David G. Birch, PhD

Affiliations: 
Retina Foundation of the Southwest, Dallas, TX, United States 
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"David Birch"
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Publications

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Birch DG, Bennett LD, Duncan JL, et al. (2016) Long-term follow-up of patients with retinitis pigmentosa (RP) receiving intraocular ciliary neurotrophic factor implants. American Journal of Ophthalmology
Carr BC, Emigh CE, Bennett LD, et al. (2016) TOWARDS A TREATMENT FOR DIABETIC RETINOPATHY: Intravitreal Toxicity and Preclinical Safety Evaluation of Inducible Nitric Oxide Synthase Inhibitors. Retina (Philadelphia, Pa.)
Ghodasra DH, Chen A, Arevalo JF, et al. (2016) Worldwide Argus II implantation: recommendations to optimize patient outcomes. Bmc Ophthalmology. 16: 52
Smith TB, Parker M, Steinkamp PN, et al. (2016) Structure-Function Modeling of Optical Coherence Tomography and Standard Automated Perimetry in the Retina of Patients with Autosomal Dominant Retinitis Pigmentosa. Plos One. 11: e0148022
Shankar SP, Hughbanks-Wheaton DK, Birch DG, et al. (2016) Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers. Investigative Ophthalmology & Visual Science. 57: 349-59
Bennett LD, Wang YZ, Klein M, et al. (2016) Structure/Psychophysical Relationships in X-Linked Retinoschisis. Investigative Ophthalmology & Visual Science. 57: 332-7
Strauss RW, Ho A, Muñoz B, et al. (2016) The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies: Design and Baseline Characteristics: ProgStar Report No. 1. Ophthalmology. 123: 817-28
Weisschuh N, Mayer AK, Strom TM, et al. (2016) Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing. Plos One. 11: e0145951
Daiger SP, Sullivan LS, Bowne SJ, et al. (2016) Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP). Advances in Experimental Medicine and Biology. 854: 193-200
Scholl HP, Moore AT, Koenekoop RK, et al. (2015) Safety and Proof-of-Concept Study of Oral QLT091001 in Retinitis Pigmentosa Due to Inherited Deficiencies of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT). Plos One. 10: e0143846
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