Zobrazeno 1 - 10
of 81
pro vyhledávání: '"D. J. Coster"'
Autor:
D. J. Coster, K. A. Williams
Allograft rejection is the major obstacle to successful corneal transplantation in high-risk cases. The risk factors are well recognized. Within the high-risk group, surgeons can influence graft survival by MHC antigen matching, by immunosuppression,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a79db56b9fdf93441ae89a2ac398e417
https://doi.org/10.1159/000417108
https://doi.org/10.1159/000417108
Autor:
Bruce C.V. Campbell, Keryn A. Williams, Andrew Lee, Celia S. Chen, John R. Grigg, Mark Paine, Tien Lee, Romesh Markus, D. J. Coster, Clare L. Fraser
Publikováno v:
International Journal of Stroke. 6:87-89
Rationale Central retinal artery occlusion is a stroke of the eye caused by a blockage of its main blood supply by platelet-fibrin clot. Systemic thrombolysis has been successful in restoring perfusion to ischaemic tissue by fibrin-platelet clot lysi
Autor:
Layal Abi Farraj, D. J. Coster, Ha Ae Bae, Judith Lechner, Paul Mitchell, Manir Ali, Maurice Yap, Gowthaman Govindarajan, Emmanuelle Souzeau, David Simpson, Richard A. Mills, Manoranjan Das, Colin E. Willoughby, Jasenka Guduric-Fuchs, Tony Phillips, Kathryn P. Burdon, Shea Ping Yip, Jamie E Craig, Salina Siddiqui, Richard G Lindsay, Periasamy Sundaresan, Chris F. Inglehearn, Aine Rice
Publikováno v:
Lechner, J, Bae, H A, Guduric-Fuchs, J, Rice, A, Govindarajan, G, Siddiqui, S, Abi Farraj, L, Yip, S P, Yap, M, Das, M, Souzeau, E, Coster, D, Mills, R A, Lindsay, R, Phillips, T, Mitchell, P, Ali, M, Inglehearn, C F, Sundaresan, P, Craig, J E, Simpson, D A, Burdon, K P & Willoughby, C E 2013, ' Mutational Analysis of MIR184 in Sporadic Keratoconus and Myopia ', Investigative Opthalmology and Visual Science, vol. 54, no. 8, pp. 5266-72 . https://doi.org/10.1167/iovs.13-12035
Author version made available in accordance with the publisher's policy.
A mutation miR-184(+57C>T) in the seed region of miR-184 (encoded by MIR184 [MIM*613146]) results in familial severe keratoconus combined with early-onset anterior polar ca
A mutation miR-184(+57C>T) in the seed region of miR-184 (encoded by MIR184 [MIM*613146]) results in familial severe keratoconus combined with early-onset anterior polar ca
Publikováno v:
British Journal of Ophthalmology. 80:256-262
AIMS: To examine factors influencing the density and contact inhibition of bovine corneal endothelial cells cultured in vitro. METHODS: Cell counts were performed on bovine corneal endothelial cells cultured for various times in the presence of 10% f
Publikováno v:
Cornea. 11:211-220
Publikováno v:
American Journal of Ophthalmology. 110:635-640
Methyl ethyl ketone peroxide is a commonly used catalyst in various industries. We studied 19 eyes with a single exposure to methyl ethyl ketone peroxide that developed clinical patterns of mild injury, moderate injury, severe injury, or delayed kera
Publikováno v:
Australian and New Zealand Journal of Ophthalmology. 18:155-158
A 48-year-old woman developed a crystalline stromal lesion four years after a penetrating corneal graft, with few signs of ocular inflammation. An initial diagnosis of fungal keratitis was made because of the appearance of the lesion. An excisional b
Publikováno v:
Transplantation. 71(9)
Modification of a donor cornea by gene therapy ex vivo has potential to modulate irreversible rejection, the major cause of corneal graft failure. Our aim was to transfer the gene encoding mammalian IL-10 to ovine donor corneas and to determine subse
Publikováno v:
Ophthalmology. 107(6)
To determine the long-term effect on vision of penetrating keratoplasty performed for keratoconus.Retrospective noncomparative case series.All patients with keratoconus who received a corneal graft and who remained in our center for follow-up and vis
Publikováno v:
Australian and New Zealand journal of ophthalmology. 27(6)
A case of linear IgA disease is reported to alert ophthalmologists and physicians to this unusual cause of chronic cicatrizing conjunctivitis.Clinical records of a patient suffering from linear IgA disease were reviewed.A 65-year-old woman with a com