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Markus N Preising

Showing results (21-30 of 47) with videos related to

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Ophthalmology|August 4, 2004
Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65Birgit Lorenz, Bettina Wabbels, Erika Wegscheider, et al.
Investigative Ophthalmology & Visual Science|July 5, 2008
A comprehensive clinical and biochemical functional study of a novel RPE65 hypomorphic mutationBirgit Lorenz, Eugenia Poliakov, Maria Schambeck, et al.
Investigative Ophthalmology & Visual Science|April 26, 2012
Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophyMarkus N Preising, Nora Hausotter-Will, Manuel C Solbach, et al.
Ophthalmology|April 21, 2009
Fundus autofluorescence in carriers of choroideremia and correlation with electrophysiologic and psychophysical dataMarkus N Preising, Erika Wegscheider, Christoph Friedburg, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 23, 2002
Phenotypes of 16 Stargardt macular dystrophy/fundus flavimaculatus patients with known ABCA4 mutations and evaluation of genotype-phenotype correlationChristina Gerth, Monika Andrassi-Darida, Markus Bock, et al.
Clinical Ophthalmology (Auckland, N.Z.)|December 10, 2016
Rebound macular edema following oral acetazolamide therapy for juvenile X-linked retinoschisis in an Italian familyMaria Silvana Galantuomo, Maurizio Fossarello, Alberto Cuccu, et al.
Investigative Ophthalmology & Visual Science|June 6, 2013
Automated segmentation of pathological cavities in optical coherence tomography scansMatthäus Pilch, Knut Stieger, Yaroslava Wenner, 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 SettingBirgit Lorenz, Sandrine H Künzel, Markus N Preising, et al.
Molecular Vision|October 26, 2007
Mutation analysis in a family with oculocutaneous albinism manifesting in the same generation of three branchesMarkus N Preising, Hedwig Forster, H Tan, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|December 11, 2025
Chorioretinal Atrophy after Voretigene Neparvovec Therapy in <italic>RPE65</italic> Mutation-Associated Inherited Retinal Disease: Longitudinal Characterization in Multimodal ImagingSandrine H Sassen, Marlene Sassmannshausen, Josua Sassen, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Ophthalmology|August 4, 2004
Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65Birgit Lorenz, Bettina Wabbels, Erika Wegscheider, et al.
Investigative Ophthalmology & Visual Science|July 5, 2008
A comprehensive clinical and biochemical functional study of a novel RPE65 hypomorphic mutationBirgit Lorenz, Eugenia Poliakov, Maria Schambeck, et al.
Investigative Ophthalmology & Visual Science|April 26, 2012
Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophyMarkus N Preising, Nora Hausotter-Will, Manuel C Solbach, et al.
Ophthalmology|April 21, 2009
Fundus autofluorescence in carriers of choroideremia and correlation with electrophysiologic and psychophysical dataMarkus N Preising, Erika Wegscheider, Christoph Friedburg, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 23, 2002
Phenotypes of 16 Stargardt macular dystrophy/fundus flavimaculatus patients with known ABCA4 mutations and evaluation of genotype-phenotype correlationChristina Gerth, Monika Andrassi-Darida, Markus Bock, et al.
Clinical Ophthalmology (Auckland, N.Z.)|December 10, 2016
Rebound macular edema following oral acetazolamide therapy for juvenile X-linked retinoschisis in an Italian familyMaria Silvana Galantuomo, Maurizio Fossarello, Alberto Cuccu, et al.
Investigative Ophthalmology & Visual Science|June 6, 2013
Automated segmentation of pathological cavities in optical coherence tomography scansMatthäus Pilch, Knut Stieger, Yaroslava Wenner, 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 SettingBirgit Lorenz, Sandrine H Künzel, Markus N Preising, et al.
Molecular Vision|October 26, 2007
Mutation analysis in a family with oculocutaneous albinism manifesting in the same generation of three branchesMarkus N Preising, Hedwig Forster, H Tan, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|December 11, 2025
Chorioretinal Atrophy after Voretigene Neparvovec Therapy in <italic>RPE65</italic> Mutation-Associated Inherited Retinal Disease: Longitudinal Characterization in Multimodal ImagingSandrine H Sassen, Marlene Sassmannshausen, Josua Sassen, et al.
Pageof 5