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Jacque L Duncan

Showing results (131-140 of 170) with videos related to

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Physiological Genomics|January 29, 2017
Genetic analysis of 10 pedigrees with inherited retinal degeneration by exome sequencing and phenotype-genotype associationPooja Biswas, Jacque L Duncan, Bruno Maranhao, et al.
American Journal of Ophthalmology|December 22, 2023
Functional Vision in Patients With Biallelic USH2A VariantsElise Heon, Michele Melia, Laura E Bocchino, et al.
Research Square|February 26, 2024
Coding and non-coding variants in the ciliopathy gene <i>CFAP410</i> cause early-onset non-syndromic retinal degenerationRiccardo Sangermano, Priya Gupta, Cherrell Price, et al.
American Journal of Ophthalmology|February 10, 2023
Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 YearsJacque L Duncan, Peiyao Cheng, Maureen G Maguire, et al.
Clinical & Experimental Optometry|January 26, 2016
An analysis of observer-rated functional vision in patients implanted with the Argus II Retinal Prosthesis System at three yearsDuane R Geruschat, Thomas P Richards, Aries Arditi, et al.
American Journal of Medical Genetics. Part A|July 31, 2021
Auditory and olfactory findings in patients with USH2A-related retinal degeneration-Findings at baseline from the rate of progression in USH2A-related retinal degeneration natural history study (RUSH2A)Alessandro Iannaccone, Carmen C Brewer, Peiyao Cheng, et al.
Ophthalmology|January 17, 2012
Interim results from the international trial of Second Sight's visual prosthesisMark S Humayun, Jessy D Dorn, Lyndon da Cruz, et al.
NPJ Genomic Medicine|November 8, 2024
Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degenerationRiccardo Sangermano, Priya Gupta, Cherrell Price, et al.
The British Journal of Ophthalmology|May 24, 2014
The reliability of parafoveal cone density measurementsBenjamin S Liu, Sergey Tarima, Alexis Visotcky, et al.
Orphanet Journal of Rare Diseases|April 2, 2022
Expanding the phenotype of TTLL5-associated retinal dystrophy: a case seriesJin Kyun Oh, José G Vargas Del Valle, Jose Ronaldo Lima de Carvalho, et al.
Pageof 17

Showing results (131-140 of 170) with videos related to

Sort By:
Pageof 17
Physiological Genomics|January 29, 2017
Genetic analysis of 10 pedigrees with inherited retinal degeneration by exome sequencing and phenotype-genotype associationPooja Biswas, Jacque L Duncan, Bruno Maranhao, et al.
American Journal of Ophthalmology|December 22, 2023
Functional Vision in Patients With Biallelic USH2A VariantsElise Heon, Michele Melia, Laura E Bocchino, et al.
Research Square|February 26, 2024
Coding and non-coding variants in the ciliopathy gene <i>CFAP410</i> cause early-onset non-syndromic retinal degenerationRiccardo Sangermano, Priya Gupta, Cherrell Price, et al.
American Journal of Ophthalmology|February 10, 2023
Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 YearsJacque L Duncan, Peiyao Cheng, Maureen G Maguire, et al.
Clinical & Experimental Optometry|January 26, 2016
An analysis of observer-rated functional vision in patients implanted with the Argus II Retinal Prosthesis System at three yearsDuane R Geruschat, Thomas P Richards, Aries Arditi, et al.
American Journal of Medical Genetics. Part A|July 31, 2021
Auditory and olfactory findings in patients with USH2A-related retinal degeneration-Findings at baseline from the rate of progression in USH2A-related retinal degeneration natural history study (RUSH2A)Alessandro Iannaccone, Carmen C Brewer, Peiyao Cheng, et al.
Ophthalmology|January 17, 2012
Interim results from the international trial of Second Sight's visual prosthesisMark S Humayun, Jessy D Dorn, Lyndon da Cruz, et al.
NPJ Genomic Medicine|November 8, 2024
Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degenerationRiccardo Sangermano, Priya Gupta, Cherrell Price, et al.
The British Journal of Ophthalmology|May 24, 2014
The reliability of parafoveal cone density measurementsBenjamin S Liu, Sergey Tarima, Alexis Visotcky, et al.
Orphanet Journal of Rare Diseases|April 2, 2022
Expanding the phenotype of TTLL5-associated retinal dystrophy: a case seriesJin Kyun Oh, José G Vargas Del Valle, Jose Ronaldo Lima de Carvalho, et al.
Pageof 17