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Robyn V Jamieson

Showing results (51-60 of 78) with videos related to

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Clinical Ophthalmology (Auckland, N.Z.)|August 7, 2023
Prevalence of Glaucoma Following Paediatric Cataract Surgery in an Australian Tertiary Referral CentreAlanna Wood, Benjamin Lim, Jim Matthews, et al.
Eye (London, England)|May 21, 2026
The quality-of-life impacts and economic burden of X-linked retinitis pigmentosa caused by variants in RPGRDeborah Schofield, Joshua Kraindler, Rupendra N Shrestha, et al.
Ophthalmic Genetics|July 22, 2021
<i>MERTK</i> retinopathy: biomarkers assessing vision lossDhimas H Sakti, Elisa E Cornish, Nina Mustafic, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 25, 2023
Early recognition of CLN3 disease facilitated by visual electrophysiology and multimodal imagingDhimas H Sakti, Elisa E Cornish, Clare L Fraser, 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.
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.
Pageof 8

Showing results (51-60 of 78) with videos related to

Sort By:
Pageof 8
Clinical Ophthalmology (Auckland, N.Z.)|August 7, 2023
Prevalence of Glaucoma Following Paediatric Cataract Surgery in an Australian Tertiary Referral CentreAlanna Wood, Benjamin Lim, Jim Matthews, et al.
Eye (London, England)|May 21, 2026
The quality-of-life impacts and economic burden of X-linked retinitis pigmentosa caused by variants in RPGRDeborah Schofield, Joshua Kraindler, Rupendra N Shrestha, et al.
Ophthalmic Genetics|July 22, 2021
<i>MERTK</i> retinopathy: biomarkers assessing vision lossDhimas H Sakti, Elisa E Cornish, Nina Mustafic, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 25, 2023
Early recognition of CLN3 disease facilitated by visual electrophysiology and multimodal imagingDhimas H Sakti, Elisa E Cornish, Clare L Fraser, 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.
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.
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