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Rando Allikmets

Showing results (11-20 of 180) with videos related to

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Investigative Ophthalmology & Visual Science|June 23, 2016
Quantitative Autofluorescence and ABCA4 DiseaseRando Allikmets, Tobias Duncker, Winston Lee, et al.
American Journal of Ophthalmology|May 2, 2009
Peripapillary retinal nerve fiber layer thinning in patients with autosomal recessive cone-rod dystrophySirichai Pasadhika, Gerald A Fishman, Rando Allikmets, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 5, 2005
Isolation and characterization of a retinal pigment epithelial cell fluorophore: an all-trans-retinal dimer conjugateNathan E Fishkin, Janet R Sparrow, Rando Allikmets, et al.
American Journal of Ophthalmology|February 13, 2010
Preimplantation genetic diagnosis for stargardt diseaseMahsa A Sohrab, Rando Allikmets, Michael M Guarnaccia, et al.
American Journal of Ophthalmology|July 29, 2018
Deep Scleral Exposure: A Degenerative Outcome of End-Stage Stargardt DiseaseWinston Lee, Jana Zernant, Takayuki Nagasaki, et al.
Journal of Neuroscience Research|April 28, 2018
Photoreceptor cells as a source of fundus autofluorescence in recessive Stargardt diseaseMaarjaliis Paavo, Winston Lee, Rando Allikmets, et al.
Investigative Ophthalmology & Visual Science|July 7, 2009
The natural history of stargardt disease with specific sequence mutation in the ABCA4 geneMohamed A Genead, Gerald A Fishman, Edwin M Stone, et al.
Investigative Ophthalmology & Visual Science|October 11, 2014
Structural and genetic assessment of the ABCA4-associated optical gap phenotypeKalev Nõupuu, Winston Lee, Jana Zernant, et al.
Progress in Retinal and Eye Research|April 13, 2020
Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutationsFrans P M Cremers, Winston Lee, Rob W J Collin, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|December 20, 2013
Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation (D100G) in the GUCA1A geneEva Nong, Winston Lee, Joanna E Merriam, et al.
Pageof 18

Showing results (11-20 of 180) with videos related to

Sort By:
Pageof 18
Investigative Ophthalmology & Visual Science|June 23, 2016
Quantitative Autofluorescence and ABCA4 DiseaseRando Allikmets, Tobias Duncker, Winston Lee, et al.
American Journal of Ophthalmology|May 2, 2009
Peripapillary retinal nerve fiber layer thinning in patients with autosomal recessive cone-rod dystrophySirichai Pasadhika, Gerald A Fishman, Rando Allikmets, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 5, 2005
Isolation and characterization of a retinal pigment epithelial cell fluorophore: an all-trans-retinal dimer conjugateNathan E Fishkin, Janet R Sparrow, Rando Allikmets, et al.
American Journal of Ophthalmology|February 13, 2010
Preimplantation genetic diagnosis for stargardt diseaseMahsa A Sohrab, Rando Allikmets, Michael M Guarnaccia, et al.
American Journal of Ophthalmology|July 29, 2018
Deep Scleral Exposure: A Degenerative Outcome of End-Stage Stargardt DiseaseWinston Lee, Jana Zernant, Takayuki Nagasaki, et al.
Journal of Neuroscience Research|April 28, 2018
Photoreceptor cells as a source of fundus autofluorescence in recessive Stargardt diseaseMaarjaliis Paavo, Winston Lee, Rando Allikmets, et al.
Investigative Ophthalmology & Visual Science|July 7, 2009
The natural history of stargardt disease with specific sequence mutation in the ABCA4 geneMohamed A Genead, Gerald A Fishman, Edwin M Stone, et al.
Investigative Ophthalmology & Visual Science|October 11, 2014
Structural and genetic assessment of the ABCA4-associated optical gap phenotypeKalev Nõupuu, Winston Lee, Jana Zernant, et al.
Progress in Retinal and Eye Research|April 13, 2020
Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutationsFrans P M Cremers, Winston Lee, Rob W J Collin, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|December 20, 2013
Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation (D100G) in the GUCA1A geneEva Nong, Winston Lee, Joanna E Merriam, et al.
Pageof 18