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Journal of Clinical Medicine|November 27, 2024
Near-Infrared Autofluorescence: Early Detection of Retinal Pigment Epithelial Alterations in Inherited Retinal DystrophiesSimone Kellner, Silke Weinitz, Ghazaleh Farmand, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|February 18, 2025
The value of genetic testing in pediatric and adult ophthalmologyUlrich Kellner, Simone Kellner, Silke Weinitz, et al.
The British Journal of Ophthalmology|November 5, 2013
Cystoid macular oedema and epiretinal membrane formation during progression of chloroquine retinopathy after drug cessationSimone Kellner, Silke Weinitz, Ghazaleh Farmand, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|November 19, 2020
[Toxic retinopathies]Ulrich Kellner, Simone Kellner, Silke Weinitz, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 24, 2022
[Near-infrared Fundus Autofluorescence: Clinical Application and Diagnostic Relevance]Simone Kellner, Silke Weinitz, Ghazaleh Farmand, et al.
Klinische Monatsblatter Fur Augenheilkunde|November 17, 2022
[Exogenously induced retinopathies]Ulrich Kellner, Simone Kellner, Silke Weinitz, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 4, 2022
Optical coherence tomography angiography (OCT-A) in retinitis pigmentosa and macular dystrophy patients: a retrospective studySebastian Deutsch, Albrecht Lommatzsch, Silke Weinitz, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 18, 2020
[Congenital Retinal Dystrophies: Combining Ophthalmological Techniques to Improve the Read-out]Ulrich Kellner, Simone Kellner, Mohammad Saleh, et al.
Ophthalmic Genetics|January 18, 2017
Mevalonate kinase deficiency associated with ataxia and retinitis pigmentosa in two brothers with MVK gene mutationsUlrich Kellner, Heidi Stöhr, Silke Weinitz, et al.
Journal of Clinical Medicine|July 29, 2025
Bilateral Sector Macular Dystrophy Associated with <i>PRPH2</i> Variant c.623G>A (p.Gly208Asp)Simone Kellner, Silke Weinitz, Ghazaleh Farmand, et al.
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