Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Colin J. Vize"'
Autor:
Tom H Williamson, D. A. Laidlaw, David Yorston, Abdallah A. Ellabban, Ajay D Patil, Edward Morris, Melanie Hingorani, Colin J Vize, Dilip B Patil
Publikováno v:
The Obstetrician & Gynaecologist. 22:217-226
Autor:
Ajay D Patil, Edward Morris, Colin J Vize, David Yorston, Abdallah A. Ellabban, Tom H Williamson, D. A. Laidlaw
Publikováno v:
The Obstetrician & Gynaecologist. 22:103-105
Publikováno v:
BMJ. :m569
Publikováno v:
European Ophthalmic Review. 12:105
Introduction:This proof-of-concept study aims to demonstrate that quantitative texture analysis of magnetic resonance imaging (MRI) of orbital tumours can produce a unique footprint as an adjunct to histology and as a reference guide.Methods:‘MaZda
Publikováno v:
Clinical & Experimental Ophthalmology. 41:609-611
Publikováno v:
Ophthalmic plastic and reconstructive surgery. 28(3)
PURPOSE To evaluate the effect of axial globe length and other biometry parameters on age-related lower eyelid malposition. METHODS Consecutive patients with involutional lower eyelid malposition underwent preoperative biometry with Zeiss IOL Master
Publikováno v:
Ophthalmic plastic and reconstructive surgery. 27(5)
Publikováno v:
British Journal of Ophthalmology. 84:429-431
AIMS—To determine whether there were any specific factors that influenced waiting list time (WLT) for patients undergoing cataract surgery. METHODS—70 preoperative cataract patients were interviewed by one of the authors using a questionnaire to
Autor:
Ruth Newbury-Ecob, NJ Marchbank, Graeme C.M. Black, Masoud Teimory, Alexander F. Markham, Colin J. Vize, Nishal Patel, David A. Mackey, Amanda J. Churchill, Chris F. Inglehearn, Christopher P. Bennett, Carmel Toomes, Shrivatsa P. Desai, Jamie E Craig
Publikováno v:
Scopus-Elsevier
Flinders University PURE
University of Western Australia
Flinders University PURE
University of Western Australia
Dominant optic atrophy (DOA) is the commonest form of inherited optic neuropathy. Although heterogeneous, a major locus has been mapped to chromosome 3q28 and the gene responsible, OPA1, was recently identified. We therefore screened a panel of 35 DO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62cd0452c77d1393f1929f0115570155
http://www.scopus.com/inward/record.url?eid=2-s2.0-0035875096&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0035875096&partnerID=MN8TOARS