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John R Grigg

Showing results (71-80 of 92) with videos related to

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Documenta Ophthalmologica. Advances in Ophthalmology|June 28, 2025
Detecting congenital chiasmal misrouting using multichannel VEPs: protocol for a scoping reviewGiulia Steuernagel Del Valle, Haipha Ali, John R Grigg, et al.
Retinal Cases & Brief Reports|July 6, 2019
UVEITIS CAUSED BY TREATMENT FOR MALIGNANT MELANOMA: A CASE SERIESEline Whist, Richard J Symes, John H Chang, et al.
European Journal of Human Genetics : EJHG|May 28, 2009
Novel SOX2 partner-factor domain mutation in a four-generation familyMarija Mihelec, Peter Abraham, Kate Gibson, et al.
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.
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.
Pageof 10

Showing results (71-80 of 92) with videos related to

Sort By:
Pageof 10
Documenta Ophthalmologica. Advances in Ophthalmology|June 28, 2025
Detecting congenital chiasmal misrouting using multichannel VEPs: protocol for a scoping reviewGiulia Steuernagel Del Valle, Haipha Ali, John R Grigg, et al.
Retinal Cases & Brief Reports|July 6, 2019
UVEITIS CAUSED BY TREATMENT FOR MALIGNANT MELANOMA: A CASE SERIESEline Whist, Richard J Symes, John H Chang, et al.
European Journal of Human Genetics : EJHG|May 28, 2009
Novel SOX2 partner-factor domain mutation in a four-generation familyMarija Mihelec, Peter Abraham, Kate Gibson, et al.
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.
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.
Pageof 10