Zobrazeno 1 - 10
of 145
pro vyhledávání: '"John R. Grigg"'
Publikováno v:
Clinical Case Reports, Vol 11, Iss 12, Pp n/a-n/a (2023)
Key Clinical Message Inherited retinal dystrophies typically affect vision in early childhood; however, this case highlights a late onset retinal dystrophy presenting in midlife and the need for extended visual electrophysiology testing to determine
Externí odkaz:
https://doaj.org/article/7812274ff2b7458d9ca3bc5336194e92
Autor:
Matthew J. G. Watson, Peter J. McCluskey, John R. Grigg, Yogesan Kanagasingam, Judith Daire, Mohamed Estai
Publikováno v:
BMC Family Practice, Vol 22, Iss 1, Pp 1-10 (2021)
Abstract Background Despite recent incentives through Medicare (Australia’s universal health insurance scheme) to increase retinal screening rates in primary care, comprehensive diabetic retinopathy (DR) screening has not been reached in Australia.
Externí odkaz:
https://doaj.org/article/deb0ad8a4b36462290a30ed2974a002f
Autor:
Samuel C. Eggenberger, Natalie L. James, Cherry Ho, Steven S. Eamegdool, Veronika Tatarinoff, Naomi A. Craig, Barry S. Gow, Susan Wan, Christopher W.D. Dodds, Donna La Hood, Aaron Gilmour, Shannon L. Donahoe, Mark Krockenberger, Krishna Tumuluri, Melville J. da Cruz, John R. Grigg, Peter McCluskey, Nigel H. Lovell, Michele C. Madigan, Adrian T. Fung, Gregg J. Suaning
Publikováno v:
Data in Brief, Vol 39, Iss , Pp 107634- (2021)
The data presented here are related and supplementary data to the research article “Implantation and long-term assessment of the stability and biocompatibility of a novel 98 channel suprachoroidal visual prosthesis in sheep” [1]. In Eggenberger e
Externí odkaz:
https://doaj.org/article/63829d9e51c44b09b0e506d4d9a1d8d7
Autor:
Benjamin M. Nash, To Ha Loi, Milan Fernando, Amin Sabri, James Robinson, Anson Cheng, Steven S. Eamegdool, Elizabeth Farnsworth, Bruce Bennetts, John R. Grigg, Seo-Kyung Chung, Anai Gonzalez-Cordero, Robyn V. Jamieson
Publikováno v:
Stem Cells International, Vol 2021 (2021)
Human induced pluripotent stem cells (hiPSCs) generated from patients and the derivative retinal cells enable the investigation of pathological and novel variants in relevant cell populations. Biallelic pathogenic variants in RPE65 cause early-onset
Externí odkaz:
https://doaj.org/article/efc0b3e3faab4cc08d30e555d2e914e1
Autor:
Benjamin M. Nash, Alan Ma, Gladys Ho, Elizabeth Farnsworth, Andre E. Minoche, Mark J. Cowley, Christopher Barnett, Janine M. Smith, To Ha Loi, Karen Wong, Luke St Heaps, Dale Wright, Marcel E. Dinger, Bruce Bennetts, John R. Grigg, Robyn V. Jamieson
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 7, p 3905 (2022)
The inherited retinal dystrophies (IRDs) are a clinically and genetically complex group of disorders primarily affecting the rod and cone photoreceptors or other retinal neuronal layers, with emerging therapies heralding the need for accurate molecul
Externí odkaz:
https://doaj.org/article/0cebdd4d5ce8417199fe976e77ef071a
Autor:
Fidelle Chahine Karam, To Ha Loi, Alan Ma, Benjamin M. Nash, John R. Grigg, Darshan Parekh, Lisa G. Riley, Elizabeth Farnsworth, Bruce Bennetts, Anai Gonzalez-Cordero, Robyn V. Jamieson
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 3, p 502 (2022)
The RPGR gene encodes Retinitis Pigmentosa GTPase Regulator, a known interactor with ciliary proteins, which is involved in maintaining healthy photoreceptor cells. Variants in RPGR are the main contributor to X-linked rod-cone dystrophy (RCD), and R
Externí odkaz:
https://doaj.org/article/bd10374474d04ff3ad319d610201f24e
Publikováno v:
International Journal of Retina and Vitreous, Vol 4, Iss 1, Pp 1-5 (2018)
Abstract Background Macular holes in children are generally associated with trauma. Case presentation We report the first case of an idiopathic full thickness macular hole in a 10-year-old girl. 23-gauge transconjunctival pars plana vitrectomy, induc
Externí odkaz:
https://doaj.org/article/87fea2fea3964447bc9d55a5c3d75196
Survey of perspectives of people with inherited retinal diseases on ocular gene therapy in Australia
Autor:
Heather G. Mack, Alexis Ceecee Britten-Jones, Myra B. McGuinness, Fred K. Chen, John R. Grigg, Robyn V. Jamieson, Thomas L. Edwards, John De Roach, Fleur O’Hare, Keith R. Martin, Lauren N. Ayton
Publikováno v:
Gene Therapy. 30:336-346
Many gene therapies are in development for treating people with inherited retinal diseases (IRD). We hypothesized that potential recipients of gene therapy would have knowledge gaps regarding treatment. We aimed to assess knowledge, attitudes, and pe
Publikováno v:
Clinical & Experimental Ophthalmology.
Autor:
Dhimas H. Sakti, Elisa E. Cornish, Clare L. Fraser, Benjamin M. Nash, Trent M. Sandercoe, Michael M. Jones, Neil A. Rowe, Robyn V. Jamieson, Alexandra M. Johnson, John R. Grigg
Publikováno v:
Documenta Ophthalmologica.
Background Neuronal ceroid lipofuscinosis is a group of neurodegenerative disorders with varying visual dysfunction. CLN3 is a subtype which commonly presents with visual decline. Visual symptomatology can be indistinct making early diagnosis difficu