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Clinical Protocols for the Evaluation of Rod Function.

Autor: Stingl, Krunoslav^1,2 (AUTHOR), Stingl, Katarina^1,2 (AUTHOR), Nowomiejska, Katarzyna^3,4 (AUTHOR), Kuehlewein, Laura^1,3 (AUTHOR), Kohl, Susanne³ (AUTHOR), Kempf, Melanie^1,2 (AUTHOR), Strasser, Torsten³ (AUTHOR), Jung, Ronja¹ (AUTHOR), Wilhelm, Barbara⁵ (AUTHOR), Peters, Tobias^3,5 (AUTHOR), Kelbsch, Carina¹ (AUTHOR), Bartz-Schmidt, Karl Ulrich¹ (AUTHOR), Langrova, Hana⁶ (AUTHOR), Zrenner, Eberhart^1,2,3,7 (AUTHOR)

Publikováno v: Ophthalmologica. 2021, Vol. 244 Issue 5, p396-407. 12p.

Central retina plays a decisive role in the suppression of pupillary escape.

Autor: Kelbsch, Carina^1,2 (AUTHOR), Jendritza, Ricarda² (AUTHOR), Strasser, Torsten^1,2,3 (AUTHOR), Tonagel, Felix¹ (AUTHOR), Richter, Paul^1,2 (AUTHOR), Jung, Ronja^1,2 (AUTHOR), Peters, Tobias² (AUTHOR), Wilhelm, Helmut^1,2 (AUTHOR), Wilhelm, Barbara² (AUTHOR) Barbara.wilhelm@stz-eyetrial.de, Stingl, Krunoslav^1,2,4 (AUTHOR)

Publikováno v: Graefe's Archive of Clinical & Experimental Ophthalmology. Jun2023, Vol. 261 Issue 6, p1713-1722. 10p.

Evaluation of Local Rod and Cone Function in Stargardt Disease

Autor: Stingl, Krunoslav, Hoyng, Carel, Kempf, Melanie, Kohl, Susanne, Jung, Ronja, Righetti, Giulia, Kühlewein, Laura, Pohl, Lisa, Kortüm, Friederike, Kelbsch, Carina, Wilhelm, Barbara, Peters, Tobias, Stingl, Katarina, on behalf of the SORAPRAZAN consortium

PURPOSE. In this study, chromatic pupil campimetry (CPC) was used to map local functional degenerative changes of cones and rods in Stargardt disease (STGD1). METHODS. 19 patients (age 36 ± 8 years; 12 males) with genetically confirmed ABCA4 mutatio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2659::8895780806b462758b5406dafce7a938
https://zenodo.org/record/6347175

Evaluation of Local Rod and Cone Function in Stargardt Disease

Publikováno v: Investigative Ophthalmology and Visual Science. 63(3)

PURPOSE. In this study, chromatic pupil campimetry (CPC) was used to map local functional degenerative changes of cones and rods in Stargardt disease (STGD1). METHODS. 19 patients (age 36 ± 8 years; 12 males) with genetically confirmed ABCA4 mutatio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dris___00893::8e0c2b039d21c18171aff93f685600db
https://doi.org/10.1167/iovs.63.3.6