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Publications

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Filters: Keyword is Electroretinography  [Clear All Filters]
2022
Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series., Oh, Jin Kyun, Del Valle José G. Vargas, de Carvalho Jose Ronaldo Li, Sun Young Joo, Levi Sarah R., Ryu Joseph, Yang Jing, Nagasaki Takayuki, Emanuelli Andres, Rasool Nailyn, et al. , Orphanet J Rare Dis, 2022 04 01, Volume 17, Issue 1, p.146, (2022)
2016
CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa., Wu, Wen-Hsuan, Tsai Yi-Ting, Justus Sally, Lee Ting-Ting, Zhang Lijuan, Lin Chyuan-Sheng, Bassuk Alexander G., Mahajan Vinit B., and Tsang Stephen H. , Mol Ther, 2016 08, Volume 24, Issue 8, p.1388-94, (2016)
2010
Patients with an acute zonal occult outer retinopathy-like illness rapidly improve with valacyclovir treatment., Mahajan, Vinit B., and Stone Edwin M. , American journal of ophthalmology, 2010 Oct, Volume 150, Issue 4, p.511-8, (2010)
2009
A new macular dystrophy with anomalous vascular development, pigment spots, cystic spaces, and neovascularization., Mahajan, Vinit B., Russell Stephen R., and Stone Edwin M. , Archives of ophthalmology, 2009 Nov, Volume 127, Issue 11, p.1449-57, (2009)
2007
Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness., Tsang, Stephen H., Woodruff Michael L., Jun Lin, Mahajan Vinit, Yamashita Clyde K., Pedersen Robert, Lin Chyuan-Sheng, Goff Stephen P., Rosenberg Thomas, Larsen Michael, et al. , Human mutation, 2007 Mar, Volume 28, Issue 3, p.243-54, (2007)