D. Gilmour

发表

Incidence of submacular haemorrhage (SMH) in Scotland: a Scottish Ophthalmic Surveillance Unit (SOSU) study

D. Yorston, J. Hillenkamp, D. Steel, 2018, Eye.

Null mutations in LTBP2 cause primary congenital glaucoma.

D. Mackey, Shaheen N. Khan, S. Riazuddin, 2009, American journal of human genetics.

THE PENNSYLVANIA STATE UNIVERSITY SCHREYER HONORS COLLEGE DEPARTMENT OF BIOCHEMISTRY AND MOLECULAR BIOLOGY THE CONSTRUCTION OF ATAXIN-1 VECTORS FOR ANALYSIS OF ATAXIN-1 FUNCTION IN DEVELOPMENT OF SPINOCEREBELLAR ATAXIA TYPE 1

Y. Mao, S. Ades, D. Gilmour, 2013 .

Familial exudative vitreoretinopathy and DiGeorge syndrome: a new locus for familial exudative vitreoretinopathy on chromosome 22q11.2?

C. Inglehearn, C. Toomes, E. Sheridan, 2009, Ophthalmology.

Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR).

R. MacLaren, P. Sergouniotis, A. Webster, 2012, Investigative ophthalmology & visual science.

Trans-Orbital Intra-Cranial Air Gun Injury

B. Fleck, K. Ramaesh, D. Gilmour, 2003, European journal of ophthalmology.

Viscocanalostomy versus trabeculectomy for primary open angle glaucoma: 4-year prospective randomized clinical trial

J. Miles, D. Gilmour, H. Devonport, 2009, Eye.

Familial exudative vitreoretinopathy and related retinopathies

D. Gilmour, DF Gilmour, 2015, Eye.

Images in vascular medicine

M. Bailey, P. Coughlin, D. Scott, 2011, Vascular medicine.

Pre-treatment clinical features in central retinal vein occlusion that predict visual outcome following intravitreal ranibizumab

D. Young, D. Gilmour, Kerr Brogan, 2018, BMC Ophthalmology.

Photodynamic Therapy for Circumscribed Choroidal Haemangioma in a Scottish Cohort

A. Jamison, D. Gilmour, P. Cauchi, 2018, Ocular Oncology and Pathology.

Photodynamic and Anti- VEGF Therapy for Polypoidal Choroidal Vasculopathy - ‘Real World’ Outcomes in a Caucasian Population.

A. Jamison, D. Young, D. Gilmour, 2021, The Open Ophthalmology Journal.

The development and assessment of a self-perceived quality of vision questionnaire to test pseudophakic patients

P. Aspinall, N. Patton, D. Gilmour, 2004, Ophthalmic epidemiology.

Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.

D. Mackey, K. Hayashi, A. Markham, 2010, American journal of human genetics.

Reduced bone mineral density and hyaloid vasculature remnants in a consanguineous recessive FEVR family with a mutation in LRP5

C. Inglehearn, C. Toomes, A. Reddy, 2006, British Journal of Ophthalmology.

Anatomical and functional outcomes following switching from aflibercept to ranibizumab in neovascular age-related macular degeneration in Europe: SAFARI study

N. Eter, K. Balaskas, I. Pearce, 2019, British Journal of Ophthalmology.

A systematic review and meta-analysis of the effect of intravitreal VEGF inhibitors on cardiorenal outcomes

P. Mark, N. Lang, J. Lees, 2022, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Long-term prevalence of pseudophakic photic phenomena.

N. Patton, T. Aslam, B. Dhillon, 2007, American journal of ophthalmology-glaucoma.

THE PENNSYLVANIA STATE UNIVERSITY SCHREYER HONORS COLLEGE DEPARTMENT OF BIOCHEMISTRY AND MOLECULAR BIOLOGY A STUDY OF OKL38, A POTENTIAL TUMOR SUPPRESSOR, IN MITOCHONDRIA STRUCTURE AND FUNCTION

Jing Hu, Yanming Wang, A. Tokarski, 2011 .

Neuro-ophthalmology: examination and investigation

D. Gilmour, C. Lueck, G. Mcilwaine, 2004, Journal of Neurology, Neurosurgery & Psychiatry.