Zobrazeno 1 - 10
of 182
pro vyhledávání: '"Anthony G Robson"'
Publikováno v:
PLoS ONE, Vol 14, Iss 5, p e0217265 (2019)
It has been postulated that particular patterns of macular pigment (MP) distribution may be associated with the risk for eye diseases such as age-related macular degeneration (AMD). This work investigates the potential of Zernike polynomials (ZP) to
Externí odkaz:
https://doaj.org/article/ac7cdcd4be37441295de4878e9a8f099
Autor:
Mei Hong Tan, Donna S Mackay, Jill Cowing, Hoai Viet Tran, Alexander J Smith, Genevieve A Wright, Arundhati Dev-Borman, Robert H Henderson, Phillip Moradi, Isabelle Russell-Eggitt, Robert E MacLaren, Anthony G Robson, Michael E Cheetham, Dorothy A Thompson, Andrew R Webster, Michel Michaelides, Robin R Ali, Anthony T Moore
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e32330 (2012)
Leber Congenital Amaurosis (LCA) and Early Childhood Onset Severe Retinal Dystrophy are clinically and genetically heterogeneous retinal disorders characterised by visual impairment and nystagmus from birth or early infancy. We investigated the preva
Externí odkaz:
https://doaj.org/article/ab358eecd7e74aa495b458512900acef
Autor:
Rola Ba-Abbad, Graham E. Holder, Anthony G. Robson, Magella M. Neveu, Naushin Waseem, Gavin Arno, Andrew R. Webster
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 14, Iss , Pp 83-86 (2019)
Purpose: To describe the clinical and electrophysiological features of an unusual retinopathy in a patient with a novel genotype of CNGB1, mutations in which are implicated in autosomal recessive retinitis pigmentosa (rod-cone dystrophy). Observation
Externí odkaz:
https://doaj.org/article/5f6c263b7d5a4a3ea91eb01636e85545
Autor:
Michalis Georgiou, Anthony G. Robson, Katarina Jovanovic, Thales A. C. de Guimarães, Naser Ali, Nikolas Pontikos, Sami H. Uwaydat, Omar A. Mahroo, Michael E. Cheetham, Andrew R. Webster, Alison J. Hardcastle, Michel Michaelides
Publikováno v:
Ophthalmology. 130:413-422
Publikováno v:
Ophthalmic Genetics. :1-6
Autor:
Michel Michaelides, Nashila Hirji, Sui Chien Wong, Cagri G. Besirli, Serena Zaman, Neruban Kumaran, Anastasios Georgiadis, Alexander J. Smith, Caterina Ripamonti, Irene Gottlob, Anthony G. Robson, Alberta Thiadens, Robert H. Henderson, Penny Fleck, Eddy Anglade, Xiangwen Dong, George Capuano, Wentao Lu, Pamela Berry, Thomas Kane, Stuart Naylor, Michalis Georgiou, Angelos Kalitzeos, Robin R. Ali, Alexandria Forbes, James Bainbridge
Publikováno v:
American Journal of Ophthalmology.
Publikováno v:
RETINAL Cases & Brief Reports. 16:507-510
PURPOSE To demonstrate phenotypic discordance between a monozygotic twin pair, one of whom exhibited pigmented paravenous chorioretinal atrophy (PPCRA). METHODS A patient and his identical twin brother, attending Moorfields Eye Hospital, were reviewe
Autor:
Magella M Neveu, Srikanta Kumar Padhy, Srishti Ramamurthy, Brijesh Takkar, Subhadra Jalali, Deepika CP, Tapas Ranjan Padhi, Anthony G Robson
Publikováno v:
Clinical Ophthalmology. 16:1569-1587
Albinism describes a heterogeneous group of genetically determined disorders characterized by disrupted synthesis of melanin and a range of developmental ocular abnormalities. The main ocular features common to both oculocutaneous albinism (OCA), and
Autor:
Kazushige Tsunoda, Camiel J. F. Boon, Ester Carreño, Xiao Liu, Rachel M. Huckfeldt, Mark E. Pennesi, Andrew R. Webster, Anthony G. Robson, Elise Héon, Gavin Arno, Susanne Kohl, Belen Jimenez-Rolando, Michel Michaelides, Carmen Ayuso, Omar A. Mahroo, Eyal Banin, Samer Khateb, Takaaki Hayashi, Bernd Wissinger, Arif O. Khan, Eberhart Zrenner, Alberta A H J Thiadens, Ajoy Vincent, Nikolas Pontikos, Maria Inmaculada Martin-Merida, Thales Antonio Cabral de Guimaraes, Xuan-Thanh-An Nguyen, Michalis Georgiou, Almudena Avila-Fernandez, Mauricio E Vargas, Emanuel R. de Carvalho, Shaun Michael Leo, Yu Fujinami-Yokokawa, Dror Sharon, Fadi Nasser, Kaoru Fujinami, Blanca Garcia-Sandoval
Publikováno v:
American journal of ophthalmology, 230, 1-11. Elsevier USA
American Journal of Ophthalmology, 230, 1-11. Elsevier Inc.
American Journal of Ophthalmology, 230. ELSEVIER SCIENCE INC
American Journal of Ophthalmology
American Journal of Ophthalmology, 230, 1-11. Elsevier Inc.
American Journal of Ophthalmology, 230. ELSEVIER SCIENCE INC
American Journal of Ophthalmology
Highlights • KCNV2-associated retinopathy is a slowly progressive disease with early retinal changes, which are predominantly symmetric between eyes. • Disease course can be unpredictable and may severely affect children and young adults. • Fin
Autor:
Sophie L. Glinton, Antonio Calcagni, Watjana Lilaonitkul, Nikolas Pontikos, Sandra Vermeirsch, Gongyu Zhang, Gavin Arno, Siegfried K. Wagner, Michel Michaelides, Pearse A. Keane, Andrew R. Webster, Omar A. Mahroo, Anthony G. Robson
Publikováno v:
Translational vision sciencetechnology. 11(9)
Biallelic pathogenic variants in ABCA4 are the commonest cause of monogenic retinal disease. The full-field electroretinogram (ERG) quantifies severity of retinal dysfunction. We explored application of machine learning in ERG interpretation and in g