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Investigative Ophthalmology & Visual Science|August 1, 1995
Clinical expression correlates with location of rhodopsin mutation in dominant retinitis pigmentosaM A Sandberg, C Weigel-DiFranco, T P Dryja, et al.
Nature Genetics|July 1, 1993
Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindnessT P Dryja, E L Berson, V R Rao, et al.
Experimental Eye Research|June 1, 1988
Diurnal rhythm in the electroretinogram of the Royal College of Surgeons (RCS) pigmented ratM A Sandberg, B S Pawlyk, W G Crane, et al.
Investigative Ophthalmology & Visual Science|September 1, 2000
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosaT P Dryja, J A McEvoy, T L McGee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 26, 2014
Two specific mutations are prevalent causes of recessive retinitis pigmentosa in North American patients of Jewish ancestryGiulia Venturini, Hanna Koskiniemi-Kuendig, Shyana Harper, et al.
Investigative Ophthalmology & Visual Science|August 27, 2005
The association between visual acuity and central retinal thickness in retinitis pigmentosaMichael A Sandberg, Robert J Brockhurst, Alexander R Gaudio, et al.
Investigative Ophthalmology & Visual Science|June 17, 2008
Visual acuity is related to parafoveal retinal thickness in patients with retinitis pigmentosa and macular cystsMichael A Sandberg, Robert J Brockhurst, Alexander R Gaudio, et al.
American Journal of Ophthalmology|October 9, 2001
Melanoma-associated retinopathy and recurrent exudative retinal detachments in a patient with choroidal melanomaD N Zacks, M K Pinnolis, E L Berson, et al.
Investigative Ophthalmology & Visual Science|March 21, 1998
Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindnessK C Sippel, J D DeStefano, E L Berson, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 1995
Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosaM E McLaughlin, T L Ehrhart, E L Berson, et al.
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