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M A Sandberg

Showing results (51-60 of 72) with videos related to

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American Journal of Ophthalmology|May 15, 1991
Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucineE L Berson, B Rosner, M A Sandberg, et al.
American Journal of Ophthalmology|November 15, 1991
Hydroxychloroquine retinopathyA Weiner, M A Sandberg, A R Gaudio, et al.
Vision Research|January 1, 1987
Effects of IBMX on the ERG of the isolated perfused cat eyeM A Sandberg, B S Pawlyk, W G Crane, et al.
Investigative Ophthalmology & Visual Science|October 1, 1995
Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutationP J Rosenfeld, L B Hahn, M A Sandberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 22, 2000
A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3)D H Hong, B S Pawlyk, J Shang, et al.
Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association for Ocular Pharmacology and Therapeutics|September 8, 2000
Endothelin-1-mediated retinal artery vasospasm and the rabbit electroretinogramT A Ciulla, B S Pawlyk, A Harris, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 31, 1998
Rod and cone function in the Nougaret form of stationary night blindnessM A Sandberg, B S Pawlyk, J Dan, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual functionD Sharon, G A Bruns, T L McGee, et al.
Experimental Eye Research|September 1, 1997
13-cis-retinoic acid in silicone-fluorosilicone copolymer oil in a rabbit model of proliferative vitreoretinopathyA A Veloso, E F Kadrmas, J M Larrosa, et al.
Nature Genetics|June 1, 1992
A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosaP J Rosenfeld, G S Cowley, T L McGee, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
American Journal of Ophthalmology|May 15, 1991
Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucineE L Berson, B Rosner, M A Sandberg, et al.
American Journal of Ophthalmology|November 15, 1991
Hydroxychloroquine retinopathyA Weiner, M A Sandberg, A R Gaudio, et al.
Vision Research|January 1, 1987
Effects of IBMX on the ERG of the isolated perfused cat eyeM A Sandberg, B S Pawlyk, W G Crane, et al.
Investigative Ophthalmology & Visual Science|October 1, 1995
Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutationP J Rosenfeld, L B Hahn, M A Sandberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 22, 2000
A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3)D H Hong, B S Pawlyk, J Shang, et al.
Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association for Ocular Pharmacology and Therapeutics|September 8, 2000
Endothelin-1-mediated retinal artery vasospasm and the rabbit electroretinogramT A Ciulla, B S Pawlyk, A Harris, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 31, 1998
Rod and cone function in the Nougaret form of stationary night blindnessM A Sandberg, B S Pawlyk, J Dan, et al.
Investigative Ophthalmology & Visual Science|August 11, 2000
X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual functionD Sharon, G A Bruns, T L McGee, et al.
Experimental Eye Research|September 1, 1997
13-cis-retinoic acid in silicone-fluorosilicone copolymer oil in a rabbit model of proliferative vitreoretinopathyA A Veloso, E F Kadrmas, J M Larrosa, et al.
Nature Genetics|June 1, 1992
A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosaP J Rosenfeld, G S Cowley, T L McGee, et al.
Pageof 8