Search research articles
Contact Us
Filters
Showing results (21-30 of 31) with videos related to
Page
of 4
Sort By:
Frontiers in Bioengineering and Biotechnology
|
March 15, 2017
Synergy Repetition Training versus Task Repetition Training in Acquiring New Skill
Vrajeshri Patel, Jamie Craig, Michelle Schumacher, et al.
Ophthalmology
|
January 5, 2005
Intravitreal triamcinolone-induced elevated intraocular pressure is associated with the development of posterior subcapsular cataract
Mark C Gillies, Maciek Kuzniarz, Jamie Craig, et al.
Clinical & Experimental Ophthalmology
|
October 2, 2015
Role of the nucleolus in neurodegenerative diseases with particular reference to the retina: a review
Paul I Sia, John Pm Wood, Glyn Chidlow, et al.
Human Genetics
|
May 21, 2005
Evidence for a novel glaucoma locus at chromosome 3p21-22
Paul N Baird, Simon J Foote, David A Mackey, et al.
Clinical & Experimental Ophthalmology
|
March 6, 2026
Incidence, Progression and Determinants of Diabetic Retinopathy in Type 2 Diabetes in Australasia: A Systematic Review and Meta-Analysis
Getasew Alemu Mersha, Mesert Derbew Molla, Ranjay Chakraborty, et al.
Journal of Clinical Immunology
|
January 27, 2022
Clinical Outcome and Underlying Genetic Cause of Functional Terminal Complement Pathway Deficiencies in a Multicenter UK Cohort
Annalie Shears, Cathal Steele, Jamie Craig, et al.
Clinical & Experimental Ophthalmology
|
July 7, 2022
Quantification of localised vascular wedge-shaped defects in glaucoma
Danit Saks, Angela Schulz, Samran Sheriff, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)
|
December 31, 2015
Causes of Severe Visual Impairment and Blindness: Comparative Data From Bhutanese and Laotian Schools for the Blind
Lachlan David Mailey Farmer, Soo Khai Ng, Adam Rudkin, et al.
American Journal of Human Genetics
|
April 14, 2009
Null mutations in LTBP2 cause primary congenital glaucoma
Manir Ali, Martin McKibbin, Adam Booth, et al.
Plos Genetics
|
May 12, 2021
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Hannah Currant, Pirro Hysi, Tomas W Fitzgerald, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Frontiers in Bioengineering and Biotechnology
|
March 15, 2017
Synergy Repetition Training versus Task Repetition Training in Acquiring New Skill
Vrajeshri Patel, Jamie Craig, Michelle Schumacher, et al.
Ophthalmology
|
January 5, 2005
Intravitreal triamcinolone-induced elevated intraocular pressure is associated with the development of posterior subcapsular cataract
Mark C Gillies, Maciek Kuzniarz, Jamie Craig, et al.
Clinical & Experimental Ophthalmology
|
October 2, 2015
Role of the nucleolus in neurodegenerative diseases with particular reference to the retina: a review
Paul I Sia, John Pm Wood, Glyn Chidlow, et al.
Human Genetics
|
May 21, 2005
Evidence for a novel glaucoma locus at chromosome 3p21-22
Paul N Baird, Simon J Foote, David A Mackey, et al.
Clinical & Experimental Ophthalmology
|
March 6, 2026
Incidence, Progression and Determinants of Diabetic Retinopathy in Type 2 Diabetes in Australasia: A Systematic Review and Meta-Analysis
Getasew Alemu Mersha, Mesert Derbew Molla, Ranjay Chakraborty, et al.
Journal of Clinical Immunology
|
January 27, 2022
Clinical Outcome and Underlying Genetic Cause of Functional Terminal Complement Pathway Deficiencies in a Multicenter UK Cohort
Annalie Shears, Cathal Steele, Jamie Craig, et al.
Clinical & Experimental Ophthalmology
|
July 7, 2022
Quantification of localised vascular wedge-shaped defects in glaucoma
Danit Saks, Angela Schulz, Samran Sheriff, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)
|
December 31, 2015
Causes of Severe Visual Impairment and Blindness: Comparative Data From Bhutanese and Laotian Schools for the Blind
Lachlan David Mailey Farmer, Soo Khai Ng, Adam Rudkin, et al.
American Journal of Human Genetics
|
April 14, 2009
Null mutations in LTBP2 cause primary congenital glaucoma
Manir Ali, Martin McKibbin, Adam Booth, et al.
Plos Genetics
|
May 12, 2021
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
Hannah Currant, Pirro Hysi, Tomas W Fitzgerald, et al.
Page
of 4