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Jamie E Craig

Showing results (131-140 of 352) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Screening for glaucomatous disc changes prior to diagnosis of glaucoma in myocilin pedigreesSonya L Bennett, Alex W Hewitt, Johan L Poulsen, et al.
Investigative Ophthalmology & Visual Science|March 8, 2012
Elevation of serum asymmetrical and symmetrical dimethylarginine in patients with advanced glaucomaShahrbanou Javadiyan, Kathryn P Burdon, Malcolm J Whiting, et al.
BMC Research Notes|February 13, 2016
Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataractShari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Human Genetics|January 11, 2003
Analysis of 15 primary open-angle glaucoma families from Australia identifies a founder effect for the Q368STOP mutation of myocilinPaul N Baird, Jamie E Craig, Andrea J Richardson, et al.
Experimental Eye Research|July 6, 2021
Differential gene expression analysis of corneal endothelium indicates involvement of phagocytic activity in Fuchs' endothelial corneal dystrophyAbraham Kuot, Mark A Corbett, Richard A Mills, et al.
Eye (London, England)|November 5, 2024
A generalised computer vision model for improved glaucoma screening using fundus imagesAbadh K Chaurasia, Guei-Sheung Liu, Connor J Greatbatch, et al.
American Journal of Medical Genetics. Part A|March 18, 2009
A novel genetic syndrome characterized by pediatric cataract, dysmorphism, ectodermal features, and developmental delay in an indigenous Australian familyKathryn P Burdon, Shane R Durkin, Mary Burke, et al.
Molecular Vision|September 23, 2008
Genetic analysis of the clusterin gene in pseudoexfoliation syndromeKathryn P Burdon, Shiwani Sharma, Alex W Hewitt, et al.
Clinical Endocrinology|December 31, 2013
Serum selenium status in Graves' disease with and without orbitopathy: a case-control studyJwu Jin Khong, Rebecca F Goldstein, Kerrie M Sanders, et al.
American Journal of Ophthalmology|February 20, 2007
Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutationsAmy C Cohn, Carmel Toomes, Catherine Potter, et al.
Pageof 36

Showing results (131-140 of 352) with videos related to

Sort By:
Pageof 36
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Screening for glaucomatous disc changes prior to diagnosis of glaucoma in myocilin pedigreesSonya L Bennett, Alex W Hewitt, Johan L Poulsen, et al.
Investigative Ophthalmology & Visual Science|March 8, 2012
Elevation of serum asymmetrical and symmetrical dimethylarginine in patients with advanced glaucomaShahrbanou Javadiyan, Kathryn P Burdon, Malcolm J Whiting, et al.
BMC Research Notes|February 13, 2016
Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataractShari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Human Genetics|January 11, 2003
Analysis of 15 primary open-angle glaucoma families from Australia identifies a founder effect for the Q368STOP mutation of myocilinPaul N Baird, Jamie E Craig, Andrea J Richardson, et al.
Experimental Eye Research|July 6, 2021
Differential gene expression analysis of corneal endothelium indicates involvement of phagocytic activity in Fuchs' endothelial corneal dystrophyAbraham Kuot, Mark A Corbett, Richard A Mills, et al.
Eye (London, England)|November 5, 2024
A generalised computer vision model for improved glaucoma screening using fundus imagesAbadh K Chaurasia, Guei-Sheung Liu, Connor J Greatbatch, et al.
American Journal of Medical Genetics. Part A|March 18, 2009
A novel genetic syndrome characterized by pediatric cataract, dysmorphism, ectodermal features, and developmental delay in an indigenous Australian familyKathryn P Burdon, Shane R Durkin, Mary Burke, et al.
Molecular Vision|September 23, 2008
Genetic analysis of the clusterin gene in pseudoexfoliation syndromeKathryn P Burdon, Shiwani Sharma, Alex W Hewitt, et al.
Clinical Endocrinology|December 31, 2013
Serum selenium status in Graves' disease with and without orbitopathy: a case-control studyJwu Jin Khong, Rebecca F Goldstein, Kerrie M Sanders, et al.
American Journal of Ophthalmology|February 20, 2007
Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutationsAmy C Cohn, Carmel Toomes, Catherine Potter, et al.
Pageof 36