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Jonathan B Ruddle

Showing results (31-40 of 79) with videos related to

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Clinical & Experimental Ophthalmology|July 14, 2011
Telemedicine model to prevent blindness from familial glaucomaSandra E Staffieri, Jonathan B Ruddle, Lisa S Kearns, et al.
Experimental Eye Research|July 6, 2010
A geometric morphometric assessment of the optic cup in glaucomaPaul G Sanfilippo, Andrea Cardini, Ian A Sigal, et al.
Cornea|March 30, 2022
Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 VariantsMallika Prem Senthil, Lachlan S W Knight, Deepa Taranath, et al.
Molecular Vision|April 26, 2006
The PITX3 gene in posterior polar congenital cataract in AustraliaKathryn P Burdon, James D McKay, M Gabriela Wirth, et al.
Clinical & Experimental Ophthalmology|March 21, 2012
Bleb vascularity following post-trabeculectomy subconjunctival bevacizumab: a pilot studyBrian E Chua, Dan Q Nguyen, Queena Qin, et al.
Investigative Ophthalmology & Visual Science|April 19, 2011
Ophthalmic phenotypes and the representativeness of twin data for the general populationPaul G Sanfilippo, Sarah E Medland, Alex W Hewitt, et al.
The Journal of Clinical Investigation|December 1, 2022
Thrombospondin 1 missense alleles induce extracellular matrix protein aggregation and TM dysfunction in congenital glaucomaHaojie Fu, Owen M Siggs, Lachlan Sw Knight, et al.
Ophthalmology|December 21, 2016
Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk IndividualsEmmanuelle Souzeau, Kien Hou Tram, Martin Witney, et al.
Scientific Reports|March 5, 2024
Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional surveyAlexis Ceecee Britten-Jones, Joshua Schultz, Heather G Mack, et al.
Molecular Vision|March 10, 2015
CYP1B1 copy number variation is not a major contributor to primary congenital glaucomaEmmanuelle Souzeau, Melanie Hayes, Jonathan B Ruddle, et al.
Pageof 8

Showing results (31-40 of 79) with videos related to

Sort By:
Pageof 8
Clinical & Experimental Ophthalmology|July 14, 2011
Telemedicine model to prevent blindness from familial glaucomaSandra E Staffieri, Jonathan B Ruddle, Lisa S Kearns, et al.
Experimental Eye Research|July 6, 2010
A geometric morphometric assessment of the optic cup in glaucomaPaul G Sanfilippo, Andrea Cardini, Ian A Sigal, et al.
Cornea|March 30, 2022
Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 VariantsMallika Prem Senthil, Lachlan S W Knight, Deepa Taranath, et al.
Molecular Vision|April 26, 2006
The PITX3 gene in posterior polar congenital cataract in AustraliaKathryn P Burdon, James D McKay, M Gabriela Wirth, et al.
Clinical & Experimental Ophthalmology|March 21, 2012
Bleb vascularity following post-trabeculectomy subconjunctival bevacizumab: a pilot studyBrian E Chua, Dan Q Nguyen, Queena Qin, et al.
Investigative Ophthalmology & Visual Science|April 19, 2011
Ophthalmic phenotypes and the representativeness of twin data for the general populationPaul G Sanfilippo, Sarah E Medland, Alex W Hewitt, et al.
The Journal of Clinical Investigation|December 1, 2022
Thrombospondin 1 missense alleles induce extracellular matrix protein aggregation and TM dysfunction in congenital glaucomaHaojie Fu, Owen M Siggs, Lachlan Sw Knight, et al.
Ophthalmology|December 21, 2016
Myocilin Predictive Genetic Testing for Primary Open-Angle Glaucoma Leads to Early Identification of At-Risk IndividualsEmmanuelle Souzeau, Kien Hou Tram, Martin Witney, et al.
Scientific Reports|March 5, 2024
Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional surveyAlexis Ceecee Britten-Jones, Joshua Schultz, Heather G Mack, et al.
Molecular Vision|March 10, 2015
CYP1B1 copy number variation is not a major contributor to primary congenital glaucomaEmmanuelle Souzeau, Melanie Hayes, Jonathan B Ruddle, et al.
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