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David Birch
David Birch
Chief Scientific and Executive Officer, Retina Foundation of the Southwest
Verified email at retinafoundation.org
Title
Cited by
Cited by
Year
Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice
J Weng, NL Mata, SM Azarian, RT Tzekov, DG Birch, GH Travis
Cell 98 (1), 13-23, 1999
9751999
A randomized controlled trial of early dietary supply of long-chain polyunsaturated fatty acids and mental development in term infants
EE Birch, S Garfield, DR Hoffman, R Uauy, DG Birch
Developmental medicine and child neurology 42 (3), 174-181, 2000
9392000
Effect of dietary omega-3 fatty acids on retinal function of very-low-birth-weight neonates
RD Uauy, DG Birch, EE Birch, JE Tyson, DR Hoffman
Pediatric research 28 (5), 485-492, 1990
7511990
Visual acuity and the essentiality of docosahexaenoic acid and arachidonic acid in the diet of term infants
EE Birch, DR Hoffman, R Uauy, DG Birch, C Prestidge
Pediatric research 44 (2), 201-209, 1998
6951998
Essential fatty acids in visual and brain development
R Uauy, DR Hoffman, P Peirano, DG Birch, EE Birch
Lipids 36 (9), 885-895, 2001
6212001
Dietary essential fatty acid supply and visual acuity development.
EE Birch, DG Birch, DR Hoffman, R Uauy
Investigative ophthalmology & visual science 33 (11), 3242-3253, 1992
5411992
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
NT Bech-Hansen, MJ Naylor, TA Maybaum, RL Sparkes, B Koop, ...
Nature genetics 26 (3), 319-323, 2000
4092000
Retinal development in very-low-birth-weight infants fed diets differing in omega-3 fatty acids.
DG Birch, EE Birch, DR Hoffman, RD Uauy
Investigative Ophthalmology & Visual Science 33 (8), 2365-2376, 1992
4001992
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies
MM Sohocki, SP Daiger, SJ Bowne, JA Rodriquez, H Northrup, ...
Human mutation 17 (1), 42-51, 2001
3912001
Five-year safety and performance results from the Argus II retinal prosthesis system clinical trial
L da Cruz, JD Dorn, MS Humayun, G Dagnelie, J Handa, PO Barale, ...
Ophthalmology 123 (10), 2248-2254, 2016
3752016
Natural course of retinitis pigmentosa over a three-year interval
EL Berson, MA Sandberg, B Rosner, DG Birch, AH Hanson
American journal of ophthalmology 99 (3), 240-251, 1985
3751985
Ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for treatment of geographic atrophy in age-related macular degeneration
K Zhang, JJ Hopkins, JS Heier, DG Birch, LS Halperin, TA Albini, ...
Proceedings of the National Academy of Sciences 108 (15), 6241-6245, 2011
3522011
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene
MM Sohocki, LS Sullivan, HA Mintz-Hittner, D Birch, JR Heckenlively, ...
The American Journal of Human Genetics 63 (5), 1307-1315, 1998
3361998
Standardized full-field electroretinography: normal values and their variation with age
DG Birch, JL Anderson
Archives of ophthalmology 110 (11), 1571-1576, 1992
3351992
Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families
LS Sullivan, SJ Bowne, DG Birch, D Hughbanks-Wheaton, ...
Investigative ophthalmology & visual science 47 (7), 3052-3064, 2006
3252006
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis
MM Sohocki, SJ Bowne, LS Sullivan, S Blackshaw, CL Cepko, AM Payne, ...
Nature genetics 24 (1), 79-83, 2000
3232000
Visual and brain function measurements in studies of n-3 fatty acid requirements of infants
R Uauy, E Birch, D Birch, P Peirano
The Journal of pediatrics 120 (4), S168-S180, 1992
3071992
Breast-feeding and optimal visual development
E Birch, D Birch, D Hoffman, L Hale, M Everett, R Uauy
Journal of Pediatric Ophthalmology & Strabismus 30 (1), 33-38, 1993
3041993
Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa
SJ Bowne, LS Sullivan, SH Blanton, CL Cepko, S Blackshaw, DG Birch, ...
Human molecular genetics 11 (5), 559-568, 2002
2902002
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice
Z Yang, Y Chen, C Lillo, J Chien, Z Yu, M Michaelides, M Klein, ...
The Journal of clinical investigation 118 (8), 2908-2916, 2008
2892008
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