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Johannes C Fleischhauer

Showing results (1-10 of 10) with videos related to

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Investigative Ophthalmology & Visual Science|March 28, 2006
Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypesJohn Neidhardt, Daniel Barthelmes, Firouzeh Farahmand, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 22, 2002
The Pulfrich phenomenon in a large population of young healthy subjectsJohannes C Fleischhauer, Martina M Oetliker, Hans Oetliker, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Impact of optic media opacities and image compression on quantitative analysis of optical coherence tomographyChristoph Tappeiner, Daniel Barthelmes, Mathias H Abegg, et al.
American Journal of Physiology. Cell Physiology|June 11, 2002
Human trabecular meshwork cell volume regulationClaire H Mitchell, Johannes C Fleischhauer, W Daniel Stamer, et al.
Investigative Ophthalmology & Visual Science|April 29, 2008
A new method to monitor visual field defects caused by photoreceptor degeneration by quantitative optical coherence tomographyM Dominik Fischer, Johannes C Fleischhauer, Mark C Gillies, et al.
Investigative Ophthalmology & Visual Science|March 1, 2006
Quantitative analysis of OCT characteristics in patients with achromatopsia and blue-cone monochromatismDaniel Barthelmes, Florian K Sutter, Malaika M Kurz-Levin, et al.
Investigative Ophthalmology & Visual Science|March 29, 2007
Is pseudophakia a risk factor for neovascular age-related macular degeneration?Florian K P Sutter, Moreno Menghini, Daniel Barthelmes, et al.
American Journal of Physiology. Cell Physiology|December 14, 2004
Differential P1-purinergic modulation of human Schlemm's canal inner-wall cellsMike O Karl, Johannes C Fleischhauer, W Daniel Stamer, et al.
Investigative Ophthalmology & Visual Science|July 7, 2009
Genotyping microarray for CSNB-associated genesChristina Zeitz, Stephan Labs, Birgit Lorenz, et al.
Journal of Medical Genetics|September 12, 2006
Development of a genotyping microarray for Usher syndromeFrans P M Cremers, William J Kimberling, Maigi Külm, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Investigative Ophthalmology & Visual Science|March 28, 2006
Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypesJohn Neidhardt, Daniel Barthelmes, Firouzeh Farahmand, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 22, 2002
The Pulfrich phenomenon in a large population of young healthy subjectsJohannes C Fleischhauer, Martina M Oetliker, Hans Oetliker, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Impact of optic media opacities and image compression on quantitative analysis of optical coherence tomographyChristoph Tappeiner, Daniel Barthelmes, Mathias H Abegg, et al.
American Journal of Physiology. Cell Physiology|June 11, 2002
Human trabecular meshwork cell volume regulationClaire H Mitchell, Johannes C Fleischhauer, W Daniel Stamer, et al.
Investigative Ophthalmology & Visual Science|April 29, 2008
A new method to monitor visual field defects caused by photoreceptor degeneration by quantitative optical coherence tomographyM Dominik Fischer, Johannes C Fleischhauer, Mark C Gillies, et al.
Investigative Ophthalmology & Visual Science|March 1, 2006
Quantitative analysis of OCT characteristics in patients with achromatopsia and blue-cone monochromatismDaniel Barthelmes, Florian K Sutter, Malaika M Kurz-Levin, et al.
Investigative Ophthalmology & Visual Science|March 29, 2007
Is pseudophakia a risk factor for neovascular age-related macular degeneration?Florian K P Sutter, Moreno Menghini, Daniel Barthelmes, et al.
American Journal of Physiology. Cell Physiology|December 14, 2004
Differential P1-purinergic modulation of human Schlemm's canal inner-wall cellsMike O Karl, Johannes C Fleischhauer, W Daniel Stamer, et al.
Investigative Ophthalmology & Visual Science|July 7, 2009
Genotyping microarray for CSNB-associated genesChristina Zeitz, Stephan Labs, Birgit Lorenz, et al.
Journal of Medical Genetics|September 12, 2006
Development of a genotyping microarray for Usher syndromeFrans P M Cremers, William J Kimberling, Maigi Külm, et al.
Pageof 1