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Gerald A Fishman

Showing results (131-140 of 176) with videos related to

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Investigative Ophthalmology & Visual Science|June 30, 2004
Dark adaptation of rod photoreceptors in normal subjects, and in patients with Stargardt disease and an ABCA4 mutationJennifer J Kang Derwent, Deborah J Derlacki, John R Hetling, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 23, 2005
Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6Thaddeus P Dryja, Terri L McGee, Eliot L Berson, et al.
Investigative Ophthalmology & Visual Science|July 23, 2011
Photoreceptor structure and function in patients with congenital achromatopsiaMohamed A Genead, Gerald A Fishman, Jungtae Rha, et al.
Investigative Ophthalmology & Visual Science|September 14, 2011
Analysis of the ABCA4 gene by next-generation sequencingJana Zernant, Carl Schubert, Kate M Im, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 8, 2021
Pathognomonic macular ripples are revealed by polarized infrared retinal imagingDarius Ansari, Poulami P Borkar, Patricia L Davis, et al.
American Journal of Ophthalmology|July 31, 2003
Comparison of the clinical expression of retinitis pigmentosa associated with rhodopsin mutations at codon 347 and codon 23Kean T Oh, Reid Longmuir, Dawn M Oh, et al.
Human Mutation|July 29, 2014
Genetic and clinical analysis of ABCA4-associated disease in African American patientsJana Zernant, Frederick T Collison, Winston Lee, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 18, 2011
Autoantibodies in melanoma-associated retinopathy target TRPM1 cation channels of retinal ON bipolar cellsAnuradha Dhingra, Marie E Fina, Adam Neinstein, et al.
American Journal of Ophthalmology|February 19, 2017
Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D MutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Science Translational Medicine|December 10, 2020
Gene dosage manipulation alleviates manifestations of hereditary <i>PAX6</i> haploinsufficiency in miceBehnam Rabiee, Khandaker N Anwar, Xiang Shen, et al.
Pageof 18

Showing results (131-140 of 176) with videos related to

Sort By:
Pageof 18
Investigative Ophthalmology & Visual Science|June 30, 2004
Dark adaptation of rod photoreceptors in normal subjects, and in patients with Stargardt disease and an ABCA4 mutationJennifer J Kang Derwent, Deborah J Derlacki, John R Hetling, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 23, 2005
Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6Thaddeus P Dryja, Terri L McGee, Eliot L Berson, et al.
Investigative Ophthalmology & Visual Science|July 23, 2011
Photoreceptor structure and function in patients with congenital achromatopsiaMohamed A Genead, Gerald A Fishman, Jungtae Rha, et al.
Investigative Ophthalmology & Visual Science|September 14, 2011
Analysis of the ABCA4 gene by next-generation sequencingJana Zernant, Carl Schubert, Kate M Im, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 8, 2021
Pathognomonic macular ripples are revealed by polarized infrared retinal imagingDarius Ansari, Poulami P Borkar, Patricia L Davis, et al.
American Journal of Ophthalmology|July 31, 2003
Comparison of the clinical expression of retinitis pigmentosa associated with rhodopsin mutations at codon 347 and codon 23Kean T Oh, Reid Longmuir, Dawn M Oh, et al.
Human Mutation|July 29, 2014
Genetic and clinical analysis of ABCA4-associated disease in African American patientsJana Zernant, Frederick T Collison, Winston Lee, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 18, 2011
Autoantibodies in melanoma-associated retinopathy target TRPM1 cation channels of retinal ON bipolar cellsAnuradha Dhingra, Marie E Fina, Adam Neinstein, et al.
American Journal of Ophthalmology|February 19, 2017
Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D MutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Science Translational Medicine|December 10, 2020
Gene dosage manipulation alleviates manifestations of hereditary <i>PAX6</i> haploinsufficiency in miceBehnam Rabiee, Khandaker N Anwar, Xiang Shen, et al.
Pageof 18