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Martin McKibbin

Showing results (61-70 of 106) with videos related to

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Investigative Ophthalmology & Visual Science|June 4, 2025
Expansion of the ABCA4-Associated Retinopathy Spectrum: Severe Variants Can be Associated With Early-Onset Severe Retinal DystrophyDaan M Panneman, Rebekkah J Hitti-Malin, Martin McKibbin, et al.
Eye (London, England)|April 23, 2024
Subretinal transient hyporeflectivity in neovascular age-related macular degeneration and its response to a loading phase of aflibercept: PRECISE report 4Andrea Montesel, Raheeba Pakeer Muhammed, Swati Chandak, et al.
American Journal of Ophthalmology|May 2, 2016
Defining a Minimum Set of Standardized Patient-centered Outcome Measures for Macular DegenerationIan A Rodrigues, Sara M Sprinkhuizen, Daniel Barthelmes, et al.
European Journal of Human Genetics : EJHG|February 3, 2018
A clinical and molecular characterisation of CRB1-associated maculopathyKamron N Khan, Anthony Robson, Omar A R Mahroo, et al.
Eye (London, England)|October 18, 2023
Associations of presenting visual acuity with morphological changes on OCT in neovascular age-related macular degeneration: PRECISE Study Report 2Shruti Chandra, Sarega Gurudas, Benjamin J L Burton, et al.
Investigative Ophthalmology & Visual Science|August 25, 2011
Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosaManir Ali, Paul M Hocking, Martin McKibbin, et al.
Stem Cell Reports|July 4, 2024
Retinal cells derived from patients with DRAM2-dependent CORD21 dystrophy exhibit key lysosomal enzyme deficiency and lysosomal content accumulationRozaliya Tsikandelova, Eldo Galo, Edvinas Cerniauskas, et al.
American Journal of Human Genetics|May 19, 2015
Biallelic mutations in the autophagy regulator DRAM2 cause retinal dystrophy with early macular involvementMohammed E El-Asrag, Panagiotis I Sergouniotis, Martin McKibbin, et al.
Human Mutation|May 7, 2019
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 geneJulia Felden, Britta Baumann, Manir Ali, et al.
Eye (London, England)|March 11, 2026
Real-world treatment patterns and visual outcomes of faricimab in patients with neovascular age-related macular degeneration in the UK at 12 months: the FARWIDE-nAMD studyJames Talks, Gabriella de Salvo, Praveen J Patel, et al.
Pageof 11

Showing results (61-70 of 106) with videos related to

Sort By:
Pageof 11
Investigative Ophthalmology & Visual Science|June 4, 2025
Expansion of the ABCA4-Associated Retinopathy Spectrum: Severe Variants Can be Associated With Early-Onset Severe Retinal DystrophyDaan M Panneman, Rebekkah J Hitti-Malin, Martin McKibbin, et al.
Eye (London, England)|April 23, 2024
Subretinal transient hyporeflectivity in neovascular age-related macular degeneration and its response to a loading phase of aflibercept: PRECISE report 4Andrea Montesel, Raheeba Pakeer Muhammed, Swati Chandak, et al.
American Journal of Ophthalmology|May 2, 2016
Defining a Minimum Set of Standardized Patient-centered Outcome Measures for Macular DegenerationIan A Rodrigues, Sara M Sprinkhuizen, Daniel Barthelmes, et al.
European Journal of Human Genetics : EJHG|February 3, 2018
A clinical and molecular characterisation of CRB1-associated maculopathyKamron N Khan, Anthony Robson, Omar A R Mahroo, et al.
Eye (London, England)|October 18, 2023
Associations of presenting visual acuity with morphological changes on OCT in neovascular age-related macular degeneration: PRECISE Study Report 2Shruti Chandra, Sarega Gurudas, Benjamin J L Burton, et al.
Investigative Ophthalmology & Visual Science|August 25, 2011
Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosaManir Ali, Paul M Hocking, Martin McKibbin, et al.
Stem Cell Reports|July 4, 2024
Retinal cells derived from patients with DRAM2-dependent CORD21 dystrophy exhibit key lysosomal enzyme deficiency and lysosomal content accumulationRozaliya Tsikandelova, Eldo Galo, Edvinas Cerniauskas, et al.
American Journal of Human Genetics|May 19, 2015
Biallelic mutations in the autophagy regulator DRAM2 cause retinal dystrophy with early macular involvementMohammed E El-Asrag, Panagiotis I Sergouniotis, Martin McKibbin, et al.
Human Mutation|May 7, 2019
Mutation spectrum and clinical investigation of achromatopsia patients with mutations in the GNAT2 geneJulia Felden, Britta Baumann, Manir Ali, et al.
Eye (London, England)|March 11, 2026
Real-world treatment patterns and visual outcomes of faricimab in patients with neovascular age-related macular degeneration in the UK at 12 months: the FARWIDE-nAMD studyJames Talks, Gabriella de Salvo, Praveen J Patel, et al.
Pageof 11