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Christoph Friedburg

Showing results (1-10 of 24) with videos related to

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Investigative Ophthalmology & Visual Science|May 30, 2013
Improving detection of mild loss of retinal light increment sensitivity at the posterior pole with the microperimeter MP1Wadim Bowl, Birgit Lorenz, Melanie Jäger, et al.
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.
Investigative Ophthalmology & Visual Science|September 14, 2011
Long-term follow-up of the human phenotype in three siblings with cone dystrophy associated with a homozygous p.G461R mutation of KCNV2Christoph Friedburg, Bernd Wissinger, Maria Schambeck, 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.
Vision Research|June 5, 2002
Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein typeHana Langrová, Daphne Gamer, Christoph Friedburg, et al.
Investigative Ophthalmology & Visual Science|July 19, 2012
Chromatic pupillometry dissects function of the three different light-sensitive retinal cell populations in RPE65 deficiencyBirgit Lorenz, Elisabeth Strohmayr, Steffen Zahn, 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.
Die Ophthalmologie|April 21, 2023
[10 years of screening for retinopathy of prematurity (2009-2019) : Results analysis of two German level-1 neonatal intensive care units (NICUs) with university on-site screening and a telemedical approach in the non-university NICU]Valentina Busik, Birgit Lorenz, Christine Mais, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Investigative Ophthalmology & Visual Science|May 30, 2013
Improving detection of mild loss of retinal light increment sensitivity at the posterior pole with the microperimeter MP1Wadim Bowl, Birgit Lorenz, Melanie Jäger, et al.
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.
Investigative Ophthalmology & Visual Science|September 14, 2011
Long-term follow-up of the human phenotype in three siblings with cone dystrophy associated with a homozygous p.G461R mutation of KCNV2Christoph Friedburg, Bernd Wissinger, Maria Schambeck, 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.
Vision Research|June 5, 2002
Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein typeHana Langrová, Daphne Gamer, Christoph Friedburg, et al.
Investigative Ophthalmology & Visual Science|July 19, 2012
Chromatic pupillometry dissects function of the three different light-sensitive retinal cell populations in RPE65 deficiencyBirgit Lorenz, Elisabeth Strohmayr, Steffen Zahn, 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.
Die Ophthalmologie|April 21, 2023
[10 years of screening for retinopathy of prematurity (2009-2019) : Results analysis of two German level-1 neonatal intensive care units (NICUs) with university on-site screening and a telemedical approach in the non-university NICU]Valentina Busik, Birgit Lorenz, Christine Mais, et al.
Pageof 3