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Gavin Arno

Showing results (61-70 of 185) with videos related to

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JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
Ophthalmology|November 18, 2022
ReplyChris F Inglehearn, Samar Yahya, Claire E L Smith, et al.
American Journal of Ophthalmology|November 10, 2019
GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel TherapiesZaina Bouzia, Michalis Georgiou, Sarah Hull, et al.
Cells|August 9, 2024
Investigating Splice Defects in <i>USH2A</i> Using Targeted Long-Read SequencingShwetha Chandrasekhar, Siying Lin, Neringa Jurkute, et al.
American Journal of Ophthalmology|July 8, 2023
Detailed Clinical, Ophthalmic, and Genetic Characterization of ADGRV1-Associated Usher SyndromeMalena Daich Varela, Shiao Wei Wong, Gulunay Kiray, et al.
Investigative Ophthalmology & Visual Science|March 11, 2026
Characterizing a Unique Retinal Phenotype in INTS11-Associated Neurodevelopmental DisorderSiying Lin, Wendy D Tan, Anthony G Robson, et al.
JAMA Ophthalmology|July 9, 2016
Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular DystrophySarah Hull, Gavin Arno, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|December 14, 2021
SSBP1-Disease Update: Expanding the Genetic and Clinical Spectrum, Reporting Variable Penetrance and Confirming Recessive InheritanceNeringa Jurkute, Fabiana D'Esposito, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|June 6, 2025
Clinical and Biochemical Characterization of Specific GUCY2D Alleles Associated With a Rare Form of Night BlindnessRola Ba-Abbad, Igor V Peshenko, Malena Daich Varela, et al.
Progress in Retinal and Eye Research|August 30, 2020
The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapiesSamantha R De Silva, Gavin Arno, Anthony G Robson, et al.
Pageof 19

Showing results (61-70 of 185) with videos related to

Sort By:
Pageof 19
JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
Ophthalmology|November 18, 2022
ReplyChris F Inglehearn, Samar Yahya, Claire E L Smith, et al.
American Journal of Ophthalmology|November 10, 2019
GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel TherapiesZaina Bouzia, Michalis Georgiou, Sarah Hull, et al.
Cells|August 9, 2024
Investigating Splice Defects in <i>USH2A</i> Using Targeted Long-Read SequencingShwetha Chandrasekhar, Siying Lin, Neringa Jurkute, et al.
American Journal of Ophthalmology|July 8, 2023
Detailed Clinical, Ophthalmic, and Genetic Characterization of ADGRV1-Associated Usher SyndromeMalena Daich Varela, Shiao Wei Wong, Gulunay Kiray, et al.
Investigative Ophthalmology & Visual Science|March 11, 2026
Characterizing a Unique Retinal Phenotype in INTS11-Associated Neurodevelopmental DisorderSiying Lin, Wendy D Tan, Anthony G Robson, et al.
JAMA Ophthalmology|July 9, 2016
Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular DystrophySarah Hull, Gavin Arno, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|December 14, 2021
SSBP1-Disease Update: Expanding the Genetic and Clinical Spectrum, Reporting Variable Penetrance and Confirming Recessive InheritanceNeringa Jurkute, Fabiana D'Esposito, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|June 6, 2025
Clinical and Biochemical Characterization of Specific GUCY2D Alleles Associated With a Rare Form of Night BlindnessRola Ba-Abbad, Igor V Peshenko, Malena Daich Varela, et al.
Progress in Retinal and Eye Research|August 30, 2020
The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapiesSamantha R De Silva, Gavin Arno, Anthony G Robson, et al.
Pageof 19