Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Mary S. Attia"'
Autor:
Bert C. Giers, Ramin Khoramnia, Dorottya Varadi, Hannah Wallek, Hyeck-Soo Son, Mary S. Attia, Gerd U. Auffarth
Publikováno v:
BMC Ophthalmology, Vol 19, Iss 1, Pp 1-9 (2019)
Abstract Background Evaluation of clinical and functional results of a new extended depth of focus intraocular lens (EDOF-IOL). Methods Fourteen cataract patients (28 bilateral implantations) were assessed for uncorrected (UDVA) and corrected (CDVA)
Externí odkaz:
https://doaj.org/article/7fbccf604c1945f1aa99d75a0a9fa6c9
Autor:
Samuel McLenachan, Dan Zhang, Janya Grainok, Xiao Zhang, Zhiqin Huang, Shang-Chih Chen, Khine Zaw, Alanis Lima, Luke Jennings, Danial Roshandel, Sang Yoon Moon, Rachael C. Heath Jeffery, Mary S. Attia, Jennifer A. Thompson, Tina M. Lamey, Terri L. McLaren, John De Roach, Sue Fletcher, Fred K. Chen
Publikováno v:
Genes, Vol 12, Iss 10, p 1542 (2021)
Retinitis pigmentosa 11 (RP11) is caused by dominant mutations in PRPF31, however a significant proportion of mutation carriers do not develop retinopathy. Here, we investigated the relationship between CNOT3 polymorphism, MSR1 repeat copy number and
Externí odkaz:
https://doaj.org/article/0433099566284270920937d1a1ac0465
Autor:
Jason Charng, Chandrakumar Balaratnasingam, Mary S. Attia, Rachael C. Heath Jeffery, Fred K. Chen
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 260:2157-2164
Purpose To investigate retinal sensitivity changes in eyes with pure cuticular drusen. Methods Multimodal imaging and microperimetry (37-loci grid) data were examined retrospectively to evaluate functional changes in eyes with pure cuticular drusen.
Autor:
Enid Chelva, Dan Zhang, Jason Charng, David A. Mackey, Jennifer A. Thompson, Tina M. Lamey, Sue Fletcher, Terri L. McLaren, Mary S. Attia, Danial Roshandel, Sukanya Arunachalam, John N. De Roach, Steve D. Wilton, Samuel McLenachan, Fred K. Chen
Publikováno v:
Ophthalmic Genetics. 42:1-14
Mutations in the splicing factor pre-messenger RNA processing factor 31 (PRPF31) gene cause autosomal dominant retinitis pigmentosa 11 (RP11) through a haplo-insufficiency mechanism. We describe th...
Autor:
Di Huang, Jennifer A. Thompson, Shang-Chih Chen, Abbie Adams, Ianthe Pitout, Alanis Lima, Dan Zhang, Rachael C. Heath Jeffery, Mary S. Attia, Terri L. McLaren, Tina M. Lamey, John N. De Roach, Samuel McLenachan, May Thandar Aung-Htut, Sue Fletcher, Steve D. Wilton, Fred K. Chen
Publikováno v:
SSRN Electronic Journal.
The ATP-binding cassette subfamily A member 4 gene (ABCA4)-associated retinopathy, Stargardt disease, is the most common monogenic inherited retinal disease. Given the pathogenicity of numerous ABCA4 variants is yet to be examined and a significant p
Autor:
Michael Millward, Sanjeevan Muruganandan, Wei Sen Lam, J. Spiro, Sukanya Arunachalam, Aron Chakera, Y. C. Gary Lee, Catherine A. Read, Mary S. Attia, Anna K. Nowak, Fred K. Chen, Wee Loong Chin, Kevin Murray, Jenette Creaney
Publikováno v:
Lung Cancer. 140:87-92
Objectives Currently, there is no optimal salvage therapy for patients with malignant pleural mesothelioma (MPM) who relapse after treatment with first-line chemotherapy. In line with the strong preclinical rationale for targeting fibroblast growth f
Autor:
Zhiqin Huang, Dan Zhang, Jennifer A. Thompson, Alanis Lima, Shang Chih Chen, Tina M. Lamey, Sue Fletcher, Sang Yoon Moon, Mary S. Attia, Xiao Zhang, Khine Zaw, Janya Grainok, John N. De Roach, Terri L. McLaren, Fred K. Chen, Luke Jennings, Danial Roshandel, Samuel McLenachan, Rachael C. Heath Jeffery
Publikováno v:
Genes
Volume 12
Issue 10
Genes, Vol 12, Iss 1542, p 1542 (2021)
Volume 12
Issue 10
Genes, Vol 12, Iss 1542, p 1542 (2021)
Retinitis pigmentosa 11 (RP11) is caused by dominant mutations in PRPF31, however a significant proportion of mutation carriers do not develop retinopathy. Here, we investigated the relationship between CNOT3 polymorphism, MSR1 repeat copy number and
Autor:
Michael Millward, Mary S. Attia, Sanjeevan Muruganandan, Fred K. Chen, Catherine A. Read, J. Spiro, Wei-Sen Lam, Anna K. Nowak, Jenette Creaney, Sukanya Arunachalam, Y. C. Gary Lee, Aron Chakera, Jason Charng
Publikováno v:
Clinicalexperimental ophthalmologyREFERENCES. 49(6)
Background To describe ocular adverse events and retinal changes during fibroblast growth factor receptor (FGFR) inhibitor (AZD4547) anticancer therapy. Methods This is a sub-study examining ocular adverse effects from AZD4547 therapy (single-centre,
Autor:
Jason Charng, Di Xiao, John N. De Roach, Tina M. Lamey, Fred K. Chen, Sukanya Arunachalam, Jennifer A. Thompson, David A. Mackey, Mary S. Attia, Shaun Frost, Terri L. McLaren, Maryam Mehdizadeh
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Scientific Reports
Scientific Reports
Stargardt disease is one of the most common forms of inherited retinal disease and leads to permanent vision loss. A diagnostic feature of the disease is retinal flecks, which appear hyperautofluorescent in fundus autofluorescence (FAF) imaging. The
Autor:
Danial, Roshandel, Jennifer A, Thompson, Jason, Charng, Dan, Zhang, Enid, Chelva, Sukanya, Arunachalam, Mary S, Attia, Tina M, Lamey, Terri L, McLaren, John N, De Roach, David A, Mackey, Steve D, Wilton, Sue, Fletcher, Samuel, McLenachan, Fred K, Chen
Publikováno v:
Ophthalmic genetics. 42(1)
Mutations in the splicing factor pre-messenger RNA processing factor 31 (Ophthalmic examination, optical coherence tomography, fundus autofluorescence and microperimetry were performed at baseline and every 6-12 months. Baseline and annual change in