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Investigative Ophthalmology & Visual Science
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March 28, 2006
Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes
John Neidhardt, Daniel Barthelmes, Firouzeh Farahmand, et al.
Klinische Monatsblatter Fur Augenheilkunde
|
May 22, 2002
The Pulfrich phenomenon in a large population of young healthy subjects
Johannes 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 tomography
Christoph Tappeiner, Daniel Barthelmes, Mathias H Abegg, et al.
American Journal of Physiology. Cell Physiology
|
June 11, 2002
Human trabecular meshwork cell volume regulation
Claire 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 tomography
M 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 monochromatism
Daniel 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 cells
Mike O Karl, Johannes C Fleischhauer, W Daniel Stamer, et al.
Investigative Ophthalmology & Visual Science
|
July 7, 2009
Genotyping microarray for CSNB-associated genes
Christina Zeitz, Stephan Labs, Birgit Lorenz, et al.
Journal of Medical Genetics
|
September 12, 2006
Development of a genotyping microarray for Usher syndrome
Frans P M Cremers, William J Kimberling, Maigi Külm, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Investigative Ophthalmology & Visual Science
|
March 28, 2006
Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes
John Neidhardt, Daniel Barthelmes, Firouzeh Farahmand, et al.
Klinische Monatsblatter Fur Augenheilkunde
|
May 22, 2002
The Pulfrich phenomenon in a large population of young healthy subjects
Johannes 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 tomography
Christoph Tappeiner, Daniel Barthelmes, Mathias H Abegg, et al.
American Journal of Physiology. Cell Physiology
|
June 11, 2002
Human trabecular meshwork cell volume regulation
Claire 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 tomography
M 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 monochromatism
Daniel 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 cells
Mike O Karl, Johannes C Fleischhauer, W Daniel Stamer, et al.
Investigative Ophthalmology & Visual Science
|
July 7, 2009
Genotyping microarray for CSNB-associated genes
Christina Zeitz, Stephan Labs, Birgit Lorenz, et al.
Journal of Medical Genetics
|
September 12, 2006
Development of a genotyping microarray for Usher syndrome
Frans P M Cremers, William J Kimberling, Maigi Külm, et al.
Page
of 1