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Edwin M Stone

Showing results (181-190 of 384) with videos related to

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Journal of Glaucoma|June 5, 2003
Tonography demonstrates reduced facility of outflow of aqueous humor in myocilin mutation carriersColleen H Wilkinson, David van der Straaten, Jamie E Craig, et al.
Journal of Glaucoma|February 1, 2002
Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from BrazilAdriana Silva Borges, Remo Susanna, José Carlos Eudes Carani, et al.
Experimental Eye Research|March 12, 2014
Mechanical properties of murine and porcine ocular tissues in compressionKristan S Worthington, Luke A Wiley, Alexandra M Bartlett, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 16, 2012
Intravitreal bevacizumab for peripapillary choroidal neovascular membranesAndrew S Davis, James C Folk, Stephen R Russell, et al.
Human Mutation|June 1, 2010
Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRLLorenzo L Nichols, Ramakrishna P Alur, Elangovan Boobalan, et al.
Ophthalmology. Glaucoma|May 24, 2023
Mutations in EFEMP1 in Patients with Juvenile Open-Angle GlaucomaAminatta Z Tejan-Kamara, Erin A Boese, Andrew E Pouw, et al.
JAMA Ophthalmology|February 13, 2015
Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal DystrophiesSuma P Shankar, David G Birch, Richard S Ruiz, et al.
Molecular Vision|June 9, 2009
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganizationSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Human Mutation|January 6, 2006
Prioritizing regions of candidate genes for efficient mutation screeningTerry A Braun, Suma P Shankar, Steve Davis, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 14, 2007
No association between variations in the WDR36 gene and primary open-angle glaucomaJohn H Fingert, Wallace L M Alward, Young H Kwon, et al.
Pageof 39

Showing results (181-190 of 384) with videos related to

Sort By:
Pageof 39
Journal of Glaucoma|June 5, 2003
Tonography demonstrates reduced facility of outflow of aqueous humor in myocilin mutation carriersColleen H Wilkinson, David van der Straaten, Jamie E Craig, et al.
Journal of Glaucoma|February 1, 2002
Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from BrazilAdriana Silva Borges, Remo Susanna, José Carlos Eudes Carani, et al.
Experimental Eye Research|March 12, 2014
Mechanical properties of murine and porcine ocular tissues in compressionKristan S Worthington, Luke A Wiley, Alexandra M Bartlett, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 16, 2012
Intravitreal bevacizumab for peripapillary choroidal neovascular membranesAndrew S Davis, James C Folk, Stephen R Russell, et al.
Human Mutation|June 1, 2010
Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRLLorenzo L Nichols, Ramakrishna P Alur, Elangovan Boobalan, et al.
Ophthalmology. Glaucoma|May 24, 2023
Mutations in EFEMP1 in Patients with Juvenile Open-Angle GlaucomaAminatta Z Tejan-Kamara, Erin A Boese, Andrew E Pouw, et al.
JAMA Ophthalmology|February 13, 2015
Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal DystrophiesSuma P Shankar, David G Birch, Richard S Ruiz, et al.
Molecular Vision|June 9, 2009
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganizationSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Human Mutation|January 6, 2006
Prioritizing regions of candidate genes for efficient mutation screeningTerry A Braun, Suma P Shankar, Steve Davis, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 14, 2007
No association between variations in the WDR36 gene and primary open-angle glaucomaJohn H Fingert, Wallace L M Alward, Young H Kwon, et al.
Pageof 39