British Council for Prevention of Blindness Grant Programme 2019
The British Council for Prevention of Blindness supports research into the prevention of blindness in low and low-middle income countries throughout the world. Their latest round of grant funding for 2019 is now open. Grants are offered for research projects that further the goals of ‘VISION 2020: The Right to Sight’, in the following categories:
Long-term natural history of idiopathic epiretinal membranes with good visual acuity – (Eye Journal)
Long-term natural history of idiopathic epiretinal membranes with good visual acuity Long-term natural history of idiopathic epiretinal membranes with good visual acuity, Published online: 19 April 2019; doi:10.1038/s41433-019-0397-z Long-term natural history of idiopathic epiretinal membranes with good visual acuity
A hidden footprint: embryological origins of age related macular degeneration – (Eye Journal)
A hidden footprint: embryological origins of age related macular degeneration A hidden footprint: embryological origins of age related macular degeneration, Published online: 17 April 2019; doi:10.1038/s41433-019-0444-9 A hidden footprint: embryological origins of age related macular degeneration
Visual Function Questionnaire as an outcome measure for homonymous hemianopia: subscales and supplementary questions, analysis from the VISION trial – (Eye Journal)
Visual Function Questionnaire as an outcome measure for homonymous hemianopia: subscales and supplementary questions, analysis from the VISION trial Visual Function Questionnaire as an outcome measure for homonymous hemianopia: subscales and supplementary questions, analysis from the VISION trial, Published online: 17 April 2019; doi:10.1038/s41433-019-0441-z Visual Function Questionnaire as an outcome measure for homonymous hemianopia: subscales
Tyrosinase (TYR) gene sequencing and literature review reveals recurrent mutations and multiple population founder gene mutations as causative of oculocutaneous albinism (OCA) in Pakistani families – (Eye Journal)
Tyrosinase (TYR) gene sequencing and literature review reveals recurrent mutations and multiple population founder gene mutations as causative of oculocutaneous albinism (OCA) in Pakistani families <i>Tyrosinase (TYR)</i> gene sequencing and literature review reveals recurrent mutations and multiple population founder gene mutations as causative of oculocutaneous albinism (OCA) in Pakistani families, Published online: 17 April 2019;