Zobrazeno 1 - 10
of 124
pro vyhledávání: '"Glen A. Gole"'
Autor:
Thomas P. Moloney, Glen A. Gole
Publikováno v:
Case Reports in Ophthalmology, Vol 13, Iss 2, Pp 382-384 (2022)
Stickler syndrome is one of the most common inherited causes of retinal detachment in childhood. We present the case of a 6-year-old boy with Stickler syndrome who developed a retinal detachment in his better seeing eye after prolonged trampoline use
Externí odkaz:
https://doaj.org/article/b0bd88a4f8c84eaaa05f27715637d7df
Publikováno v:
Clinicalexperimental optometry.
Collaboration between hospital-based ophthalmology and community-based optometry could pave the way to improve access to paediatric eyecare services.The Paediatric Optometry Alignment Program (POAP) began in 2016 as a proof-of-concept pilot project t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b781058003b5a3605c29b5e455c11e39
https://pubmed.ncbi.nlm.nih.gov/36417949
https://pubmed.ncbi.nlm.nih.gov/36417949
Publikováno v:
Australian Journal of General Practice. 49:815-822
Background Acute red eye in a child is a common ocular presentation in general practice. It can arise from a wide spectrum of pathologies and involve various ocular structures. Objective The aim of this article is to provide a framework for the gener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e3a3ec6ac4a6dead28b1991ae5c059
https://doi.org/10.31128/ajgp-02-20-5240
https://doi.org/10.31128/ajgp-02-20-5240
Publikováno v:
Clinical & Experimental Ophthalmology. 48:879-888
Importance: Indigenous communities of Far North Queensland (FNQ) have one of the highest incidences of alcohol-related ocular trauma globally. Background: To review the epidemiology of closed- and open-globe trauma admitted to Cairns Hospital from FN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa2eeec66f4c2fa8c0693c602cb06454
https://doi.org/10.1111/ceo.13811
https://doi.org/10.1111/ceo.13811
Publikováno v:
Ophthalmic epidemiology. 29(4)
Background Children's vision screening children commonly uses optotype-based visual acuity or instrument-based methods measuring amblyogenic risk factors (ARFs). Objective To compare the performance of the Spot Vision Screener (SVS) (PediaVision, Wel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0db6dfd848fb0feeea918891959e0523
https://pubmed.ncbi.nlm.nih.gov/34423736
https://pubmed.ncbi.nlm.nih.gov/34423736
Autor:
David Coman, Jaak Jaeken, Vanessa dos Reis Ferreira, Dorinda Marques-da-Silva, Carlota Pascoal, Eva Morava, Glen A. Gole, Rita Francisco
Publikováno v:
Journal of Inherited Metabolic Disease. 42:29-48
Congenital disorders of glycosylation (CDG) are a rapidly growing family comprising >100 genetic diseases. Some 25 CDG are pure O-glycosylation defects. Even among this CDG subgroup, phenotypic diversity is broad, ranging from mild to severe poly-org
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c819b68aeaed37c70544bfc50dfbf515
https://doi.org/10.1002/jimd.12025
https://doi.org/10.1002/jimd.12025
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
Publikováno v:
Case Reports in Genetics, Vol 2018 (2018)
Case Reports in Genetics
Case Reports in Genetics
Hajdu-Cheney Syndrome (HSC) is a rare multisystem disease in which the phenotype involves acro-osteolysis, severe osteoporosis, short stature, wormian bones, facial dysmorphism, central neurological abnormalities, cardiovascular defects, and polycyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ea42a0d602a1feea19e60dc96c09850
https://doi.org/10.1155/2018/2508345
https://doi.org/10.1155/2018/2508345
Publikováno v:
Clinical & Experimental Ophthalmology. 46:645-651
Demand for Retinopathy of Prematurity screening, is increasing for infants born at rural and regional hospitals where the service is not generally available. The health system cost for screening regional/remote infants has not been reported. The obje
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ba0969966e69adaa0492844ff85d887
https://doi.org/10.1111/ceo.13160
https://doi.org/10.1111/ceo.13160
Publikováno v:
Journal of Telemedicine and Telecare. 25:106-122
The objective of this review was to identify and describe telehealth models of care for ophthalmic services. We conducted a scoping review of the literature to identify how ophthalmic care can be delivered by telehealth. We searched the PubMed databa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c50a09c66a2fae0d5f66bac55b49655c
https://doi.org/10.1177/1357633x17742182
https://doi.org/10.1177/1357633x17742182