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Jacque L Duncan

Showing results (151-160 of 170) with videos related to

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American Journal of Ophthalmology|May 25, 2020
Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease SeverityJacque L Duncan, Wendi Liang, Maureen G Maguire, et al.
American Journal of Ophthalmology|March 29, 2025
Characterization of Visual Field Loss Over 4 Years in the Rate of Progression in USH2A-Related Retinal Degeneration (RUSH2A) StudyJacque L Duncan, Maureen G Maguire, Lee S McDaniel, et al.
Human Molecular Genetics|June 7, 2020
Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weaknessAnne Slavotinek, Doriana Misceo, Stephanie Htun, et al.
Investigative Ophthalmology & Visual Science|December 23, 2021
Comparative Natural History of Visual Function From Patients With Biallelic Variants in BBS1 and BBS10Monika K Grudzinska Pechhacker, Samuel G Jacobson, Arlene V Drack, et al.
Investigative Ophthalmology & Visual Science|June 4, 2024
Self-Reported Functional Vision in USH2A-Associated Retinal Degeneration as Measured by the Michigan Retinal Degeneration QuestionnaireBela Parekh, Jacque L Duncan, Lassana Samarakoon, et al.
Investigative Ophthalmology & Visual Science|February 5, 2025
Characterizing the Genetic Basis for Inherited Retinal Disease: Lessons Learned From the Foundation Fighting Blindness Clinical Consortium's Gene PollKari Branham, Lassana Samarakoon, Isabelle Audo, et al.
Translational Vision Science & Technology|October 9, 2024
Endpoints and Design for Clinical Trials in USH2A-Related Retinal Degeneration: Results and Recommendations From the RUSH2A Natural History StudyMaureen G Maguire, David G Birch, Jacque L Duncan, et al.
American Journal of Ophthalmology|August 25, 2022
Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation With Disease SeverityEleonora M Lad, Jacque L Duncan, Wendi Liang, et al.
JAMA Neurology|August 12, 2014
Effects of the absence of apolipoprotein e on lipoproteins, neurocognitive function, and retinal functionAngel C Y Mak, Clive R Pullinger, Ling Fung Tang, 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.
Pageof 17

Showing results (151-160 of 170) with videos related to

Sort By:
Pageof 17
American Journal of Ophthalmology|May 25, 2020
Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease SeverityJacque L Duncan, Wendi Liang, Maureen G Maguire, et al.
American Journal of Ophthalmology|March 29, 2025
Characterization of Visual Field Loss Over 4 Years in the Rate of Progression in USH2A-Related Retinal Degeneration (RUSH2A) StudyJacque L Duncan, Maureen G Maguire, Lee S McDaniel, et al.
Human Molecular Genetics|June 7, 2020
Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weaknessAnne Slavotinek, Doriana Misceo, Stephanie Htun, et al.
Investigative Ophthalmology & Visual Science|December 23, 2021
Comparative Natural History of Visual Function From Patients With Biallelic Variants in BBS1 and BBS10Monika K Grudzinska Pechhacker, Samuel G Jacobson, Arlene V Drack, et al.
Investigative Ophthalmology & Visual Science|June 4, 2024
Self-Reported Functional Vision in USH2A-Associated Retinal Degeneration as Measured by the Michigan Retinal Degeneration QuestionnaireBela Parekh, Jacque L Duncan, Lassana Samarakoon, et al.
Investigative Ophthalmology & Visual Science|February 5, 2025
Characterizing the Genetic Basis for Inherited Retinal Disease: Lessons Learned From the Foundation Fighting Blindness Clinical Consortium's Gene PollKari Branham, Lassana Samarakoon, Isabelle Audo, et al.
Translational Vision Science & Technology|October 9, 2024
Endpoints and Design for Clinical Trials in USH2A-Related Retinal Degeneration: Results and Recommendations From the RUSH2A Natural History StudyMaureen G Maguire, David G Birch, Jacque L Duncan, et al.
American Journal of Ophthalmology|August 25, 2022
Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation With Disease SeverityEleonora M Lad, Jacque L Duncan, Wendi Liang, et al.
JAMA Neurology|August 12, 2014
Effects of the absence of apolipoprotein e on lipoproteins, neurocognitive function, and retinal functionAngel C Y Mak, Clive R Pullinger, Ling Fung Tang, 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.
Pageof 17