Zobrazeno 1 - 10
of 29
pro vyhledávání: '"James E. H. Smith"'
Publikováno v:
Case Reports in Ophthalmological Medicine, Vol 2018 (2018)
Purpose. To report the efficacy of subconjunctival triamcinolone (Kenalog A-40, Alcon) and bevacizumab (Avastin, Genentech) injections in fraternal twins with blepharokeratoconjunctivitis (BKC) causing progressive, bilateral corneal neovascularizatio
Externí odkaz:
https://doaj.org/article/a24a9bc03aac42b3a6f0e6090d542add
Autor:
Daniel Polya, Timothy V. Roberts, Samantha Fraser-Bell, Michael Mihail, James E. H. Smith, Tae Park, Noni L. Lewis, Fiona Stanaway, Andrew W. Kam, Scott Collins
Publikováno v:
BMC Health Services Research, Vol 21, Iss 1, Pp 1-9 (2021)
BMC Health Services Research
BMC Health Services Research
Background Increasing patient numbers, complexity of patient management, and healthcare resource limitations have resulted in prolonged patient wait times, decreased quality of service, and decreased patient satisfaction in many outpatient services w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98640e98b4b2ab28b97d890a5e3e73bc
https://doaj.org/article/7c5b18b8e72742cfa2e0a85b2704f3ca
https://doaj.org/article/7c5b18b8e72742cfa2e0a85b2704f3ca
Autor:
Lisa S. Kearns, Deepa A Taranath, Sandra E Staffieri, Angela J Chappell, Jillian Nicholl, James E. H. Smith, Emmanuelle Souzeau, Andrew Narita, Kathryn P. Burdon, James E. Elder, Tiger Zhou, Alex W. Hewitt, Jamie E Craig, Jonathan B Ruddle, David A. Mackey, Andrew Dubowsky, Shari Javadiyan, John Pater, Owen M. Siggs
Publikováno v:
Ophthalmology. 127:758-766
Developmental abnormalities of the ocular anterior segment in some cases can lead to ocular hypertension and glaucoma. CPAMD8 is a gene of unknown function recently associated with ocular anterior segment dysgenesis, myopia, and ectopia lentis. We so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f32e9ae1985f09ea21ffe7c3307e16b5
https://doi.org/10.1016/j.ophtha.2019.12.024
https://doi.org/10.1016/j.ophtha.2019.12.024
Autor:
Anna M. Waldie, Nicholas S. Little, Matti L Gild, Oliver Lau, Roderick J. Clifton-Bligh, James E. H. Smith, Mark Thieben, Janice Brewer
Publikováno v:
Neuroophthalmology
Lymphocytic hypophysitis (LYH) is a neuroendocrine disorder characterised by autoimmune inflammation of the pituitary gland with varying degrees of pituitary dysfunction, visual field defects and ocular motility disturbance. The authors report an int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::932694347c33044f398a68ad00c5f844
https://doi.org/10.1080/01658107.2018.1561721
https://doi.org/10.1080/01658107.2018.1561721
Autor:
Mark Y. Chiang, Glen A. Gole, Jamie E Craig, Lachlan S.W. Knight, Faren Willett, David A. Mackey, James E. H. Smith, Ayub Qassim, James Breen, Sandra E Staffieri, Guy D’Mellow, James E. Elder, Sean Mullany, Andrea L Vincent, Jonathan B Ruddle, Ivan Goldberg, Owen M. Siggs, Lisa S. Kearns, Susie Luu, Emmanuelle Souzeau, Deepa A Taranath
Publikováno v:
Ophthalmology. 128(11)
To report the relative frequencies of childhood and early onset glaucoma subtypes and their genetic findings in a large single cohort.Retrospective clinical and molecular study.All individuals with childhood glaucoma (diagnosed 0 to18 years) and earl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::942b8b5c884f66f28a4351a36e2c604e
https://pubmed.ncbi.nlm.nih.gov/33892047
https://pubmed.ncbi.nlm.nih.gov/33892047
Autor:
Peter McCluskey, Anthony J. Gill, Eugene Wong, Juliana Andrici, James E. H. Smith, Lawrence J. Oh
Publikováno v:
Internal Medicine Journal. 48:408-413
BACKGROUND Temporal artery biopsy is considered the investigation of choice to diagnose definitively giant cell arteritis (GCA) in patients with compatible symptoms. However it is invasive and not completely sensitive. Serum markers, particularly ery
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::794aebc3e5f0f28fc4901febf9d7e09a
https://doi.org/10.1111/imj.13713
https://doi.org/10.1111/imj.13713
Publikováno v:
Clinical & Experimental Ophthalmology. 46:702-705
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81d099db848583c1d0b625796d0b72d9
https://doi.org/10.1111/ceo.13161
https://doi.org/10.1111/ceo.13161
Autor:
Paul Giles, Emmanuelle Souzeau, Andrew Dubowsky, Lisa S. Kearns, Richard A. Mills, Jamie E Craig, Alex W. Hewitt, Trevor Hodson, Sandra E Staffieri, James E. H. Smith, Vivek Phakey, John Landers, James E. Elder, Owen M. Siggs, Tiger Zhou, Deepa A Taranath, Anna Galanopoulos, Jonathan B Ruddle, Kathryn P. Burdon, Julian L Rait, David A. Mackey, John Pater
Publikováno v:
European Journal of Human Genetics
Variation in FOXC1 and PITX2 is associated with Axenfeld-Rieger syndrome, characterised by structural defects of the anterior chamber of the eye and a range of systemic features. Approximately half of all affected individuals will develop glaucoma, b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::301542206ed9e5e37dd8a06e9276aa86
https://doi.org/10.1038/ejhg.2017.59
https://doi.org/10.1038/ejhg.2017.59
Publikováno v:
ANZ Journal of Surgery. 88:191-195
BACKGROUND Giant cell arteritis (GCA) is considered an ophthalmological emergency with severe sight and life-threatening sequelae. Temporal artery biopsy (TAB) is the current gold standard for the diagnosis of GCA; however, the required length of bio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::441a99e09785b5a683c4aae19901c255
https://doi.org/10.1111/ans.13822
https://doi.org/10.1111/ans.13822
Autor:
Clare L. Fraser, Frank A. Billson, Frank Martin, Anson Cheng, David Mowat, Bruce Bennetts, Robyn V. Jamieson, John R. Grigg, Katherine Holman, Alan Ma, Maree Flaherty, Elizabeth Farnsworth, Gladys Ho, James E. H. Smith, John Christodoulou, Ivan Prokudin
Publikováno v:
Human Mutation
Congenital cataracts are a significant cause of lifelong visual loss. They may be isolated or associated with microcornea, microphthalmia, anterior segment dysgenesis (ASD) and glaucoma, and there can be syndromic associations. Genetic diagnosis is c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e83471a6bb0c48f6587fd36e72631b1
https://doi.org/10.1002/humu.22948
https://doi.org/10.1002/humu.22948