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Edwin M Stone

Showing results (71-80 of 384) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|July 11, 2012
Inhibition of neovascularization but not fibrosis with the fluocinolone acetonide implant in autosomal dominant neovascular inflammatory vitreoretinopathyPaul S Tlucek, James C Folk, Jason A Orien, et al.
JAMA Ophthalmology|May 30, 2015
Apparent Usher Syndrome Caused by the Combination of BBS1-Associated Retinitis Pigmentosa and SLC26A4-Associated DeafnessAdam P DeLuca, Matthew C Weed, Christine M Haas, et al.
Journal of Glaucoma|July 1, 2004
Attitudes to predictive DNA testing for myocilin glaucoma: experience with a large Australian familyDanielle L Healey, Jamie E Craig, Colleen H Wilkinson, et al.
Retina (Philadelphia, Pa.)|December 10, 2013
The value of retinal imaging with infrared scanning laser ophthalmoscopy in patients with stargardt diseaseRobert Chun, Gerald A Fishman, Frederick T Collison, et al.
Ophthalmic Genetics|September 27, 2007
Retinal dysfunction in carriers of bardet-biedl syndromeLinda S Kim, Gerald A Fishman, William H Seiple, et al.
Investigative Ophthalmology & Visual Science|June 27, 2007
Differential macular and peripheral expression of bestrophin in human eyes and its implication for best diseaseRobert F Mullins, Markus H Kuehn, Elizabeth A Faidley, et al.
Molecular Vision|September 16, 2009
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern IndiaPeriasamy Sundaresan, P Vijayalakshmi, Stewart Thompson, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 10, 2019
Disruption of RPGR protein interaction network is the common feature of RPGR missense variations that cause XLRPQihong Zhang, Joseph C Giacalone, Charles Searby, et al.
Retina (Philadelphia, Pa.)|April 21, 2004
Clinical phenotype as a prognostic factor in Stargardt diseaseKean T Oh, Richard G Weleber, Dawn M Oh, et al.
Experimental Eye Research|July 18, 2009
Localization of complement 1 inhibitor (C1INH/SERPING1) in human eyes with age-related macular degenerationRobert F Mullins, Elizabeth A Faidley, Heather T Daggett, et al.
Pageof 39

Showing results (71-80 of 384) with videos related to

Sort By:
Pageof 39
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 11, 2012
Inhibition of neovascularization but not fibrosis with the fluocinolone acetonide implant in autosomal dominant neovascular inflammatory vitreoretinopathyPaul S Tlucek, James C Folk, Jason A Orien, et al.
JAMA Ophthalmology|May 30, 2015
Apparent Usher Syndrome Caused by the Combination of BBS1-Associated Retinitis Pigmentosa and SLC26A4-Associated DeafnessAdam P DeLuca, Matthew C Weed, Christine M Haas, et al.
Journal of Glaucoma|July 1, 2004
Attitudes to predictive DNA testing for myocilin glaucoma: experience with a large Australian familyDanielle L Healey, Jamie E Craig, Colleen H Wilkinson, et al.
Retina (Philadelphia, Pa.)|December 10, 2013
The value of retinal imaging with infrared scanning laser ophthalmoscopy in patients with stargardt diseaseRobert Chun, Gerald A Fishman, Frederick T Collison, et al.
Ophthalmic Genetics|September 27, 2007
Retinal dysfunction in carriers of bardet-biedl syndromeLinda S Kim, Gerald A Fishman, William H Seiple, et al.
Investigative Ophthalmology & Visual Science|June 27, 2007
Differential macular and peripheral expression of bestrophin in human eyes and its implication for best diseaseRobert F Mullins, Markus H Kuehn, Elizabeth A Faidley, et al.
Molecular Vision|September 16, 2009
Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern IndiaPeriasamy Sundaresan, P Vijayalakshmi, Stewart Thompson, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 10, 2019
Disruption of RPGR protein interaction network is the common feature of RPGR missense variations that cause XLRPQihong Zhang, Joseph C Giacalone, Charles Searby, et al.
Retina (Philadelphia, Pa.)|April 21, 2004
Clinical phenotype as a prognostic factor in Stargardt diseaseKean T Oh, Richard G Weleber, Dawn M Oh, et al.
Experimental Eye Research|July 18, 2009
Localization of complement 1 inhibitor (C1INH/SERPING1) in human eyes with age-related macular degenerationRobert F Mullins, Elizabeth A Faidley, Heather T Daggett, et al.
Pageof 39