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Gesa-Astrid Hahn

Showing results (1-10 of 8) with videos related to

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Developments in Ophthalmology|July 25, 2003
Support for patients loosing sightSusanne Trauzettel-Klosinski, Gesa-Astrid Hahn
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 30, 2008
Parafoveal letter recognition at reduced contrast in normal aging and in patients with risk factors for AMDGesa Astrid Hahn, Andre Messias, Manfred Mackeben, et al.
American Journal of Ophthalmology|June 12, 2018
Longitudinal Changes of Fixation Location and Stability Within 12 Months in Stargardt Disease: ProgStar Report No. 12Etienne M Schönbach, Rupert W Strauss, Xiangrong Kong, et al.
Ophthalmology. Retina|May 4, 2019
Fixation Location and Stability Using the MP-1 Microperimeter in Stargardt Disease: ProgStar Report No. 3Etienne M Schönbach, Mohamed A Ibrahim, Rupert W Strauss, et al.
JAMA Ophthalmology|May 26, 2017
Macular Sensitivity Measured With Microperimetry in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 7Etienne M Schönbach, Yulia Wolfson, Rupert W Strauss, et al.
The Journal of Clinical Investigation|November 13, 2018
Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel-associated retinopathyMarkus Burkard, Susanne Kohl, Timm Krätzig, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 20, 2022
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2023
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Developments in Ophthalmology|July 25, 2003
Support for patients loosing sightSusanne Trauzettel-Klosinski, Gesa-Astrid Hahn
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 30, 2008
Parafoveal letter recognition at reduced contrast in normal aging and in patients with risk factors for AMDGesa Astrid Hahn, Andre Messias, Manfred Mackeben, et al.
American Journal of Ophthalmology|June 12, 2018
Longitudinal Changes of Fixation Location and Stability Within 12 Months in Stargardt Disease: ProgStar Report No. 12Etienne M Schönbach, Rupert W Strauss, Xiangrong Kong, et al.
Ophthalmology. Retina|May 4, 2019
Fixation Location and Stability Using the MP-1 Microperimeter in Stargardt Disease: ProgStar Report No. 3Etienne M Schönbach, Mohamed A Ibrahim, Rupert W Strauss, et al.
JAMA Ophthalmology|May 26, 2017
Macular Sensitivity Measured With Microperimetry in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 7Etienne M Schönbach, Yulia Wolfson, Rupert W Strauss, et al.
The Journal of Clinical Investigation|November 13, 2018
Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel-associated retinopathyMarkus Burkard, Susanne Kohl, Timm Krätzig, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 20, 2022
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2023
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophyJoohyun Park, Arianna Tucci, Valentina Cipriani, et al.
Pageof 1