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R Grigg

Showing results (131-140 of 150) with videos related to

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Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 29, 2025
Understanding the phenotype of genetically associated electronegative ERG retinopathies: comparing the full-field ERG b:a ratioChristopher A Ovens, Elisa E Cornish, Haipha Ali, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 18, 2024
ISCEV and IPS guideline for the full-field stimulus test (FST)J K Jolly, J R Grigg, A M McKendrick, et al.
Gene Therapy|October 1, 2022
Survey of perspectives of people with inherited retinal diseases on ocular gene therapy in AustraliaHeather G Mack, Alexis Ceecee Britten-Jones, Myra B McGuinness, et al.
European Journal of Human Genetics : EJHG|February 26, 2021
Heterozygous COL9A3 variants cause severe peripheral vitreoretinal degeneration and retinal detachmentBenjamin M Nash, Christopher J G Watson, Edward Hughes, et al.
Stem Cells International|December 23, 2021
Evaluation for Retinal Therapy for <i>RPE65</i> Variation Assessed in hiPSC Retinal Pigment Epithelial CellsBenjamin M Nash, To Ha Loi, Milan Fernando, et al.
BMJ Open Ophthalmology|November 19, 2021
Efficient capture of high-quality real-world data on treatments for glaucoma: the Fight Glaucoma Blindness! RegistryMitchell Lawlor, Vuong Nguyen, Anne Brooks, et al.
Human Mutation|December 24, 2015
Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation SequencingAlan S Ma, John R Grigg, Gladys Ho, et al.
Human Mutation|May 12, 2007
Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocationRobyn V Jamieson, Nicola Farrar, Katrina Stewart, et al.
Translational Vision Science & Technology|May 20, 2022
Electrophysiological Assessment in Birdshot Chorioretinopathy: Flicker Electroretinograms Recorded With a Handheld DeviceAnna M Waldie, Angharad E Hobby, Isabelle Chow, et al.
BMJ Open|September 30, 2025
Australian research priorities for inherited retinal diseases: a James Lind Alliance priority setting partnershipEden G Robertson, Kate Hetherington, Meredith Prain, et al.
Pageof 15

Showing results (131-140 of 150) with videos related to

Sort By:
Pageof 15
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 29, 2025
Understanding the phenotype of genetically associated electronegative ERG retinopathies: comparing the full-field ERG b:a ratioChristopher A Ovens, Elisa E Cornish, Haipha Ali, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 18, 2024
ISCEV and IPS guideline for the full-field stimulus test (FST)J K Jolly, J R Grigg, A M McKendrick, et al.
Gene Therapy|October 1, 2022
Survey of perspectives of people with inherited retinal diseases on ocular gene therapy in AustraliaHeather G Mack, Alexis Ceecee Britten-Jones, Myra B McGuinness, et al.
European Journal of Human Genetics : EJHG|February 26, 2021
Heterozygous COL9A3 variants cause severe peripheral vitreoretinal degeneration and retinal detachmentBenjamin M Nash, Christopher J G Watson, Edward Hughes, et al.
Stem Cells International|December 23, 2021
Evaluation for Retinal Therapy for <i>RPE65</i> Variation Assessed in hiPSC Retinal Pigment Epithelial CellsBenjamin M Nash, To Ha Loi, Milan Fernando, et al.
BMJ Open Ophthalmology|November 19, 2021
Efficient capture of high-quality real-world data on treatments for glaucoma: the Fight Glaucoma Blindness! RegistryMitchell Lawlor, Vuong Nguyen, Anne Brooks, et al.
Human Mutation|December 24, 2015
Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation SequencingAlan S Ma, John R Grigg, Gladys Ho, et al.
Human Mutation|May 12, 2007
Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocationRobyn V Jamieson, Nicola Farrar, Katrina Stewart, et al.
Translational Vision Science & Technology|May 20, 2022
Electrophysiological Assessment in Birdshot Chorioretinopathy: Flicker Electroretinograms Recorded With a Handheld DeviceAnna M Waldie, Angharad E Hobby, Isabelle Chow, et al.
BMJ Open|September 30, 2025
Australian research priorities for inherited retinal diseases: a James Lind Alliance priority setting partnershipEden G Robertson, Kate Hetherington, Meredith Prain, et al.
Pageof 15