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A Mackey

Showing results (461-470 of 763) with videos related to

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The Journal of Laryngology and Otology|August 5, 2021
Olfactory dysfunction at six months after coronavirus disease 2019 infectionS R Leedman, M Sheeraz, P G Sanfilippo, et al.
International Journal of Occupational and Environmental Health|May 7, 2005
A global survey of occupational health competencies and curriculumGeorge L Delclos, Karie A Bright, Arch I Carson, et al.
Ophthalmology. Retina|May 14, 2022
Prevalence of Toxoplasmic Retinochoroiditis in an Australian Adult Population: A Community-Based StudyLisia B Ferreira, João M Furtado, Jason Charng, et al.
Plos One|July 7, 2011
Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophyNicole J Van Bergen, Jonathan G Crowston, Lisa S Kearns, et al.
Cornea|December 8, 2011
Role of the TCF4 gene intronic variant in normal variation of corneal endotheliumDavid A Mackey, Nicole M Warrington, Alex W Hewitt, et al.
Journal of Medical Genetics|August 3, 2004
A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetranceK P Burdon, M G Wirth, D A Mackey, et al.
Human Molecular Genetics|November 27, 2007
Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic peopleAlex W Hewitt, Shiwani Sharma, Kathryn P Burdon, et al.
American Journal of Ophthalmology|July 31, 2012
Genetic investigation into the endophenotypic status of central corneal thickness and optic disc parameters in relation to open-angle glaucomaDavid P Dimasi, Kathryn P Burdon, Alex W Hewitt, et al.
Translational Vision Science & Technology|July 12, 2022
The Relationship Between Fetal Growth and Retinal Nerve Fiber Layer Thickness in a Cohort of Young AdultsKathleen I C Dyer, Paul G Sanfilippo, Seyhan Yazar, et al.
Eye (London, England)|November 27, 2010
Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutationsA C Cohn, C Turnbull, J B Ruddle, et al.
Pageof 77

Showing results (461-470 of 763) with videos related to

Sort By:
Pageof 77
The Journal of Laryngology and Otology|August 5, 2021
Olfactory dysfunction at six months after coronavirus disease 2019 infectionS R Leedman, M Sheeraz, P G Sanfilippo, et al.
International Journal of Occupational and Environmental Health|May 7, 2005
A global survey of occupational health competencies and curriculumGeorge L Delclos, Karie A Bright, Arch I Carson, et al.
Ophthalmology. Retina|May 14, 2022
Prevalence of Toxoplasmic Retinochoroiditis in an Australian Adult Population: A Community-Based StudyLisia B Ferreira, João M Furtado, Jason Charng, et al.
Plos One|July 7, 2011
Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophyNicole J Van Bergen, Jonathan G Crowston, Lisa S Kearns, et al.
Cornea|December 8, 2011
Role of the TCF4 gene intronic variant in normal variation of corneal endotheliumDavid A Mackey, Nicole M Warrington, Alex W Hewitt, et al.
Journal of Medical Genetics|August 3, 2004
A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetranceK P Burdon, M G Wirth, D A Mackey, et al.
Human Molecular Genetics|November 27, 2007
Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic peopleAlex W Hewitt, Shiwani Sharma, Kathryn P Burdon, et al.
American Journal of Ophthalmology|July 31, 2012
Genetic investigation into the endophenotypic status of central corneal thickness and optic disc parameters in relation to open-angle glaucomaDavid P Dimasi, Kathryn P Burdon, Alex W Hewitt, et al.
Translational Vision Science & Technology|July 12, 2022
The Relationship Between Fetal Growth and Retinal Nerve Fiber Layer Thickness in a Cohort of Young AdultsKathleen I C Dyer, Paul G Sanfilippo, Seyhan Yazar, et al.
Eye (London, England)|November 27, 2010
Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutationsA C Cohn, C Turnbull, J B Ruddle, et al.
Pageof 77