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Rando Allikmets

Showing results (81-90 of 180) with videos related to

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The New England Journal of Medicine|May 27, 2009
Geographic atrophy in age-related macular degeneration and TLR3Rando Allikmets, Arthur A Bergen, Michael Dean, et al.
Investigative Ophthalmology & Visual Science|May 31, 2018
Mutations in GPR143/OA1 and ABCA4 Inform Interpretations of Short-Wavelength and Near-Infrared Fundus AutofluorescenceMaarjaliis Paavo, Jin Zhao, Hye Jin Kim, et al.
Investigative Ophthalmology & Visual Science|April 24, 2023
Insights Into PROM1-Macular Disease Using Multimodal ImagingMaarjaliis Paavo, Winston Lee, Rait Parmann, et al.
Brain Research. Molecular Brain Research|December 8, 2004
Retinal degeneration in Aipl1-deficient mice: a new genetic model of Leber congenital amaurosisMichael A Dyer, Stacy L Donovan, Jiakun Zhang, et al.
Ophthalmic Genetics|December 29, 2007
Pseudo-vitelliform macular detachment and cuticular drusen: exclusion of 6 candidate genesIrene A Barbazetto, Nicolas A Yannuzzi, Christina M Klais, et al.
JAMA Ophthalmology|August 31, 2013
Expanded clinical spectrum of enhanced S-cone syndromeSuzanne Yzer, Irene Barbazetto, Rando Allikmets, et al.
Journal of Clinical & Experimental Ophthalmology|January 11, 2014
Functional Analysis of Retinal Flecks in Stargardt DiseaseTommaso Verdina, Stephen H Tsang, Vivienne C Greenstein, 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.
Ophthalmic Genetics|February 18, 2015
Whole Exome Sequencing Identifies an Adult-Onset Case of Methylmalonic Aciduria and Homocystinuria Type C (cblC) with Non-Syndromic Bull's Eye MaculopathyFrederick T Collison, Yajing Angela Xie, Tomasz Gambin, et al.
Pageof 18

Showing results (81-90 of 180) with videos related to

Sort By:
Pageof 18
The New England Journal of Medicine|May 27, 2009
Geographic atrophy in age-related macular degeneration and TLR3Rando Allikmets, Arthur A Bergen, Michael Dean, et al.
Investigative Ophthalmology & Visual Science|May 31, 2018
Mutations in GPR143/OA1 and ABCA4 Inform Interpretations of Short-Wavelength and Near-Infrared Fundus AutofluorescenceMaarjaliis Paavo, Jin Zhao, Hye Jin Kim, et al.
Investigative Ophthalmology & Visual Science|April 24, 2023
Insights Into PROM1-Macular Disease Using Multimodal ImagingMaarjaliis Paavo, Winston Lee, Rait Parmann, et al.
Brain Research. Molecular Brain Research|December 8, 2004
Retinal degeneration in Aipl1-deficient mice: a new genetic model of Leber congenital amaurosisMichael A Dyer, Stacy L Donovan, Jiakun Zhang, et al.
Ophthalmic Genetics|December 29, 2007
Pseudo-vitelliform macular detachment and cuticular drusen: exclusion of 6 candidate genesIrene A Barbazetto, Nicolas A Yannuzzi, Christina M Klais, et al.
JAMA Ophthalmology|August 31, 2013
Expanded clinical spectrum of enhanced S-cone syndromeSuzanne Yzer, Irene Barbazetto, Rando Allikmets, et al.
Journal of Clinical & Experimental Ophthalmology|January 11, 2014
Functional Analysis of Retinal Flecks in Stargardt DiseaseTommaso Verdina, Stephen H Tsang, Vivienne C Greenstein, 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.
Ophthalmic Genetics|February 18, 2015
Whole Exome Sequencing Identifies an Adult-Onset Case of Methylmalonic Aciduria and Homocystinuria Type C (cblC) with Non-Syndromic Bull's Eye MaculopathyFrederick T Collison, Yajing Angela Xie, Tomasz Gambin, et al.
Pageof 18