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Silke Weinitz

Showing results (11-20 of 18) with videos related to

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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.
American Journal of Ophthalmology|February 27, 2009
Lipofuscin- and melanin-related fundus autofluorescence in patients with ABCA4-associated retinal dystrophiesSimone Kellner, Ulrich Kellner, Bernhard H F Weber, et al.
Klinische Monatsblatter Fur Augenheilkunde|August 21, 2015
[Macular Spectral Domain Optical Coherence Tomography: Clinical Evaluation]Ulrich Kellner, Simone Kellner, Azadeh Golshahi, 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.
Ophthalmic Genetics|January 16, 2016
Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1Simone Kellner, Heidi Stöhr, Britta Fiebig, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 23, 2021
Treatment contentment and preference of patients undergoing intravitreal anti-VEGF therapyUlrich Kellner, Mohammad Seleman Bedar, Silke Weinitz, et al.
International Journal of Molecular Sciences|March 6, 2021
Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel <i>C1QTNF5</i> Missense VariantUlrich Kellner, Nicole Weisschuh, Silke Weinitz, et al.
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Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
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.
American Journal of Ophthalmology|February 27, 2009
Lipofuscin- and melanin-related fundus autofluorescence in patients with ABCA4-associated retinal dystrophiesSimone Kellner, Ulrich Kellner, Bernhard H F Weber, et al.
Klinische Monatsblatter Fur Augenheilkunde|August 21, 2015
[Macular Spectral Domain Optical Coherence Tomography: Clinical Evaluation]Ulrich Kellner, Simone Kellner, Azadeh Golshahi, 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.
Ophthalmic Genetics|January 16, 2016
Fundus Autofluorescence and SD-OCT Document Rapid Progression in Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Associated with a c.256G > A Mutation in BEST1Simone Kellner, Heidi Stöhr, Britta Fiebig, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 23, 2021
Treatment contentment and preference of patients undergoing intravitreal anti-VEGF therapyUlrich Kellner, Mohammad Seleman Bedar, Silke Weinitz, et al.
International Journal of Molecular Sciences|March 6, 2021
Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel <i>C1QTNF5</i> Missense VariantUlrich Kellner, Nicole Weisschuh, Silke Weinitz, et al.
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