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R Grigg

Showing results (121-130 of 150) with videos related to

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American Journal of Ophthalmology|January 31, 2015
Primary congenital glaucoma outcomes: lessons from 23 years of follow-upSophia L Zagora, Charlotte L Funnell, Frank J Martin, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 6, 2018
Monitoring of optic nerve function in Neurofibromatosis 2 children with optic nerve sheath meningiomas using multifocal visual evoked potentialsV Jayanetti, A I Klistorner, S L Graham, et al.
Journal of Personalized Medicine|March 25, 2022
Human iPSC-Derived Retinal Organoids and Retinal Pigment Epithelium for Novel Intronic <i>RPGR</i> Variant Assessment for Therapy SuitabilityFidelle Chahine Karam, To Ha Loi, Alan Ma, et al.
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.
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.
Pageof 15

Showing results (121-130 of 150) with videos related to

Sort By:
Pageof 15
American Journal of Ophthalmology|January 31, 2015
Primary congenital glaucoma outcomes: lessons from 23 years of follow-upSophia L Zagora, Charlotte L Funnell, Frank J Martin, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 6, 2018
Monitoring of optic nerve function in Neurofibromatosis 2 children with optic nerve sheath meningiomas using multifocal visual evoked potentialsV Jayanetti, A I Klistorner, S L Graham, et al.
Journal of Personalized Medicine|March 25, 2022
Human iPSC-Derived Retinal Organoids and Retinal Pigment Epithelium for Novel Intronic <i>RPGR</i> Variant Assessment for Therapy SuitabilityFidelle Chahine Karam, To Ha Loi, Alan Ma, et al.
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.
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.
Pageof 15