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Winston Lee

Showing results (81-90 of 124) with videos related to

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Retinal Cases & Brief Reports|November 18, 2014
Jak2 mutation-positive polycythemia vera presenting as central retinal artery occlusionElona Dhrami-Gavazi, Winston Lee, Jason D Horowitz, et al.
American Journal of Ophthalmology Case Reports|August 5, 2024
A <i>GUCY2D</i> variant associated cone-rod dystrophy with electronegative ERG: A case report and reviewPei-Liang Wu, Pei-Hsuan Lin, Winston Lee, et al.
Scientific Reports|January 31, 2019
Hyperautofluorescent Dots are Characteristic in Ceramide Kinase Like-associated Retinal DegenerationJesse D Sengillo, Galaxy Y Cho, Maarjaliis Paavo, et al.
Investigative Ophthalmology & Visual Science|October 20, 2017
A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence in Stargardt DiseaseVivienne C Greenstein, Jason Nunez, Winston Lee, et al.
Investigative Ophthalmology & Visual Science|August 21, 2014
The external limiting membrane in early-onset Stargardt diseaseWinston Lee, Kalev Nõupuu, Maris Oll, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
Genotypic spectrum and phenotype correlations of ABCA4-associated disease in patients of south Asian descentWinston Lee, Kaspar Schuerch, Jana Zernant, et al.
Ophthalmic Genetics|October 3, 2019
Modification of the <i>PROM1</i> disease phenotype by a mutation in <i>ABCA4</i>Winston Lee, Maarjaliis Paavo, Jana Zernant, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 31, 2019
A case-control collapsing analysis identifies retinal dystrophy genes associated with ophthalmic disease in patients with no pathogenic ABCA4 variantsCharles J Wolock, Nicholas Stong, Chu Jian Ma, et al.
Translational Vision Science & Technology|May 1, 2023
Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus AutofluorescenceVivienne C Greenstein, David S Castillejos, Stephen H Tsang, et al.
American Journal of Ophthalmology|March 19, 2018
A Distinct Phenotype of Eyes Shut Homolog (EYS)-Retinitis Pigmentosa Is Associated With Variants Near the C-TerminusJesse D Sengillo, Winston Lee, Takayuki Nagasaki, et al.
Pageof 13

Showing results (81-90 of 124) with videos related to

Sort By:
Pageof 13
Retinal Cases & Brief Reports|November 18, 2014
Jak2 mutation-positive polycythemia vera presenting as central retinal artery occlusionElona Dhrami-Gavazi, Winston Lee, Jason D Horowitz, et al.
American Journal of Ophthalmology Case Reports|August 5, 2024
A <i>GUCY2D</i> variant associated cone-rod dystrophy with electronegative ERG: A case report and reviewPei-Liang Wu, Pei-Hsuan Lin, Winston Lee, et al.
Scientific Reports|January 31, 2019
Hyperautofluorescent Dots are Characteristic in Ceramide Kinase Like-associated Retinal DegenerationJesse D Sengillo, Galaxy Y Cho, Maarjaliis Paavo, et al.
Investigative Ophthalmology & Visual Science|October 20, 2017
A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence in Stargardt DiseaseVivienne C Greenstein, Jason Nunez, Winston Lee, et al.
Investigative Ophthalmology & Visual Science|August 21, 2014
The external limiting membrane in early-onset Stargardt diseaseWinston Lee, Kalev Nõupuu, Maris Oll, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
Genotypic spectrum and phenotype correlations of ABCA4-associated disease in patients of south Asian descentWinston Lee, Kaspar Schuerch, Jana Zernant, et al.
Ophthalmic Genetics|October 3, 2019
Modification of the <i>PROM1</i> disease phenotype by a mutation in <i>ABCA4</i>Winston Lee, Maarjaliis Paavo, Jana Zernant, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 31, 2019
A case-control collapsing analysis identifies retinal dystrophy genes associated with ophthalmic disease in patients with no pathogenic ABCA4 variantsCharles J Wolock, Nicholas Stong, Chu Jian Ma, et al.
Translational Vision Science & Technology|May 1, 2023
Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus AutofluorescenceVivienne C Greenstein, David S Castillejos, Stephen H Tsang, et al.
American Journal of Ophthalmology|March 19, 2018
A Distinct Phenotype of Eyes Shut Homolog (EYS)-Retinitis Pigmentosa Is Associated With Variants Near the C-TerminusJesse D Sengillo, Winston Lee, Takayuki Nagasaki, et al.
Pageof 13