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David Birch

Showing results (31-40 of 43) with videos related to

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Ophthalmic Research|August 16, 2018
The Progression of the Stargardt Disease Type 4 (ProgStar-4) Study: Design and Baseline Characteristics (ProgStar-4 Report No. 1)Rupert W Strauss, Beatriz Muñoz, Mohamed I Ahmed, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Protocol for NAC Attack, a phase-3, multicenter randomized, parallel, double masked, placebo controlled trial evaluating the efficacy and safety of oral N-acetylcysteine (NAC) in patients with retinitis pigmentosaXiangrong Kong, Folahan Ibukun, Muhammad J Khan, et al.
American Journal of Human Genetics|May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosaDebra K Breuer, Beverly M Yashar, Elena Filippova, et al.
Human Genetics|January 31, 2016
Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trialNicola G Ghazi, Emad B Abboud, Sawsan R Nowilaty, et al.
Journal of Medical Genetics|July 13, 2013
Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencingXia Wang, Hui Wang, Vincent Sun, et al.
Scientific Reports|June 25, 2016
De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone MonochromacyElena Buena-Atienza, Klaus Rüther, Britta Baumann, et al.
Applied Spectroscopy|December 10, 2003
Aqueous solutions of uranium(VI) as studied by time-resolved emission spectroscopy: a round-robin testIsabelle Billard, Eric Ansoborlo, Kathleen Apperson, et al.
Investigative Ophthalmology & Visual Science|November 15, 2012
Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative diseaseKari Branham, Mohammad Othman, Matthew Brumm, et al.
Ophthalmology|July 26, 2016
Five-Year Safety and Performance Results from the Argus II Retinal Prosthesis System Clinical TrialLyndon da Cruz, Jessy D Dorn, Mark S Humayun, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2022
The landscape of submicroscopic structural variants at the <i>OPN1LW/OPN1MW</i> gene cluster on Xq28 underlying blue cone monochromacyBernd Wissinger, Britta Baumann, Elena Buena-Atienza, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Ophthalmic Research|August 16, 2018
The Progression of the Stargardt Disease Type 4 (ProgStar-4) Study: Design and Baseline Characteristics (ProgStar-4 Report No. 1)Rupert W Strauss, Beatriz Muñoz, Mohamed I Ahmed, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Protocol for NAC Attack, a phase-3, multicenter randomized, parallel, double masked, placebo controlled trial evaluating the efficacy and safety of oral N-acetylcysteine (NAC) in patients with retinitis pigmentosaXiangrong Kong, Folahan Ibukun, Muhammad J Khan, et al.
American Journal of Human Genetics|May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosaDebra K Breuer, Beverly M Yashar, Elena Filippova, et al.
Human Genetics|January 31, 2016
Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trialNicola G Ghazi, Emad B Abboud, Sawsan R Nowilaty, et al.
Journal of Medical Genetics|July 13, 2013
Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencingXia Wang, Hui Wang, Vincent Sun, et al.
Scientific Reports|June 25, 2016
De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone MonochromacyElena Buena-Atienza, Klaus Rüther, Britta Baumann, et al.
Applied Spectroscopy|December 10, 2003
Aqueous solutions of uranium(VI) as studied by time-resolved emission spectroscopy: a round-robin testIsabelle Billard, Eric Ansoborlo, Kathleen Apperson, et al.
Investigative Ophthalmology & Visual Science|November 15, 2012
Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative diseaseKari Branham, Mohammad Othman, Matthew Brumm, et al.
Ophthalmology|July 26, 2016
Five-Year Safety and Performance Results from the Argus II Retinal Prosthesis System Clinical TrialLyndon da Cruz, Jessy D Dorn, Mark S Humayun, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 27, 2022
The landscape of submicroscopic structural variants at the <i>OPN1LW/OPN1MW</i> gene cluster on Xq28 underlying blue cone monochromacyBernd Wissinger, Britta Baumann, Elena Buena-Atienza, et al.
Pageof 5