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Edwin M Stone

Showing results (81-90 of 384) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|June 11, 2003
ABCA4 gene sequence variations in patients with autosomal recessive cone-rod dystrophyGerald A Fishman, Edwin M Stone, David A Eliason, et al.
Ophthalmology|September 14, 2014
Vitritis in pediatric genetic retinal disordersMaria Stunkel, Sajag Bhattarai, Andrew Kemerley, et al.
Investigative Ophthalmology & Visual Science|July 29, 2003
De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosaSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophySamuel G Jacobson, Artur V Cideciyan, Jean Bennett, et al.
Annual Review of Vision Science|September 15, 2022
The Essential Role of the Choriocapillaris in Vision: Novel Insights from Imaging and Molecular BiologyKelly Mulfaul, Jonathan F Russell, Andrew P Voigt, et al.
Experimental Eye Research|July 7, 2011
Elevated membrane attack complex in human choroid with high risk complement factor H genotypesRobert F Mullins, Aaron D Dewald, Luan M Streb, et al.
Retina (Philadelphia, Pa.)|December 8, 2004
Electroretinographic findings in patients with Stargardt disease and fundus flavimaculatusKean T Oh, Richard G Weleber, Edwin M Stone, et al.
Investigative Ophthalmology & Visual Science|February 13, 2014
Structural and biochemical analyses of choroidal thickness in human donor eyesElliott H Sohn, Aditi Khanna, Budd A Tucker, et al.
Human Molecular Genetics|January 10, 2006
Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia functionHsan-Jan Yen, Marwan K Tayeh, Robert F Mullins, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Ocular phenotypes of three genetic variants of Bardet-Biedl syndromeElise Héon, Carol Westall, Rivka Carmi, et al.
Pageof 39

Showing results (81-90 of 384) with videos related to

Sort By:
Pageof 39
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 11, 2003
ABCA4 gene sequence variations in patients with autosomal recessive cone-rod dystrophyGerald A Fishman, Edwin M Stone, David A Eliason, et al.
Ophthalmology|September 14, 2014
Vitritis in pediatric genetic retinal disordersMaria Stunkel, Sajag Bhattarai, Andrew Kemerley, et al.
Investigative Ophthalmology & Visual Science|July 29, 2003
De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosaSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophySamuel G Jacobson, Artur V Cideciyan, Jean Bennett, et al.
Annual Review of Vision Science|September 15, 2022
The Essential Role of the Choriocapillaris in Vision: Novel Insights from Imaging and Molecular BiologyKelly Mulfaul, Jonathan F Russell, Andrew P Voigt, et al.
Experimental Eye Research|July 7, 2011
Elevated membrane attack complex in human choroid with high risk complement factor H genotypesRobert F Mullins, Aaron D Dewald, Luan M Streb, et al.
Retina (Philadelphia, Pa.)|December 8, 2004
Electroretinographic findings in patients with Stargardt disease and fundus flavimaculatusKean T Oh, Richard G Weleber, Edwin M Stone, et al.
Investigative Ophthalmology & Visual Science|February 13, 2014
Structural and biochemical analyses of choroidal thickness in human donor eyesElliott H Sohn, Aditi Khanna, Budd A Tucker, et al.
Human Molecular Genetics|January 10, 2006
Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia functionHsan-Jan Yen, Marwan K Tayeh, Robert F Mullins, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Ocular phenotypes of three genetic variants of Bardet-Biedl syndromeElise Héon, Carol Westall, Rivka Carmi, et al.
Pageof 39