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Gerald A Fishman

Showing results (111-120 of 176) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|August 10, 2005
Stop mutations in exon 6 of the choroideremia gene, CHM, associated with preservation of the electroretinogramPeter J Francis, Gerald A Fishman, Karmen M Trzupek, et al.
Ophthalmic Genetics|September 30, 2014
Retinal Histopathology in Eyes from a Patient with Stargardt disease caused by Compound Heterozygous ABCA4 MutationsVera L Bonilha, Mary E Rayborn, Brent A Bell, et al.
Investigative Ophthalmology & Visual Science|July 25, 2015
Objective Analysis of Hyperreflective Outer Retinal Bands Imaged by Optical Coherence Tomography in Patients With Stargardt DiseaseJason C Park, Frederick T Collison, Gerald A Fishman, et al.
Frontiers in Cell and Developmental Biology|November 6, 2020
Cellular Changes in Retinas From Patients With <i>BEST1</i> MutationsVera L Bonilha, Brent A Bell, Meghan J DeBenedictis, et al.
Investigative Ophthalmology & Visual Science|June 8, 2014
In vivo imaging of human cone photoreceptor inner segmentsDrew Scoles, Yusufu N Sulai, Christopher S Langlo, et al.
Retina (Philadelphia, Pa.)|September 12, 2018
CLINICAL CHARACTERIZATION OF STARGARDT DISEASE PATIENTS WITH THE p.N1868I ABCA4 MUTATIONFrederick T Collison, Winston Lee, Gerald A Fishman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
Discordant phenotypes in fraternal twins having an identical mutation in exon ORF15 of the RPGR geneSaloni Walia, Gerald A Fishman, Anand Swaroop, et al.
Investigative Ophthalmology & Visual Science|May 29, 2019
Characteristic Ocular Features in Cases of Autosomal Recessive PROM1 Cone-Rod DystrophyFrederick T Collison, Gerald A Fishman, Takayuki Nagasaki, et al.
Investigative Ophthalmology & Visual Science|December 5, 2009
Differential macular morphology in patients with RPE65-, CEP290-, GUCY2D-, and AIPL1-related Leber congenital amaurosisSirichai Pasadhika, Gerald A Fishman, Edwin M Stone, et al.
American Journal of Ophthalmology|October 7, 2008
Relation of response to treatment with dorzolamide in X-linked retinoschisis to the mechanism of functional loss in retinoschisinSaloni Walia, Gerald A Fishman, Robert S Molday, et al.
Pageof 18

Showing results (111-120 of 176) with videos related to

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Pageof 18
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 10, 2005
Stop mutations in exon 6 of the choroideremia gene, CHM, associated with preservation of the electroretinogramPeter J Francis, Gerald A Fishman, Karmen M Trzupek, et al.
Ophthalmic Genetics|September 30, 2014
Retinal Histopathology in Eyes from a Patient with Stargardt disease caused by Compound Heterozygous ABCA4 MutationsVera L Bonilha, Mary E Rayborn, Brent A Bell, et al.
Investigative Ophthalmology & Visual Science|July 25, 2015
Objective Analysis of Hyperreflective Outer Retinal Bands Imaged by Optical Coherence Tomography in Patients With Stargardt DiseaseJason C Park, Frederick T Collison, Gerald A Fishman, et al.
Frontiers in Cell and Developmental Biology|November 6, 2020
Cellular Changes in Retinas From Patients With <i>BEST1</i> MutationsVera L Bonilha, Brent A Bell, Meghan J DeBenedictis, et al.
Investigative Ophthalmology & Visual Science|June 8, 2014
In vivo imaging of human cone photoreceptor inner segmentsDrew Scoles, Yusufu N Sulai, Christopher S Langlo, et al.
Retina (Philadelphia, Pa.)|September 12, 2018
CLINICAL CHARACTERIZATION OF STARGARDT DISEASE PATIENTS WITH THE p.N1868I ABCA4 MUTATIONFrederick T Collison, Winston Lee, Gerald A Fishman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
Discordant phenotypes in fraternal twins having an identical mutation in exon ORF15 of the RPGR geneSaloni Walia, Gerald A Fishman, Anand Swaroop, et al.
Investigative Ophthalmology & Visual Science|May 29, 2019
Characteristic Ocular Features in Cases of Autosomal Recessive PROM1 Cone-Rod DystrophyFrederick T Collison, Gerald A Fishman, Takayuki Nagasaki, et al.
Investigative Ophthalmology & Visual Science|December 5, 2009
Differential macular morphology in patients with RPE65-, CEP290-, GUCY2D-, and AIPL1-related Leber congenital amaurosisSirichai Pasadhika, Gerald A Fishman, Edwin M Stone, et al.
American Journal of Ophthalmology|October 7, 2008
Relation of response to treatment with dorzolamide in X-linked retinoschisis to the mechanism of functional loss in retinoschisinSaloni Walia, Gerald A Fishman, Robert S Molday, et al.
Pageof 18