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Vinit B Mahajan

Showing results (171-180 of 259) with videos related to

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Ophthalmic Surgery, Lasers & Imaging : the Official Journal of the International Society for Imaging in the Eye|August 2, 2011
Uveitis following intravitreal bevacizumab: a non-infectious clusterChristine N Kay, Ryan M Tarantola, Karen M Gehrs, et al.
Journal of Proteome Research|January 3, 2024
Liquid Biopsy Proteomics in OphthalmologyJulian Wolf, Joel A Franco, Rui Yip, et al.
Journal of Visualized Experiments : Jove|November 21, 2017
Dissection of Human Retina and RPE-Choroid for Proteomic AnalysisThiago Cabral, Marcus A Toral, Gabriel Velez, et al.
Ophthalmic Surgery, Lasers & Imaging Retina|May 21, 2026
A Simplified Classification for Age-Related Macular Degeneration Based on Optical Coherence TomographyTsai-Chu Yeh, Jonathan B Lin, Prithvi Mruthyunjaya, et al.
Cold Spring Harbor Molecular Case Studies|February 24, 2018
A novel de novo <i>CAPN5</i> mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delayGabriel Velez, Alexander G Bassuk, Kellie A Schaefer, et al.
Case Reports in Ophthalmology|January 22, 2015
Incomplete vitreomacular traction release using intravitreal ocriplasminEric K Chin, David R P Almeida, Elliott H Sohn, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 21, 2016
CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis PigmentosaWen-Hsuan Wu, Yi-Ting Tsai, Sally Justus, et al.
Ophthalmology|May 30, 2013
Combination therapy for neovascular age-related macular degeneration refractory to anti-vascular endothelial growth factor agentsKevin Tozer, A Brock Roller, Lawrence P Chong, et al.
Scientific Reports|September 6, 2017
Retrospective Analysis of Structural Disease Progression in Retinitis Pigmentosa Utilizing Multimodal ImagingThiago Cabral, Jesse D Sengillo, Jimmy K Duong, et al.
Orphanet Journal of Rare Diseases|August 17, 2018
Missense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesityKatherine Y Liu, Jesse D Sengillo, Gabriel Velez, et al.
Pageof 26

Showing results (171-180 of 259) with videos related to

Sort By:
Pageof 26
Ophthalmic Surgery, Lasers & Imaging : the Official Journal of the International Society for Imaging in the Eye|August 2, 2011
Uveitis following intravitreal bevacizumab: a non-infectious clusterChristine N Kay, Ryan M Tarantola, Karen M Gehrs, et al.
Journal of Proteome Research|January 3, 2024
Liquid Biopsy Proteomics in OphthalmologyJulian Wolf, Joel A Franco, Rui Yip, et al.
Journal of Visualized Experiments : Jove|November 21, 2017
Dissection of Human Retina and RPE-Choroid for Proteomic AnalysisThiago Cabral, Marcus A Toral, Gabriel Velez, et al.
Ophthalmic Surgery, Lasers & Imaging Retina|May 21, 2026
A Simplified Classification for Age-Related Macular Degeneration Based on Optical Coherence TomographyTsai-Chu Yeh, Jonathan B Lin, Prithvi Mruthyunjaya, et al.
Cold Spring Harbor Molecular Case Studies|February 24, 2018
A novel de novo <i>CAPN5</i> mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delayGabriel Velez, Alexander G Bassuk, Kellie A Schaefer, et al.
Case Reports in Ophthalmology|January 22, 2015
Incomplete vitreomacular traction release using intravitreal ocriplasminEric K Chin, David R P Almeida, Elliott H Sohn, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 21, 2016
CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis PigmentosaWen-Hsuan Wu, Yi-Ting Tsai, Sally Justus, et al.
Ophthalmology|May 30, 2013
Combination therapy for neovascular age-related macular degeneration refractory to anti-vascular endothelial growth factor agentsKevin Tozer, A Brock Roller, Lawrence P Chong, et al.
Scientific Reports|September 6, 2017
Retrospective Analysis of Structural Disease Progression in Retinitis Pigmentosa Utilizing Multimodal ImagingThiago Cabral, Jesse D Sengillo, Jimmy K Duong, et al.
Orphanet Journal of Rare Diseases|August 17, 2018
Missense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesityKatherine Y Liu, Jesse D Sengillo, Gabriel Velez, et al.
Pageof 26