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Eye (London, England)
|
October 30, 2024
Age-related macular degeneration: natural history revisited in geographic atrophy
Eliza Broadbent, Sandrine H Künzel, Maximilian Pfau, et al.
Die Ophthalmologie
|
August 15, 2023
[Diagnostics and management of patients with inherited retinal diseases in Germany : Results of a nationwide survey of university and non-university eye departments and specialized practices]
Sandrine H Künzel, Elias Mahren, Mitjan Morr, et al.
Journal of Clinical Medicine
|
June 27, 2024
Optic Disc Drusen in Pseudoxanthoma Elasticum Are Associated with the Extent of Bruch's Membrane Calcification
Kristin Raming, Sandrine H Künzel, Maximilian Pfau, et al.
Acta Ophthalmologica
|
November 7, 2023
Multimodal imaging and deep learning in geographic atrophy secondary to age-related macular degeneration
Maximilian Pfau, Sandrine H Künzel, Kristina Pfau, et al.
Die Ophthalmologie
|
November 14, 2025
[Ophthalmological care of patients with Bardet-Biedl syndrome]
Elisa A Mahler, Constanze L Kochs, Marlene Saßmannshausen, et al.
Ophthalmology
|
September 13, 2023
Single Center Experience with Voretigene Neparvovec Gene Augmentation Therapy in RPE65 Mutation-Associated Inherited Retinal Degeneration in a Clinical Setting
Birgit Lorenz, Sandrine H Künzel, Markus N Preising, et al.
European Journal of Ophthalmology
|
January 24, 2024
Transcriptome Analysis of Choroidal Endothelium Links Androgen Receptor Role to Central Serous Chorioretinopathy
Sandrine H Künzel, Dominika Pohlmann, Lynn Zur Bonsen, et al.
Investigative Ophthalmology & Visual Science
|
January 2, 2025
Deep Learning-Based SD-OCT Layer Segmentation Quantifies Outer Retina Changes in Patients With Biallelic RPE65 Mutations Undergoing Gene Therapy
German Pinedo-Diaz, Birgit Lorenz, Sandrine H Künzel, et al.
American Journal of Ophthalmology Case Reports
|
March 19, 2025
Phenotypic characterization of a female patient with retinitis pigmentosa caused by a homozygous X-linked <i>RPGR</i> <sup></sup> mutation
Marlene Saßmannshausen, Elisa A Mahler, Sandrine H Künzel, et al.
Circulation
|
July 7, 2018
SMAD4 Prevents Flow Induced Arteriovenous Malformations by Inhibiting Casein Kinase 2
Roxana Ola, Sandrine H Künzel, Feng Zhang, et al.
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Search research articles
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Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Eye (London, England)
|
October 30, 2024
Age-related macular degeneration: natural history revisited in geographic atrophy
Eliza Broadbent, Sandrine H Künzel, Maximilian Pfau, et al.
Die Ophthalmologie
|
August 15, 2023
[Diagnostics and management of patients with inherited retinal diseases in Germany : Results of a nationwide survey of university and non-university eye departments and specialized practices]
Sandrine H Künzel, Elias Mahren, Mitjan Morr, et al.
Journal of Clinical Medicine
|
June 27, 2024
Optic Disc Drusen in Pseudoxanthoma Elasticum Are Associated with the Extent of Bruch's Membrane Calcification
Kristin Raming, Sandrine H Künzel, Maximilian Pfau, et al.
Acta Ophthalmologica
|
November 7, 2023
Multimodal imaging and deep learning in geographic atrophy secondary to age-related macular degeneration
Maximilian Pfau, Sandrine H Künzel, Kristina Pfau, et al.
Die Ophthalmologie
|
November 14, 2025
[Ophthalmological care of patients with Bardet-Biedl syndrome]
Elisa A Mahler, Constanze L Kochs, Marlene Saßmannshausen, et al.
Ophthalmology
|
September 13, 2023
Single Center Experience with Voretigene Neparvovec Gene Augmentation Therapy in RPE65 Mutation-Associated Inherited Retinal Degeneration in a Clinical Setting
Birgit Lorenz, Sandrine H Künzel, Markus N Preising, et al.
European Journal of Ophthalmology
|
January 24, 2024
Transcriptome Analysis of Choroidal Endothelium Links Androgen Receptor Role to Central Serous Chorioretinopathy
Sandrine H Künzel, Dominika Pohlmann, Lynn Zur Bonsen, et al.
Investigative Ophthalmology & Visual Science
|
January 2, 2025
Deep Learning-Based SD-OCT Layer Segmentation Quantifies Outer Retina Changes in Patients With Biallelic RPE65 Mutations Undergoing Gene Therapy
German Pinedo-Diaz, Birgit Lorenz, Sandrine H Künzel, et al.
American Journal of Ophthalmology Case Reports
|
March 19, 2025
Phenotypic characterization of a female patient with retinitis pigmentosa caused by a homozygous X-linked <i>RPGR</i> <sup></sup> mutation
Marlene Saßmannshausen, Elisa A Mahler, Sandrine H Künzel, et al.
Circulation
|
July 7, 2018
SMAD4 Prevents Flow Induced Arteriovenous Malformations by Inhibiting Casein Kinase 2
Roxana Ola, Sandrine H Künzel, Feng Zhang, et al.
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