Anzahl der Publikationen: 11
2022
2021
Schworm, Benedikt; Luft, Nikolaus; Keidel, Leonie F.; Kreutzer, Thomas C.; Herold, Tina R.; Priglinger, Siegfried G. und Siedlecki, Jakob
(2021):
Vanishing pachy-choroid in pachychoroid neovasculopathy under long-term anti-vascular endothelial growth factor therapy.
In: BMC ophthalmology, Bd. 21, Nr. 1, 269
[PDF, 786kB]
Keidel, Leonie F.; Zwingelberg, Sarah; Schworm, Benedikt; Luft, Nikolaus; Herold, Tina; Priglinger, Siegfried G. und Siedlecki, Jakob
(2021):
Pachychoroid disease and its association with retinal vein occlusion: a case-control study.
In: Scientific reports, Bd. 11, 19854
[PDF, 1MB]
Keidel, Leonie F.; Zwingelberg, Sarah; Schworm, Benedikt; Luft, Nikolaus; Herold, Tina; Priglinger, Siegfried G. und Siedlecki, Jakob
(2021):
Pachychoroid disease and its association with retinal vein occlusion: a case-control study.
In: Scientific Reports, Bd. 11, Nr. 1, 19854
Schworm, Benedikt; Luft, Nikolaus; Keidel, Leonie F.; Kreutzer, Thomas C.; Herold, Tina R.; Priglinger, Siegfried G. und Siedlecki, Jakob
(2021):
Vanishing pachy-choroid in pachychoroid neovasculopathy under long-term anti-vascular endothelial growth factor therapy.
In: BMC Ophthalmology, Bd. 21, Nr. 1, 269
2020
Schworm, Benedikt; Luft, Nikolaus; Keidel, Leonie F.; Hagenau, Felix; Kern, Christoph; Herold, Tina; Kortüm, Karsten U.; Priglinger, Siegfried G. und Siedlecki, Jakob
(2020):
Response of neovascular central serous chorioretinopathy to an extended upload of anti-VEGF agents.
In: Graefe's Archive for Clinical and Experimental Ophthalmology, Bd. 258: S. 1013-1021
[PDF, 761kB]
Schworm, Benedikt; Luft, Nikolaus; Keidel, Leonie F.; Herold, Tina R.; Wolf, Armin; Priglinger, Siegfried G. und Siedlecki, Jakob
(2020):
Ranibizumab non-response in pachychoroid neovasculopathy: Effects of switching to aflibercept.
In: Scientific Reports, Bd. 10, Nr. 1, 8439
[PDF, 1MB]
Radelfahr, Florentine; Riedhammer, Korbinian M.; Keidel, Leonie F.; Gramer, Gwendolyn; Meitinger, Thomas; Klopstock, Thomas und Wagner, Matias
(2020):
Biotinidase deficiency: A treatable cause of hereditary spastic paraparesis.
In: Neurology-Genetics, Bd. 6, Nr. 6, e525
[PDF, 187kB]
Diese Liste wurde am
Sun Nov 24 00:18:35 2024 CET
erstellt.