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Martin McKibbin

Showing results (51-60 of 106) with videos related to

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Retina (Philadelphia, Pa.)|April 14, 2017
VISUAL ACUITY IMPROVEMENT WHEN SWITCHING FROM RANIBIZUMAB TO AFLIBERCEPT IS NOT SUSTAINEDCecilia S Lee, Alisa J Kim, Douglas Baughman, et al.
American Journal of Human Genetics|April 28, 2006
Quantification of homozygosity in consanguineous individuals with autosomal recessive diseaseC Geoffrey Woods, James Cox, Kelly Springell, et al.
Plos One|August 19, 2014
Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencingChristopher M Watson, Mohammed El-Asrag, David A Parry, et al.
Retina (Philadelphia, Pa.)|February 2, 2023
UNITED KINGDOM DATABASE STUDY OF INTRAVITREAL DEXAMETHASONE IMPLANT (OZURDEX) FOR MACULAR EDEMA RELATED TO RETINAL VEIN OCCLUSIONMohamed Kamel Soliman, Javier Zarranz-Ventura, Usha Chakravarthy, et al.
Genes|January 21, 2023
Effective smMIPs-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UKBenjamin Mc Clinton, Zelia Corradi, Martin McKibbin, et al.
Molecular Vision|July 29, 2010
Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc colobomaManir Ali, Beatriz Buentello-Volante, Martin McKibbin, et al.
Ophthalmology|June 24, 2014
The neovascular age-related macular degeneration database: report 2: incidence, management, and visual outcomes of second treated eyesJavier Zarranz-Ventura, Gerald Liew, Robert L Johnston, et al.
Eye (London, England)|December 15, 2023
Baseline characteristics of eyes with early residual fluid post loading phase of aflibercept therapy in neovascular AMD: PRECISE study report 3Shruti Chandra, Sarega Gurudas, Ian Pearce, et al.
Stem Cells (Dayton, Ohio)|September 16, 2017
An Induced Pluripotent Stem Cell Patient Specific Model of Complement Factor H (Y402H) Polymorphism Displays Characteristic Features of Age-Related Macular Degeneration and Indicates a Beneficial Role for UV Light ExposureDean Hallam, Joseph Collin, Sanja Bojic, et al.
American Journal of Human Genetics|October 27, 2009
Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosaAlice E Davidson, Ian D Millar, Jill E Urquhart, et al.
Pageof 11

Showing results (51-60 of 106) with videos related to

Sort By:
Pageof 11
Retina (Philadelphia, Pa.)|April 14, 2017
VISUAL ACUITY IMPROVEMENT WHEN SWITCHING FROM RANIBIZUMAB TO AFLIBERCEPT IS NOT SUSTAINEDCecilia S Lee, Alisa J Kim, Douglas Baughman, et al.
American Journal of Human Genetics|April 28, 2006
Quantification of homozygosity in consanguineous individuals with autosomal recessive diseaseC Geoffrey Woods, James Cox, Kelly Springell, et al.
Plos One|August 19, 2014
Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencingChristopher M Watson, Mohammed El-Asrag, David A Parry, et al.
Retina (Philadelphia, Pa.)|February 2, 2023
UNITED KINGDOM DATABASE STUDY OF INTRAVITREAL DEXAMETHASONE IMPLANT (OZURDEX) FOR MACULAR EDEMA RELATED TO RETINAL VEIN OCCLUSIONMohamed Kamel Soliman, Javier Zarranz-Ventura, Usha Chakravarthy, et al.
Genes|January 21, 2023
Effective smMIPs-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UKBenjamin Mc Clinton, Zelia Corradi, Martin McKibbin, et al.
Molecular Vision|July 29, 2010
Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc colobomaManir Ali, Beatriz Buentello-Volante, Martin McKibbin, et al.
Ophthalmology|June 24, 2014
The neovascular age-related macular degeneration database: report 2: incidence, management, and visual outcomes of second treated eyesJavier Zarranz-Ventura, Gerald Liew, Robert L Johnston, et al.
Eye (London, England)|December 15, 2023
Baseline characteristics of eyes with early residual fluid post loading phase of aflibercept therapy in neovascular AMD: PRECISE study report 3Shruti Chandra, Sarega Gurudas, Ian Pearce, et al.
Stem Cells (Dayton, Ohio)|September 16, 2017
An Induced Pluripotent Stem Cell Patient Specific Model of Complement Factor H (Y402H) Polymorphism Displays Characteristic Features of Age-Related Macular Degeneration and Indicates a Beneficial Role for UV Light ExposureDean Hallam, Joseph Collin, Sanja Bojic, et al.
American Journal of Human Genetics|October 27, 2009
Missense mutations in a retinal pigment epithelium protein, bestrophin-1, cause retinitis pigmentosaAlice E Davidson, Ian D Millar, Jill E Urquhart, et al.
Pageof 11