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Rando Allikmets

Showing results (71-80 of 180) with videos related to

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Scientific Reports|April 25, 2019
Multi-platform imaging in ABCA4-Associated DiseaseLijuan Chen, Winston Lee, Jose Ronaldo Lima de Carvalho, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 23, 2013
Disruption of the human cone photoreceptor mosaic from a defect in NR2E3 transcription factor function in young adultsSung Pyo Park, In Hwan Hong, Stephen H Tsang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 14, 2009
Phenotypic features of patients with NR2E3 mutationsSophia I Pachydaki, Carolyn C Klaver, Irene A Barbazetto, et al.
Ophthalmic Genetics|November 9, 2011
Disruption in Bruch membrane in patients with Stargardt diseaseSung Pyo Park, Stanley Chang, Rando Allikmets, et al.
Investigative Ophthalmology & Visual Science|July 31, 2014
Choroidal and retinal thickening in severe preeclampsiaAakriti Garg, Ronald J Wapner, Cande V Ananth, et al.
Investigative Ophthalmology & Visual Science|January 31, 2002
Genotype-phenotype analysis of ABCR variants in macular degeneration probands and siblingsPaul S Bernstein, Mark Leppert, Nanda Singh, et al.
Investigative Ophthalmology & Visual Science|May 30, 2015
Quantitative Fundus Autofluorescence and Optical Coherence Tomography in PRPH2/RDS- and ABCA4-Associated Disease Exhibiting Phenotypic OverlapTobias Duncker, Stephen H Tsang, Russell L Woods, et al.
Investigative Ophthalmology & Visual Science|March 31, 2017
Quantifying Fundus Autofluorescence in Patients With Retinitis PigmentosaKaspar Schuerch, Russell L Woods, Winston Lee, et al.
Investigative Ophthalmology & Visual Science|May 30, 2015
Near-infrared autofluorescence: its relationship to short-wavelength autofluorescence and optical coherence tomography in recessive stargardt diseaseVivienne C Greenstein, Ari D Schuman, Winston Lee, et al.
Ophthalmic Genetics|March 12, 2011
Elastin rs2301995 polymorphism is not associated with polypoidal choroidal vasculopathy in caucasiansLuiz H Lima, Joanna E Merriam, K Bailey Freund, et al.
Pageof 18

Showing results (71-80 of 180) with videos related to

Sort By:
Pageof 18
Scientific Reports|April 25, 2019
Multi-platform imaging in ABCA4-Associated DiseaseLijuan Chen, Winston Lee, Jose Ronaldo Lima de Carvalho, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 23, 2013
Disruption of the human cone photoreceptor mosaic from a defect in NR2E3 transcription factor function in young adultsSung Pyo Park, In Hwan Hong, Stephen H Tsang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 14, 2009
Phenotypic features of patients with NR2E3 mutationsSophia I Pachydaki, Carolyn C Klaver, Irene A Barbazetto, et al.
Ophthalmic Genetics|November 9, 2011
Disruption in Bruch membrane in patients with Stargardt diseaseSung Pyo Park, Stanley Chang, Rando Allikmets, et al.
Investigative Ophthalmology & Visual Science|July 31, 2014
Choroidal and retinal thickening in severe preeclampsiaAakriti Garg, Ronald J Wapner, Cande V Ananth, et al.
Investigative Ophthalmology & Visual Science|January 31, 2002
Genotype-phenotype analysis of ABCR variants in macular degeneration probands and siblingsPaul S Bernstein, Mark Leppert, Nanda Singh, et al.
Investigative Ophthalmology & Visual Science|May 30, 2015
Quantitative Fundus Autofluorescence and Optical Coherence Tomography in PRPH2/RDS- and ABCA4-Associated Disease Exhibiting Phenotypic OverlapTobias Duncker, Stephen H Tsang, Russell L Woods, et al.
Investigative Ophthalmology & Visual Science|March 31, 2017
Quantifying Fundus Autofluorescence in Patients With Retinitis PigmentosaKaspar Schuerch, Russell L Woods, Winston Lee, et al.
Investigative Ophthalmology & Visual Science|May 30, 2015
Near-infrared autofluorescence: its relationship to short-wavelength autofluorescence and optical coherence tomography in recessive stargardt diseaseVivienne C Greenstein, Ari D Schuman, Winston Lee, et al.
Ophthalmic Genetics|March 12, 2011
Elastin rs2301995 polymorphism is not associated with polypoidal choroidal vasculopathy in caucasiansLuiz H Lima, Joanna E Merriam, K Bailey Freund, et al.
Pageof 18