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Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosaMargaret M DeAngelis, Jonna L Grimsby, Michael A Sandberg, et al.American Journal of Human Genetics|October 18, 2003
RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosaDror Sharon, Michael A Sandberg, Vivian W Rabe, et al.Journal of Neurochemistry|April 20, 2007
Neurochemical, morphological, and neurophysiological abnormalities in retinas of Sandhoff and GM1 gangliosidosis miceChristine A Denny, Joseph Alroy, Basil S Pawlyk, et al.Eneuro|February 21, 2019
Modes of Accessing Bicarbonate for the Regulation of Membrane Guanylate Cyclase (ROS-GC) in Retinal Rods and ConesClint L Makino, Teresa Duda, Alexandre Pertzev, et al.Investigative Ophthalmology & Visual Science|July 22, 2008
Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A geneMichael A Sandberg, Bernard Rosner, Carol Weigel-DiFranco, et al.Investigative Ophthalmology & Visual Science|April 27, 2005
Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226AsnYuko Wada, Michael A Sandberg, Terri L McGee, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|March 14, 2012
Genotype-phenotype correlations in Bardet-Biedl syndromeAnthony B Daniels, Michael A Sandberg, Jianjun Chen, et al.Proceedings of the National Academy of Sciences of the United States of America|December 14, 2004
Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone functionKoji M Nishiguchi, James S Friedman, Michael A Sandberg, et al.JAMA Ophthalmology|July 5, 2014
The relationship of central foveal thickness to urinary iodine concentration in retinitis pigmentosa with or without cystoid macular edemaMichael A Sandberg, Elizabeth N Pearce, Shyana Harper, et al.Ophthalmic Genetics|September 27, 2007
Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogramSureka Thiagalingam, Terri L McGee, Richard G Weleber, et al.Pageof 5