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Sten Andreasson

Showing results (11-20 of 28) with videos related to

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Investigative Ophthalmology & Visual Science|June 12, 2009
The porcine retinal vasculature accessed using an endovascular approach: a new experimental model for retinal ischemiaHåkan Morén, Per Undrén, Bodil Gesslein, et al.
Investigative Ophthalmology & Visual Science|April 9, 2010
Evaluation of macular structure and function by OCT and electrophysiology in patients with vitelliform macular dystrophy due to mutations in BEST1Patrik Schatz, Hanna Bitner, Birgit Sander, et al.
Clinical Ophthalmology (Auckland, N.Z.)|July 10, 2013
Macular dysfunction in drusen maculopathy assessed with multifocal electroretinogram and optical coherence tomographyJose G Garcia-Garcia, Jose M Ruiz-Moreno, Kristina Holm, et al.
Translational Vision Science & Technology|September 25, 2020
Longitudinal Changes of Macular Curvature in Patients with Retinitis PigmentosaMonika Meinert, Shinji Ueno, Shiori Komori, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 28, 2016
Most patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency develop pathological or subnormal retinal functionKristina Teär Fahnehjelm, Ying Liu, David Olsson, et al.
American Journal of Ophthalmology|November 29, 2008
Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutationsAgnes B Renner, Britta S Fiebig, Bernhard H F Weber, et al.
Molecular Vision|January 29, 2003
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL geneCeren Acar, Alan J Mears, Beverly M Yashar, et al.
Human Molecular Genetics|December 4, 2010
Decreased catalytic activity and altered activation properties of PDE6C mutants associated with autosomal recessive achromatopsiaTanja Grau, Nikolai O Artemyev, Thomas Rosenberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 6, 2009
A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C geneBo Chang, Tanja Grau, Susann Dangel, et al.
Investigative Ophthalmology & Visual Science|May 31, 2002
A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophyDawn L Thiselton, Christiane Alexander, Jan-Willem Taanman, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Investigative Ophthalmology & Visual Science|June 12, 2009
The porcine retinal vasculature accessed using an endovascular approach: a new experimental model for retinal ischemiaHåkan Morén, Per Undrén, Bodil Gesslein, et al.
Investigative Ophthalmology & Visual Science|April 9, 2010
Evaluation of macular structure and function by OCT and electrophysiology in patients with vitelliform macular dystrophy due to mutations in BEST1Patrik Schatz, Hanna Bitner, Birgit Sander, et al.
Clinical Ophthalmology (Auckland, N.Z.)|July 10, 2013
Macular dysfunction in drusen maculopathy assessed with multifocal electroretinogram and optical coherence tomographyJose G Garcia-Garcia, Jose M Ruiz-Moreno, Kristina Holm, et al.
Translational Vision Science & Technology|September 25, 2020
Longitudinal Changes of Macular Curvature in Patients with Retinitis PigmentosaMonika Meinert, Shinji Ueno, Shiori Komori, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 28, 2016
Most patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency develop pathological or subnormal retinal functionKristina Teär Fahnehjelm, Ying Liu, David Olsson, et al.
American Journal of Ophthalmology|November 29, 2008
Phenotypic variability and long-term follow-up of patients with known and novel PRPH2/RDS gene mutationsAgnes B Renner, Britta S Fiebig, Bernhard H F Weber, et al.
Molecular Vision|January 29, 2003
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL geneCeren Acar, Alan J Mears, Beverly M Yashar, et al.
Human Molecular Genetics|December 4, 2010
Decreased catalytic activity and altered activation properties of PDE6C mutants associated with autosomal recessive achromatopsiaTanja Grau, Nikolai O Artemyev, Thomas Rosenberg, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 6, 2009
A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C geneBo Chang, Tanja Grau, Susann Dangel, et al.
Investigative Ophthalmology & Visual Science|May 31, 2002
A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophyDawn L Thiselton, Christiane Alexander, Jan-Willem Taanman, et al.
Pageof 3