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Eckart Apfelstedt-Sylla

Showing results (1-10 of 12) with videos related to

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Klinische Monatsblatter Fur Augenheilkunde|November 1, 2002
[Horner's syndrome in dissection of the carotid artery after chiropractic manipulation]Daphne Gamer, Andreas Schuster, Klaus Aicher, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 11, 2017
Electroretinogram and visual field changes in a case of birdshot chorioretinopathyHisham Elbaz, Volker Besgen, Klara Rechberger, et al.
Ocular Immunology and Inflammation|July 16, 2005
Autoimmune retinopathy with RPE hypersensitivity and 'negative ERG' in X-linked hyper-IgM syndromeAndreas Schuster, Eckart Apfelstedt-Sylla, Carsten M Pusch, et al.
Vision Research|June 5, 2002
Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein typeHana Langrová, Daphne Gamer, Christoph Friedburg, et al.
International Journal of Molecular Medicine|December 8, 2004
Multifocal oscillatory potentials in CSNB1 and CSNB2 type congenital stationary night blindnessAndreas Schuster, Carsten M Pusch, Daphine Gamer, et al.
Investigative Ophthalmology & Visual Science|March 30, 2002
Alterations of slow and fast rod ERG signals in patients with molecularly confirmed Stargardt disease type 1Hendrik P N Scholl, Dorothea Besch, Reinhard Vonthein, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 25, 2002
Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX geneFelix K Jacobi, Sten Andréasson, Hana Langrova, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|May 10, 2002
Visual field constriction and electrophysiological changes associated with vigabatrinDorothea Besch, Anne Kurtenbach, Eckart Apfelstedt-Sylla, et al.
American Journal of Ophthalmology|April 30, 2003
A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindnessFelix Karl Jacobi, Christian P Hamel, Bernard Arnaud, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 13, 2004
Molecular basis of an inherited form of incomplete achromatopsiaDimitri Tränkner, Herbert Jägle, Susanne Kohl, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Klinische Monatsblatter Fur Augenheilkunde|November 1, 2002
[Horner's syndrome in dissection of the carotid artery after chiropractic manipulation]Daphne Gamer, Andreas Schuster, Klaus Aicher, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 11, 2017
Electroretinogram and visual field changes in a case of birdshot chorioretinopathyHisham Elbaz, Volker Besgen, Klara Rechberger, et al.
Ocular Immunology and Inflammation|July 16, 2005
Autoimmune retinopathy with RPE hypersensitivity and 'negative ERG' in X-linked hyper-IgM syndromeAndreas Schuster, Eckart Apfelstedt-Sylla, Carsten M Pusch, et al.
Vision Research|June 5, 2002
Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein typeHana Langrová, Daphne Gamer, Christoph Friedburg, et al.
International Journal of Molecular Medicine|December 8, 2004
Multifocal oscillatory potentials in CSNB1 and CSNB2 type congenital stationary night blindnessAndreas Schuster, Carsten M Pusch, Daphine Gamer, et al.
Investigative Ophthalmology & Visual Science|March 30, 2002
Alterations of slow and fast rod ERG signals in patients with molecularly confirmed Stargardt disease type 1Hendrik P N Scholl, Dorothea Besch, Reinhard Vonthein, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 25, 2002
Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX geneFelix K Jacobi, Sten Andréasson, Hana Langrova, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|May 10, 2002
Visual field constriction and electrophysiological changes associated with vigabatrinDorothea Besch, Anne Kurtenbach, Eckart Apfelstedt-Sylla, et al.
American Journal of Ophthalmology|April 30, 2003
A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindnessFelix Karl Jacobi, Christian P Hamel, Bernard Arnaud, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 13, 2004
Molecular basis of an inherited form of incomplete achromatopsiaDimitri Tränkner, Herbert Jägle, Susanne Kohl, et al.
Pageof 2