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Edwin M Stone

Showing results (41-50 of 384) with videos related to

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Human Molecular Genetics|January 10, 2012
BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypesQihong Zhang, Seongjin Seo, Kevin Bugge, et al.
Ophthalmic Genetics|February 25, 2025
Retinal thickness and visual acuity in early-onset Stargardt disease follow a non-linear progression curve: implications for clinical trialsS Scott Whitmore, Douglas B Critser, Edwin M Stone, et al.
JAMA Ophthalmology|March 13, 2015
Autosomal Dominant Microcephaly Associated With Congenital Lymphedema and Chorioretinopathy Due to a Novel Mutation in KIF11Katrina Mears, Benjamin Bakall, Lisa A Harney, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|June 19, 2016
Distinguishing optic pathway glioma and retinitis pigmentosa with visual field testingMatthew C Weed, David R P Almeida, Eric K Chin, et al.
Investigative Ophthalmology & Visual Science|June 3, 2008
Divergent phenotypes of vision and accessory visual function in mice with visual cycle dysfunction (Rpe65 rd12) or retinal degeneration (rd/rd)Stewart Thompson, Robert F Mullins, Alisdair R Philp, et al.
Retina (Philadelphia, Pa.)|February 18, 2025
SPLIT OUTER PLEXIFORM LAYER APPEARANCE REPRESENTS AN ACQUIRED CONE DYSFUNCTION PHENOTYPE OF AUTOIMMUNE RETINOPATHYTimothy M Boyce, Christopher Fortenbach, Matthew Thurtell, et al.
Survey of Ophthalmology|December 31, 2002
Myocilin glaucomaJohn H Fingert, Edwin M Stone, Val C Sheffield, et al.
The European Journal of Neuroscience|April 17, 2008
Classical and melanopsin photoreception in irradiance detection: negative masking of locomotor activity by lightStewart Thompson, Russell G Foster, Edwin M Stone, et al.
Retinal Cases & Brief Reports|November 13, 2014
De novo mutation in a choroideremia carrierSimge Bozbeyoglu, Gerald A Fishman, Edwin M Stone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2005
Late development of vitelliform lesions and flecks in a patient with best disease: clinicopathologic correlationRobert F Mullins, Kean T Oh, Edward Heffron, et al.
Pageof 39

Showing results (41-50 of 384) with videos related to

Sort By:
Pageof 39
Human Molecular Genetics|January 10, 2012
BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypesQihong Zhang, Seongjin Seo, Kevin Bugge, et al.
Ophthalmic Genetics|February 25, 2025
Retinal thickness and visual acuity in early-onset Stargardt disease follow a non-linear progression curve: implications for clinical trialsS Scott Whitmore, Douglas B Critser, Edwin M Stone, et al.
JAMA Ophthalmology|March 13, 2015
Autosomal Dominant Microcephaly Associated With Congenital Lymphedema and Chorioretinopathy Due to a Novel Mutation in KIF11Katrina Mears, Benjamin Bakall, Lisa A Harney, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|June 19, 2016
Distinguishing optic pathway glioma and retinitis pigmentosa with visual field testingMatthew C Weed, David R P Almeida, Eric K Chin, et al.
Investigative Ophthalmology & Visual Science|June 3, 2008
Divergent phenotypes of vision and accessory visual function in mice with visual cycle dysfunction (Rpe65 rd12) or retinal degeneration (rd/rd)Stewart Thompson, Robert F Mullins, Alisdair R Philp, et al.
Retina (Philadelphia, Pa.)|February 18, 2025
SPLIT OUTER PLEXIFORM LAYER APPEARANCE REPRESENTS AN ACQUIRED CONE DYSFUNCTION PHENOTYPE OF AUTOIMMUNE RETINOPATHYTimothy M Boyce, Christopher Fortenbach, Matthew Thurtell, et al.
Survey of Ophthalmology|December 31, 2002
Myocilin glaucomaJohn H Fingert, Edwin M Stone, Val C Sheffield, et al.
The European Journal of Neuroscience|April 17, 2008
Classical and melanopsin photoreception in irradiance detection: negative masking of locomotor activity by lightStewart Thompson, Russell G Foster, Edwin M Stone, et al.
Retinal Cases & Brief Reports|November 13, 2014
De novo mutation in a choroideremia carrierSimge Bozbeyoglu, Gerald A Fishman, Edwin M Stone, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 16, 2005
Late development of vitelliform lesions and flecks in a patient with best disease: clinicopathologic correlationRobert F Mullins, Kean T Oh, Edward Heffron, et al.
Pageof 39