David G. Birch, PhD
Affiliations: | Retina Foundation of the Southwest, Dallas, TX, United States |
Google:
"David Birch"Mean distance: 22.23
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Birch DG, Cheetham JK, Daiger SP, et al. (2023) Overcoming the Challenges to Clinical Development of X-Linked Retinitis Pigmentosa Therapies: Proceedings of an Expert Panel. Translational Vision Science & Technology. 12: 5 |
| Duncan JL, Cheng P, Maguire MG, et al. (2023) Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment through Two Years. American Journal of Ophthalmology |
| Conley SM, McClard CK, Mwoyosvi ML, et al. (2022) Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2. Investigative Ophthalmology & Visual Science. 63: 19 |
| Solaki M, Baumann B, Reuter P, et al. (2022) Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia. Human Mutation |
| Birch DG, Samarakoon L, Melia M, et al. (2022) The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A Gene. Investigative Ophthalmology & Visual Science. 63: 17 |
| Schönbach EM, Janeschitz-Kriegl L, Strauss RW, et al. (2021) The Progression of Stargardt Disease using Volumetric Hill of Vision Analyses Over 24 Months: ProgStar Report No.15. American Journal of Ophthalmology |
| Radojevic B, Jones K, Klein M, et al. (2021) Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene . Ophthalmic Genetics. 42: 15-22 |
| Zhai Y, Xu M, Dimopoulos IS, et al. (2020) Quantification of RPE Changes in Choroideremia Using a Photoshop-Based Method. Translational Vision Science & Technology. 9: 21 |
| Thompson DA, Iannaccone A, Ali RR, et al. (2020) Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium. Translational Vision Science & Technology. 9: 2 |
| Bennett LD, Klein M, John FT, et al. (2020) Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1). Translational Vision Science & Technology. 9: 14 |