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Michael B Gorin

Showing results (11-20 of 101) with videos related to

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Retinal Cases & Brief Reports|February 23, 2018
A CASE OF INTRARETINAL PERIPAPILLARY NEOVASCULARIZATION IN ABCA4-RELATED RETINOPATHYJuliet O Essilfie, An Huynh, Michael B Gorin, et al.
Cornea|November 1, 2002
Fluorescein-potentiated argon laser therapy improves symptoms and appearance of corneal neovascularizationY Jerold Gordon, Rupinder K Mann, Tammy S Mah, et al.
BMC Bioinformatics|April 19, 2015
dbVOR: a database system for importing pedigree, phenotype and genotype data and exporting selected subsetsRobert V Baron, Yvette P Conley, Michael B Gorin, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 23, 2010
Novel KRIT1/CCM1 mutation in a patient with retinal cavernous hemangioma and cerebral cavernous malformationShantan Reddy, Michael B Gorin, Tara A McCannel, et al.
American Journal of Ophthalmology|July 6, 2004
A novel compound heterozygous mutation in the cellular retinaldehyde-binding protein gene (RLBP1) in a patient with retinitis punctata albescensF Yesim K Demirci, Brian W Rigatti, Tammy S Mah, et al.
American Journal of Ophthalmology|January 3, 2006
A novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa and Coats'-like exudative vasculopathyF Yesim K Demirci, Brian W Rigatti, Tammy S Mah, et al.
Journal of Visualized Experiments : Jove|January 7, 2017
An Alternative and Validated Injection Method for Accessing the Subretinal Space via a Transcleral Posterior ApproachSachin Parikh, Andrew Le, Julian Davenport, et al.
Translational Vision Science & Technology|May 26, 2021
Assessing the Clinical Utility of Expanded Macular OCTs Using Machine LearningAndrew C Lin, Cecilia S Lee, Marian Blazes, et al.
Plos Genetics|February 7, 2009
Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiersJohanna Jakobsdottir, Michael B Gorin, Yvette P Conley, et al.
Plos One|May 22, 2008
C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genesJohanna Jakobsdottir, Yvette P Conley, Daniel E Weeks, et al.
Pageof 11

Showing results (11-20 of 101) with videos related to

Sort By:
Pageof 11
Retinal Cases & Brief Reports|February 23, 2018
A CASE OF INTRARETINAL PERIPAPILLARY NEOVASCULARIZATION IN ABCA4-RELATED RETINOPATHYJuliet O Essilfie, An Huynh, Michael B Gorin, et al.
Cornea|November 1, 2002
Fluorescein-potentiated argon laser therapy improves symptoms and appearance of corneal neovascularizationY Jerold Gordon, Rupinder K Mann, Tammy S Mah, et al.
BMC Bioinformatics|April 19, 2015
dbVOR: a database system for importing pedigree, phenotype and genotype data and exporting selected subsetsRobert V Baron, Yvette P Conley, Michael B Gorin, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 23, 2010
Novel KRIT1/CCM1 mutation in a patient with retinal cavernous hemangioma and cerebral cavernous malformationShantan Reddy, Michael B Gorin, Tara A McCannel, et al.
American Journal of Ophthalmology|July 6, 2004
A novel compound heterozygous mutation in the cellular retinaldehyde-binding protein gene (RLBP1) in a patient with retinitis punctata albescensF Yesim K Demirci, Brian W Rigatti, Tammy S Mah, et al.
American Journal of Ophthalmology|January 3, 2006
A novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa and Coats'-like exudative vasculopathyF Yesim K Demirci, Brian W Rigatti, Tammy S Mah, et al.
Journal of Visualized Experiments : Jove|January 7, 2017
An Alternative and Validated Injection Method for Accessing the Subretinal Space via a Transcleral Posterior ApproachSachin Parikh, Andrew Le, Julian Davenport, et al.
Translational Vision Science & Technology|May 26, 2021
Assessing the Clinical Utility of Expanded Macular OCTs Using Machine LearningAndrew C Lin, Cecilia S Lee, Marian Blazes, et al.
Plos Genetics|February 7, 2009
Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiersJohanna Jakobsdottir, Michael B Gorin, Yvette P Conley, et al.
Plos One|May 22, 2008
C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genesJohanna Jakobsdottir, Yvette P Conley, Daniel E Weeks, et al.
Pageof 11