David Birch
David Birch
Chief Scientific and Executive Officer, Retina Foundation of the Southwest
Подтвержден адрес электронной почты в домене retinafoundation.org
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
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
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
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
Essential fatty acids in visual and brain development
R Uauy, DR Hoffman, P Peirano, DG Birch, EE Birch
Lipids 36 (9), 885-895, 2001
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
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
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
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
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
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
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
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
Standardized full-field electroretinography: normal values and their variation with age
DG Birch, JL Anderson
Archives of ophthalmology 110 (11), 1571-1576, 1992
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
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
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
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
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
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
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Статьи 1–20