multinational SurveyBirgit Lorenz, Joana Tavares, L Ingeborgh van den Born, et al.
Retina (Philadelphia, Pa.)|May 26, 2017
LONGITUDINAL CORRELATION OF ELLIPSOID ZONE LOSS AND FUNCTIONAL LOSS IN MACULAR TELANGIECTASIA TYPE 2Tjebo F C Heeren, Diána Kitka, Daniela Florea, et al.
Pageof 24

Showing results (181-190 of 231) with videos related to

Sort By:
Pageof 24
Klinische Monatsblatter Fur Augenheilkunde|May 6, 2025
[Correction: N-Acetylcysteine (NAC) for Retinitis pigmentosa]Kristina Pfau, Josep Callizo, Petra Rossouw, et al.
American Journal of Ophthalmology|June 15, 2019
Improved Diagnosis of Retinal Laser Injuries Using Near-Infrared AutofluorescenceSamantha R De Silva, James E Neffendorf, Johannes Birtel, et al.
Investigative Ophthalmology & Visual Science|September 19, 2019
Binocular Inhibition of Reading in Macular Telangiectasia Type 2Simone Tzaridis, Philipp Herrmann, Peter Charbel Issa, et al.
Investigative Ophthalmology & Visual Science|August 9, 2017
Novel Insights Into the Phenotypical Spectrum of KIF11-Associated Retinopathy, Including a New Form of Retinal CiliopathyJohannes Birtel, Martin Gliem, Elisabeth Mangold, et al.
Investigative Ophthalmology & Visual Science|August 7, 2019
A Specific Macula-Predominant Retinal Phenotype Is Associated With the CDHR1 Variant c.783G>A, a Silent Mutation Leading to In-Frame Exon SkippingPeter Charbel Issa, Martin Gliem, Imran H Yusuf, et al.
Ophthalmic Research|January 2, 2023
Current Management of Inherited Retinal Degeneration Patients in Europe: Results of a 2-Year Follow-Up Multinational Survey by the European Vision Institute Clinical Research Network - EVICR.netBirgit Lorenz, Joana Tavares, L Ingeborgh van den Born, et al.
JAMA Network Open|February 9, 2019
Estimating Retinal Sensitivity Using Optical Coherence Tomography With Deep-Learning Algorithms in Macular Telangiectasia Type 2Yuka Kihara, Tjebo F C Heeren, Cecilia S Lee, et al.
Investigative Ophthalmology & Visual Science|June 28, 2011
Characterization of a dominant cone degeneration in a green fluorescent protein-reporter mouse with disruption of Loci associated with human dominant retinal dystrophyDaniel M Lipinski, Mohammed Yusuf, Alun R Barnard, et al.
Ophthalmic Research|March 6, 2023
Current Management of Patients with RPE65 Mutation Associated Inherited Retinal Degenerations in Europe: Results of a 2-Year Follow-Up Multinational SurveyBirgit Lorenz, Joana Tavares, L Ingeborgh van den Born, et al.
Retina (Philadelphia, Pa.)|May 26, 2017
LONGITUDINAL CORRELATION OF ELLIPSOID ZONE LOSS AND FUNCTIONAL LOSS IN MACULAR TELANGIECTASIA TYPE 2Tjebo F C Heeren, Diána Kitka, Daniela Florea, et al.
Pageof 24