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Markus N Preising

Showing results (11-20 of 47) with videos related to

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Klinische Monatsblatter Fur Augenheilkunde|March 22, 2019
[Reduced Visual Acuity at the Age of 3 Years and Flat Unilateral Retinal Detachment at the Age of 9 Years - History of a Child with Compound Heterozygous RP1 Mutations]Daniela Aneta Starosta, Birgit Lorenz, Lyubomyr Lytvynchuk, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 3, 2006
Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in PJochen Graw, Norman Klopp, Thomas Illig, et al.
Ophthalmic Research|July 12, 2017
Spatially Resolved Spectral Sensitivities as a Potential Read-out Parameter in Clinical Gene Therapeutic TrialsBirgit Lorenz, Erika Wegscheider, Christian Hamel, et al.
Ophthalmic Research|August 18, 2015
Shared decision-making, control preferences and psychological well-being in patients with RPE65 deficiency awaiting experimental gene therapyMonika Nelles, Knut Stieger, Markus N Preising, et al.
Ophthalmic Genetics|August 4, 2016
Ocular morphology and function in juvenile neuronal ceroid lipofuscinosis (CLN3) in the first decade of lifeMarkus N Preising, Michaela Abura, Melanie Jäger, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 25, 2003
[On the effect of mutations of the fibroblast growth factor receptors as exemplified by three cases of craniosynostoses]Markus N Preising, Sabine Schindler, Monika Friedrich, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 22, 2019
[The Phenotypic Spectrum of Ophthalmic Changes in CEP290 Mutations]Markus N Preising, Ute Schneider, Christoph Friedburg, et al.
Ophthalmic Epidemiology|May 14, 2013
Prevalence and diagnostic spectrum of generalized retinal dystrophy in Danish childrenMette Bertelsen, Hanne Jensen, Michael Larsen, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 22, 2005
Fundus autofluorescence in children and teenagers with hereditary retinal diseasesBettina Wabbels, Anke Demmler, Karina Paunescu, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 12, 2014
Normative values of peripheral retinal thickness measured with Spectralis OCT in healthy young adultsYaroslava Wenner, Stephan Wismann, Markus N Preising, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Klinische Monatsblatter Fur Augenheilkunde|March 22, 2019
[Reduced Visual Acuity at the Age of 3 Years and Flat Unilateral Retinal Detachment at the Age of 9 Years - History of a Child with Compound Heterozygous RP1 Mutations]Daniela Aneta Starosta, Birgit Lorenz, Lyubomyr Lytvynchuk, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 3, 2006
Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in PJochen Graw, Norman Klopp, Thomas Illig, et al.
Ophthalmic Research|July 12, 2017
Spatially Resolved Spectral Sensitivities as a Potential Read-out Parameter in Clinical Gene Therapeutic TrialsBirgit Lorenz, Erika Wegscheider, Christian Hamel, et al.
Ophthalmic Research|August 18, 2015
Shared decision-making, control preferences and psychological well-being in patients with RPE65 deficiency awaiting experimental gene therapyMonika Nelles, Knut Stieger, Markus N Preising, et al.
Ophthalmic Genetics|August 4, 2016
Ocular morphology and function in juvenile neuronal ceroid lipofuscinosis (CLN3) in the first decade of lifeMarkus N Preising, Michaela Abura, Melanie Jäger, et al.
Klinische Monatsblatter Fur Augenheilkunde|October 25, 2003
[On the effect of mutations of the fibroblast growth factor receptors as exemplified by three cases of craniosynostoses]Markus N Preising, Sabine Schindler, Monika Friedrich, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 22, 2019
[The Phenotypic Spectrum of Ophthalmic Changes in CEP290 Mutations]Markus N Preising, Ute Schneider, Christoph Friedburg, et al.
Ophthalmic Epidemiology|May 14, 2013
Prevalence and diagnostic spectrum of generalized retinal dystrophy in Danish childrenMette Bertelsen, Hanne Jensen, Michael Larsen, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 22, 2005
Fundus autofluorescence in children and teenagers with hereditary retinal diseasesBettina Wabbels, Anke Demmler, Karina Paunescu, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 12, 2014
Normative values of peripheral retinal thickness measured with Spectralis OCT in healthy young adultsYaroslava Wenner, Stephan Wismann, Markus N Preising, et al.
Pageof 5