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John R Grigg

Showing results (21-30 of 92) with videos related to

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Clinical & Experimental Ophthalmology|March 2, 2016
Changing patterns in paediatric optic atrophy aetiology: 1979 to 2015Linda Zheng, Helen Hyun-Jin Do, Trent Sandercoe, et al.
Acta Ophthalmologica|December 1, 2020
Natural history and clinical biomarkers of progression in X-linked retinitis pigmentosa: a systematic reviewMark Zada, Elisa E Cornish, Clare L Fraser, et al.
Journal of Glaucoma|November 10, 2015
Uveal Effusion: Clinical Features, Management, and Visual Outcomes in a Retrospective Case SeriesParth R Shah, Jayshan Yohendran, Alex P Hunyor, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|November 12, 2013
The importance of electrophysiology in revealing a complete homozygous deletion of KCNV2John R Grigg, Graham E Holder, Francis A Billson, et al.
International Journal of Retina and Vitreous|July 14, 2018
Idiopathic full thickness macular hole in a 10-year-old girlLi-Anne S Lim, Guillermo Fernandez-Sanz, Steven Levasseur, et al.
Journal of Paediatrics and Child Health|August 6, 2025
A Practical Guide to Genetic Eye Conditions for PaediatriciansRichard Lin, Alan Ma, Benjamin M Nash, et al.
Ophthalmic Genetics|June 1, 2023
<i>IMPDH1</i>-associated autosomal dominant retinitis pigmentosa: natural history of novel variant Lys314Gln and a comprehensive literature searchDhimas H Sakti, Elisa E Cornish, Benjamin M Nash, et al.
Ophthalmic Research|April 21, 2017
Choroidal Thickness and Microperimetry Sensitivity in Age-Related Macular DegenerationGeoffrey K Broadhead, Thomas Hong, Peter McCluskey, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|February 14, 2015
Descemetorhexis for Fuchs' dystrophyGregory Moloney, U-Teng Chan, Alex Hamilton, et al.
BMC Family Practice|December 1, 2021
Barriers and facilitators to diabetic retinopathy screening within Australian primary careMatthew J G Watson, Peter J McCluskey, John R Grigg, et al.
Pageof 10

Showing results (21-30 of 92) with videos related to

Sort By:
Pageof 10
Clinical & Experimental Ophthalmology|March 2, 2016
Changing patterns in paediatric optic atrophy aetiology: 1979 to 2015Linda Zheng, Helen Hyun-Jin Do, Trent Sandercoe, et al.
Acta Ophthalmologica|December 1, 2020
Natural history and clinical biomarkers of progression in X-linked retinitis pigmentosa: a systematic reviewMark Zada, Elisa E Cornish, Clare L Fraser, et al.
Journal of Glaucoma|November 10, 2015
Uveal Effusion: Clinical Features, Management, and Visual Outcomes in a Retrospective Case SeriesParth R Shah, Jayshan Yohendran, Alex P Hunyor, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|November 12, 2013
The importance of electrophysiology in revealing a complete homozygous deletion of KCNV2John R Grigg, Graham E Holder, Francis A Billson, et al.
International Journal of Retina and Vitreous|July 14, 2018
Idiopathic full thickness macular hole in a 10-year-old girlLi-Anne S Lim, Guillermo Fernandez-Sanz, Steven Levasseur, et al.
Journal of Paediatrics and Child Health|August 6, 2025
A Practical Guide to Genetic Eye Conditions for PaediatriciansRichard Lin, Alan Ma, Benjamin M Nash, et al.
Ophthalmic Genetics|June 1, 2023
<i>IMPDH1</i>-associated autosomal dominant retinitis pigmentosa: natural history of novel variant Lys314Gln and a comprehensive literature searchDhimas H Sakti, Elisa E Cornish, Benjamin M Nash, et al.
Ophthalmic Research|April 21, 2017
Choroidal Thickness and Microperimetry Sensitivity in Age-Related Macular DegenerationGeoffrey K Broadhead, Thomas Hong, Peter McCluskey, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|February 14, 2015
Descemetorhexis for Fuchs' dystrophyGregory Moloney, U-Teng Chan, Alex Hamilton, et al.
BMC Family Practice|December 1, 2021
Barriers and facilitators to diabetic retinopathy screening within Australian primary careMatthew J G Watson, Peter J McCluskey, John R Grigg, et al.
Pageof 10