Eliot Berson, MD

Massachusetts Eye & Ear  Harvard University, Cambridge, MA, United States 
"Eliot Berson"
Mean distance: 20.26
BETA: Related 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.

Berson EL, Weigel-DiFranco C, Rosner B, et al. (2018) Association of Vitamin A Supplementation With Disease Course in Children With Retinitis Pigmentosa. Jama Ophthalmology
Pawlyk BS, Bulgakov OV, Sun X, et al. (2015) Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of x-linked retinitis pigmentosa. Gene Therapy
Comander J, Weigel-DiFranco C, Sandberg MA, et al. (2015) Visual Function in Carriers of X-Linked Retinitis Pigmentosa. Ophthalmology. 122: 1899-906
Venturini G, Koskiniemi-Kuendig H, Harper S, et al. (2015) Two specific mutations are prevalent causes of recessive retinitis pigmentosa in North American patients of Jewish ancestry. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 285-90
Comander J, Weigel-DiFranco C, Sandberg MA, et al. (2015) Visual Function in Carriers of X-Linked Retinitis Pigmentosa Ophthalmology
Bujakowska KM, Consugar M, Place E, et al. (2014) Targeted exon sequencing in Usher syndrome type I. Investigative Ophthalmology & Visual Science. 55: 8488-96
Sandberg MA, Pearce EN, Harper S, et al. (2014) The relationship of central foveal thickness to urinary iodine concentration in retinitis pigmentosa with or without cystoid macular edema. Jama Ophthalmology. 132: 1209-14
Benaglio P, San Jose PF, Avila-Fernandez A, et al. (2014) Mutational screening of splicing factor genes in cases with autosomal dominant retinitis pigmentosa. Molecular Vision. 20: 843-51
Venturini G, Di Gioia SA, Harper S, et al. (2014) Molecular genetics of FAM161A in North American patients with early-onset retinitis pigmentosa. Plos One. 9: e92479
Mackay DS, Borman AD, Sui R, et al. (2014) Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype-Phenotype Correlations. [34, 11, 1537-1546, 10.1002/humu.22398] Human Mutation. 35: 150-150
See more...