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Alan C Bird

Showing results (71-80 of 123) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
Macular dystrophy associated with the A3243G mitochondrial DNA mutation. Distinct retinal and associated features, disease variability, and characterization of asymptomatic family membersMichel Michaelides, Sharon A Jenkins, Doris-Eva Bamiou, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|November 7, 2007
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and updateAnthony G Robson, Michel Michaelides, Zubin Saihan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
Correlation of functional impairment and morphological alterations in patients with group 2A idiopathic juxtafoveal retinal telangiectasiaSteffen Schmitz-Valckenberg, Kristie Fan, Alex Nugent, et al.
Investigative Ophthalmology & Visual Science|July 29, 2003
Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuityAnthony G Robson, Ahmed El-Amir, Claire Bailey, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafnessCaren Bellmann, Magella M Neveu, Hendrik P N Scholl, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 26, 2010
The symmetry of phenotype between eyes of patients with early and late bilateral age-related macular degeneration (AMD)Samantha S Mann, Yvonne Rutishauser-Arnold, Tunde Peto, et al.
Angiogenesis|March 21, 2007
Progenitor cells and retinal angiogenesisMartin Friedlander, Michael I Dorrell, Matthew R Ritter, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
Complement factor H variant Y402H is a major risk determinant for geographic atrophy and choroidal neovascularization in smokers and nonsmokersTiina Sepp, Jane C Khan, Deborah A Thurlby, et al.
Retina (Philadelphia, Pa.)|June 4, 2009
Structural and functional changes over time in MacTel patientsSteffen Schmitz-Valckenberg, E E Lin Ong, Gary S Rubin, et al.
Investigative Ophthalmology & Visual Science|September 26, 2003
Expression of PRPF31 mRNA in patients with autosomal dominant retinitis pigmentosa: a molecular clue for incomplete penetrance?Eranga N Vithana, Leen Abu-Safieh, Lucia Pelosini, et al.
Pageof 13

Showing results (71-80 of 123) with videos related to

Sort By:
Pageof 13
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
Macular dystrophy associated with the A3243G mitochondrial DNA mutation. Distinct retinal and associated features, disease variability, and characterization of asymptomatic family membersMichel Michaelides, Sharon A Jenkins, Doris-Eva Bamiou, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|November 7, 2007
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and updateAnthony G Robson, Michel Michaelides, Zubin Saihan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
Correlation of functional impairment and morphological alterations in patients with group 2A idiopathic juxtafoveal retinal telangiectasiaSteffen Schmitz-Valckenberg, Kristie Fan, Alex Nugent, et al.
Investigative Ophthalmology & Visual Science|July 29, 2003
Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuityAnthony G Robson, Ahmed El-Amir, Claire Bailey, et al.
Investigative Ophthalmology & Visual Science|June 30, 2004
Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafnessCaren Bellmann, Magella M Neveu, Hendrik P N Scholl, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 26, 2010
The symmetry of phenotype between eyes of patients with early and late bilateral age-related macular degeneration (AMD)Samantha S Mann, Yvonne Rutishauser-Arnold, Tunde Peto, et al.
Angiogenesis|March 21, 2007
Progenitor cells and retinal angiogenesisMartin Friedlander, Michael I Dorrell, Matthew R Ritter, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
Complement factor H variant Y402H is a major risk determinant for geographic atrophy and choroidal neovascularization in smokers and nonsmokersTiina Sepp, Jane C Khan, Deborah A Thurlby, et al.
Retina (Philadelphia, Pa.)|June 4, 2009
Structural and functional changes over time in MacTel patientsSteffen Schmitz-Valckenberg, E E Lin Ong, Gary S Rubin, et al.
Investigative Ophthalmology & Visual Science|September 26, 2003
Expression of PRPF31 mRNA in patients with autosomal dominant retinitis pigmentosa: a molecular clue for incomplete penetrance?Eranga N Vithana, Leen Abu-Safieh, Lucia Pelosini, et al.
Pageof 13