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Thales A C de Guimaraes

Showing results (1-10 of 19) with videos related to

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Retinal Cases & Brief Reports|March 4, 2024
SHWACHMAN-DIAMOND SYNDROME ASSOCIATED WITH ROD-CONE DYSTROPHYJingwen Zhang, Thales A C de Guimaraes, Dorothy Thompson, et al.
Translational Vision Science & Technology|May 6, 2025
Distance From the Foveal Center: A Method for the Calculation of Eccentric FixationThales A C de Guimaraes, Angelos Kalitzeos, James Bainbridge, et al.
Ophthalmic Genetics|May 23, 2020
<i>KCNV2</i> retinopathy: clinical features, molecular genetics and directions for future therapyThales A C De Guimaraes, Michalis Georgiou, Anthony G Robson, et al.
Translational Vision Science & Technology|April 9, 2024
In-Depth Retinal Sensitivity Assessment With the MP3 Type S Microperimeter: A Methods StudyThales A C de Guimaraes, Isabela M C de Guimaraes, Naser Ali, et al.
Investigative Ophthalmology & Visual Science|January 10, 2025
Retinal Sensitivity in KCNV2-Associated RetinopathyThales A C de Guimaraes, Isabela M C de Guimaraes, Manickam Nick Muthiah, et al.
Ophthalmic Genetics|March 8, 2024
Structural and functional characterization of an individual with the M285R <i>KCNV2</i> hypomorphic alleleThales A C de Guimaraes, Francesco Lai, Raffaella Colombatti, et al.
Ophthalmic Genetics|February 19, 2026
<i>CDH23</i>-associated Usher syndrome: genotype-phenotype correlationsThales A C de Guimaraes, Marcos Espinosa, Juan Carlos Romo-Aguas, et al.
American Journal of Ophthalmology|May 20, 2024
Clinical, Ophthalmic, and Genetic Characterization of RPGRIP1-Associated Leber Congenital Amaurosis/Early-Onset Severe Retinal DystrophyMalena Daich Varela, Mrunmayi Jeste, Thales A C de Guimaraes, et al.
Ophthalmology. Retina|March 24, 2024
Congenital Stationary Night Blindness: Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 PatientsMohamed Katta, Thales A C de Guimaraes, Yu Fujinami-Yokokawa, et al.
Ophthalmic Genetics|October 15, 2024
Bardet-Biedl syndrome with chorioretinal coloboma: a case series and review of literatureGoura Chattannavar, Marina Ger, Jeyapoorani Balasubramanian, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Retinal Cases & Brief Reports|March 4, 2024
SHWACHMAN-DIAMOND SYNDROME ASSOCIATED WITH ROD-CONE DYSTROPHYJingwen Zhang, Thales A C de Guimaraes, Dorothy Thompson, et al.
Translational Vision Science & Technology|May 6, 2025
Distance From the Foveal Center: A Method for the Calculation of Eccentric FixationThales A C de Guimaraes, Angelos Kalitzeos, James Bainbridge, et al.
Ophthalmic Genetics|May 23, 2020
<i>KCNV2</i> retinopathy: clinical features, molecular genetics and directions for future therapyThales A C De Guimaraes, Michalis Georgiou, Anthony G Robson, et al.
Translational Vision Science & Technology|April 9, 2024
In-Depth Retinal Sensitivity Assessment With the MP3 Type S Microperimeter: A Methods StudyThales A C de Guimaraes, Isabela M C de Guimaraes, Naser Ali, et al.
Investigative Ophthalmology & Visual Science|January 10, 2025
Retinal Sensitivity in KCNV2-Associated RetinopathyThales A C de Guimaraes, Isabela M C de Guimaraes, Manickam Nick Muthiah, et al.
Ophthalmic Genetics|March 8, 2024
Structural and functional characterization of an individual with the M285R <i>KCNV2</i> hypomorphic alleleThales A C de Guimaraes, Francesco Lai, Raffaella Colombatti, et al.
Ophthalmic Genetics|February 19, 2026
<i>CDH23</i>-associated Usher syndrome: genotype-phenotype correlationsThales A C de Guimaraes, Marcos Espinosa, Juan Carlos Romo-Aguas, et al.
American Journal of Ophthalmology|May 20, 2024
Clinical, Ophthalmic, and Genetic Characterization of RPGRIP1-Associated Leber Congenital Amaurosis/Early-Onset Severe Retinal DystrophyMalena Daich Varela, Mrunmayi Jeste, Thales A C de Guimaraes, et al.
Ophthalmology. Retina|March 24, 2024
Congenital Stationary Night Blindness: Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 PatientsMohamed Katta, Thales A C de Guimaraes, Yu Fujinami-Yokokawa, et al.
Ophthalmic Genetics|October 15, 2024
Bardet-Biedl syndrome with chorioretinal coloboma: a case series and review of literatureGoura Chattannavar, Marina Ger, Jeyapoorani Balasubramanian, et al.
Pageof 2