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F Fitzke

Showing results (11-20 of 21) with videos related to

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Eye (London, England)|October 26, 2005
Pars plana vitrectomy for diabetic macular oedema: OCT and functional correlationsJ I Patel, P G Hykin, M Schadt, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|November 18, 2003
Macular pigment: quantitative analysis on autofluorescence imagesM Trieschmann, G Spital, A Lommatzsch, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|December 1, 1992
[Corneal opacity after photorefractive keratectomy with an excimer laser. Cause, objective measurement and functional consequences]C P Lohmann, D S Gartry, M K Muir, et al.
Eye (London, England)|July 30, 2005
Diabetic macular oedema: pilot randomised trial of pars plana vitrectomy vs macular argon photocoagulationJ I Patel, P G Hykin, M Schadt, et al.
Eye (London, England)|June 30, 2012
Heritability of the spatial distribution and peak density of macular pigment: a classical twin studyR E Hogg, E L Ong, M Chamberlain, et al.
Human Molecular Genetics|April 1, 1992
A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosaC F Inglehearn, T J Keen, R Bashir, et al.
Nature Genetics|March 1, 1993
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophyJ Wells, J Wroblewski, J Keen, et al.
The British Journal of Ophthalmology|August 1, 1993
Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic studyA T Moore, F Fitzke, M Jay, et al.
Ophthalmology|January 1, 1994
Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow geneJ J Wroblewski, J A Wells, A Eckstein, et al.
Archives of Biochemistry and Biophysics|November 7, 2006
Xanthophyll accumulation in the human retina during supplementation with lutein or zeaxanthin - the LUXEA (LUtein Xanthophyll Eye Accumulation) studyWolfgang Schalch, William Cohn, Felix M Barker, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Eye (London, England)|October 26, 2005
Pars plana vitrectomy for diabetic macular oedema: OCT and functional correlationsJ I Patel, P G Hykin, M Schadt, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|November 18, 2003
Macular pigment: quantitative analysis on autofluorescence imagesM Trieschmann, G Spital, A Lommatzsch, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|December 1, 1992
[Corneal opacity after photorefractive keratectomy with an excimer laser. Cause, objective measurement and functional consequences]C P Lohmann, D S Gartry, M K Muir, et al.
Eye (London, England)|July 30, 2005
Diabetic macular oedema: pilot randomised trial of pars plana vitrectomy vs macular argon photocoagulationJ I Patel, P G Hykin, M Schadt, et al.
Eye (London, England)|June 30, 2012
Heritability of the spatial distribution and peak density of macular pigment: a classical twin studyR E Hogg, E L Ong, M Chamberlain, et al.
Human Molecular Genetics|April 1, 1992
A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosaC F Inglehearn, T J Keen, R Bashir, et al.
Nature Genetics|March 1, 1993
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophyJ Wells, J Wroblewski, J Keen, et al.
The British Journal of Ophthalmology|August 1, 1993
Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic studyA T Moore, F Fitzke, M Jay, et al.
Ophthalmology|January 1, 1994
Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow geneJ J Wroblewski, J A Wells, A Eckstein, et al.
Archives of Biochemistry and Biophysics|November 7, 2006
Xanthophyll accumulation in the human retina during supplementation with lutein or zeaxanthin - the LUXEA (LUtein Xanthophyll Eye Accumulation) studyWolfgang Schalch, William Cohn, Felix M Barker, et al.
Pageof 3