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Markus N Preising

Showing results (1-10 of 47) with videos related to

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Trends in Molecular Medicine|April 27, 2004
Recent advances in early-onset severe retinal degeneration: more than just basic researchMarkus N Preising, Steffen Heegaard
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 23, 2004
Age matters--thoughts on a grading system for ABCA4 mutationsBirgit Lorenz, Markus N Preising
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 3, 2004
Fundus autofluorescence in carriers of X-linked recessive retinitis pigmentosa associated with mutations in RPGR, and correlation with electrophysiological and psychophysical dataErika Wegscheider, Markus N Preising, Birgit Lorenz
Vision Research|November 13, 2003
Analysis of three genes in Leber congenital amaurosis in Indonesian patientsRita S Sitorus, Birgit Lorenz, Markus N Preising
Klinische Monatsblatter Fur Augenheilkunde|February 2, 2018
[Overview of Congenital Stationary Night Blindness with Predominantly Normal Fundus Appearance]Christina Zeitz, Christoph Friedburg, Markus N Preising, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 8, 2019
Splitting of the lateral rectus muscle with medial transposition to treat oculomotor palsy: a retrospective analysis of 29 consecutive casesSotirios Basiakos, Michael Gräf, Markus N Preising, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|November 27, 2004
Longitudinal and cross-sectional study of patients with early-onset severe retinal dystrophy associated with RPE65 mutationsKarina Paunescu, Bettina Wabbels, Markus N Preising, et al.
Molecular Vision|May 5, 2011
Screening of TYR, OCA2, GPR143, and MC1R in patients with congenital nystagmus, macular hypoplasia, and fundus hypopigmentation indicating albinismMarkus N Preising, Hedwig Forster, Miriam Gonser, et al.
Ophthalmic Genetics|December 17, 2013
Bestrophin 1--Phenotypes and Functional Aspects in BestrophinopathiesCaroline Pasquay, Lu Fei Wang, Birgit Lorenz, et al.
European Journal of Human Genetics : EJHG|February 13, 2014
Clinical utility gene card for: Oculocutaneous albinismKaren Grønskov, Karen Brøndum-Nielsen, Birgit Lorenz, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Trends in Molecular Medicine|April 27, 2004
Recent advances in early-onset severe retinal degeneration: more than just basic researchMarkus N Preising, Steffen Heegaard
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 23, 2004
Age matters--thoughts on a grading system for ABCA4 mutationsBirgit Lorenz, Markus N Preising
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 3, 2004
Fundus autofluorescence in carriers of X-linked recessive retinitis pigmentosa associated with mutations in RPGR, and correlation with electrophysiological and psychophysical dataErika Wegscheider, Markus N Preising, Birgit Lorenz
Vision Research|November 13, 2003
Analysis of three genes in Leber congenital amaurosis in Indonesian patientsRita S Sitorus, Birgit Lorenz, Markus N Preising
Klinische Monatsblatter Fur Augenheilkunde|February 2, 2018
[Overview of Congenital Stationary Night Blindness with Predominantly Normal Fundus Appearance]Christina Zeitz, Christoph Friedburg, Markus N Preising, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 8, 2019
Splitting of the lateral rectus muscle with medial transposition to treat oculomotor palsy: a retrospective analysis of 29 consecutive casesSotirios Basiakos, Michael Gräf, Markus N Preising, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|November 27, 2004
Longitudinal and cross-sectional study of patients with early-onset severe retinal dystrophy associated with RPE65 mutationsKarina Paunescu, Bettina Wabbels, Markus N Preising, et al.
Molecular Vision|May 5, 2011
Screening of TYR, OCA2, GPR143, and MC1R in patients with congenital nystagmus, macular hypoplasia, and fundus hypopigmentation indicating albinismMarkus N Preising, Hedwig Forster, Miriam Gonser, et al.
Ophthalmic Genetics|December 17, 2013
Bestrophin 1--Phenotypes and Functional Aspects in BestrophinopathiesCaroline Pasquay, Lu Fei Wang, Birgit Lorenz, et al.
European Journal of Human Genetics : EJHG|February 13, 2014
Clinical utility gene card for: Oculocutaneous albinismKaren Grønskov, Karen Brøndum-Nielsen, Birgit Lorenz, et al.
Pageof 5