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Acta Anatomica
|
December 1, 1998
Inner retinal function in hereditary retinal dystrophies
K Ruether, U Kellner
German Journal of Ophthalmology
|
November 1, 1993
Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type
K Ruether, E Apfelstedt-Sylla, E Zrenner
German Journal of Ophthalmology
|
November 1, 1996
Electroretinographic campimetry in a patient with crystalline retinopathy
U Kretschmann, T Usui, K Ruether, et al.
Vision Research
|
January 20, 1999
Spatial cone activity distribution in diseases of the posterior pole determined by multifocal electroretinography
U Kretschmann, M Seeliger, K Ruether, et al.
Investigative Ophthalmology & Visual Science
|
October 29, 2000
Abnormalities of the photoreceptor-bipolar cell synapse in a substrain of C57BL/10 mice
K Ruether, J Grosse, E Matthiessen, et al.
Eye (London, England)
|
September 16, 2008
Lipofuscin- and melanin-related fundus autofluorescence visualize different retinal pigment epithelial alterations in patients with retinitis pigmentosa
U Kellner, S Kellner, B H F Weber, et al.
The British Journal of Ophthalmology
|
May 29, 1998
Multifocal electroretinography in patients with Stargardt's macular dystrophy
U Kretschmann, M W Seeliger, K Ruether, et al.
Investigative Ophthalmology & Visual Science
|
March 1, 1997
Retinoschisislike alterations in the mouse eye caused by gene targeting of the Norrie disease gene
K Ruether, D van de Pol, G Jaissle, et al.
Neuron
|
February 22, 2001
Disruption of ClC-3, a chloride channel expressed on synaptic vesicles, leads to a loss of the hippocampus
S M Stobrawa, T Breiderhoff, S Takamori, et al.
Molecular and Cellular Biology
|
May 29, 2000
Disruption of the 11-cis-retinol dehydrogenase gene leads to accumulation of cis-retinols and cis-retinyl esters
C A Driessen, H J Winkens, K Hoffmann, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Acta Anatomica
|
December 1, 1998
Inner retinal function in hereditary retinal dystrophies
K Ruether, U Kellner
German Journal of Ophthalmology
|
November 1, 1993
Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type
K Ruether, E Apfelstedt-Sylla, E Zrenner
German Journal of Ophthalmology
|
November 1, 1996
Electroretinographic campimetry in a patient with crystalline retinopathy
U Kretschmann, T Usui, K Ruether, et al.
Vision Research
|
January 20, 1999
Spatial cone activity distribution in diseases of the posterior pole determined by multifocal electroretinography
U Kretschmann, M Seeliger, K Ruether, et al.
Investigative Ophthalmology & Visual Science
|
October 29, 2000
Abnormalities of the photoreceptor-bipolar cell synapse in a substrain of C57BL/10 mice
K Ruether, J Grosse, E Matthiessen, et al.
Eye (London, England)
|
September 16, 2008
Lipofuscin- and melanin-related fundus autofluorescence visualize different retinal pigment epithelial alterations in patients with retinitis pigmentosa
U Kellner, S Kellner, B H F Weber, et al.
The British Journal of Ophthalmology
|
May 29, 1998
Multifocal electroretinography in patients with Stargardt's macular dystrophy
U Kretschmann, M W Seeliger, K Ruether, et al.
Investigative Ophthalmology & Visual Science
|
March 1, 1997
Retinoschisislike alterations in the mouse eye caused by gene targeting of the Norrie disease gene
K Ruether, D van de Pol, G Jaissle, et al.
Neuron
|
February 22, 2001
Disruption of ClC-3, a chloride channel expressed on synaptic vesicles, leads to a loss of the hippocampus
S M Stobrawa, T Breiderhoff, S Takamori, et al.
Molecular and Cellular Biology
|
May 29, 2000
Disruption of the 11-cis-retinol dehydrogenase gene leads to accumulation of cis-retinols and cis-retinyl esters
C A Driessen, H J Winkens, K Hoffmann, et al.
Page
of 1