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Articles December 2019

Chromatic Full-Field Stimulus Threshold and Pupillography as Functional Markers for Late-Stage, Early-Onset Retinitis Pigmentosa Caused by CRB1 Mutations

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Krunoslav T. Stingl; Laura Kuehlewein; Nicole Weisschuh; Saskia Biskup; Frans P. M. Cremers; M. Imran Khan; Carina Kelbsch; Tobias Peters; Marius Ueffing; Barbara Wilhelm; Eberhart Zrenner; Katarina Stingl
TAGS: eye, illness length, mutation, pupil reaction, retinitis pigmentosa
Trans. Vis. Sci. Tech.. 2019; 8(6):45. doi: https://doi.org/10.1167/tvst.8.6.45

ARVO Annual Meeting Abstract July 2019

Does close work affect the ciliary muscle morphology?

Sandra Wagner; Frank Schaeffel; Eberhart Zrenner; Torsten Strasser

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1399. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2019

Evaluation of pupil responses to local stimuli in Patients with retinitis pigmentosa caused by USH2A mutations

Tobias Peters; Krunoslav Stingl; Karl Ulrich Bartz-Schmidt; Laura Kuehlewein; Carina Kelbsch; Melanie Kempf; Eberhart Zrenner; Barbara Wilhelm; Katarina Stingl

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1829. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2019

Selective activation of ON and OFF RGC input in mouse retina stimulated

Zohreh Hosseinzadeh; Daniel Llewellyn Rathbun; Eberhart Zrenner

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4989. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2019

PARP inhibitors: The protective ways on retinal degeneration

Ayse Sahaboglu; maria miranda; Serdar Durdagi; Gulru Kayik; Eberhart Zrenner

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5177. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2019

Multi-Electrode-Recording for classification of retinal ganglion cells for bionic vision: comparison with calcium imaging responses.

hamed shabani; Mahdi Sadeghi; Zohreh Hosseinzadeh; Eberhart Zrenner; Daniel Llewellyn Rathbun

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5283. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2019

Effects of Subretinal AAV8 Gene Therapy on Microperimetry in CNGA3 Achromatopsia Patients

G. Alex Ochakovski; Ahmad Zhour; Laura Kuehlewein; Susanne Kohl; Andrea Rindtorff; Karl Ulrich Bartz-Schmidt; Marius Ueffing; Eberhart Zrenner; Stylianos Michalakis; Martin Biel; Bernd Wissinger; Tobias Peters; Barbara Wilhelm; M. Dominik Fischer

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2921. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2018

Can you see the panda? Visual acuity assessment using the pandacuity test in children – preliminary results

Torsten Strasser; Bettina Spieth; Eberhart Zrenner; Dorothea Besch; Carina Kelbsch

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5199. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2018

Phenotypic heterogeneity of retinal degenerations caused by mutations in CRX examined by multimodal clinical imaging including adaptive optics retinal camera

Katarina Stingl; Laura Kuehlewein; Melanie Kempf; Francoise Sadler; Fadi Nasser; Bernd Wissinger; Susanne Kohl; Nicole Weisschuh; Marius Ueffing; Eberhart Zrenner

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1516. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2018

Ciliary muscle thickness profiles in far and near accommodation

Sandra Wagner; Torsten Strasser; Eberhart Zrenner

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2940. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2018

First Gene Supplementation Therapy for CNGA3-linked Achromatopsia

M Dominik Fischer; Stylianos Michalakis; Barbara Wilhelm; Nadine Kahle; Tobias Peters; Karl Ulrich Bartz-Schmidt; Susanne Kohl; Mathias W Seeliger; Nicole Weisschuh; Ditta Zobor; Eberhart Zrenner; Marius Ueffing; Martin Biel; Bernd Wissinger

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2982. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2018

Changes in Microchip Position after Implantation of a Subretinal Vision Prosthesis in Humans

Laura Kuehlewein; Nicole Troelenberg; Krunoslav Stingl; Sebastian Schleehauf; Akos Kusnyerik; Helmut Sachs; Johann Roider; Timothy L Jackson; Robert E MacLaren; Caroline Chee; Barbara Wilhelm; Florian Gekeler; Karl Ulrich Bartz-Schmidt; Eberhart Zrenner; Katarina Stingl

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):4561. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2018

Progression of Stargardt disease as measured by spectral-domain optical coherence tomography (SD-OCT) in the ProgStar Study

Rupert Wolfgang Strauss; Xiangrong Kong; Beatriz E Munoz; Sheila K West; Michael S Ip; Alexander Ho; Anamika Jha; Paul S Bernstein; David G Birch; Artur V Cideciyan; Michel Michaelides; José-Alain Sahel; Janet S Sunness; Elias I Traboulsi; Eberhart Zrenner; Hendrik P Scholl

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1568. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2018

CEP290 mutation spectrum in Germany and delineation of the associated phenotype

Ditta Zobor; Britta Feldhaus; Nicole Weisschuh; Fadi Nasser; Eberhart Zrenner; Susanne Kohl

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):23. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2018

Olfactory dysfunction in patients with CNGB1 -related retinitis pigmentosa

Peter Charbel Issa; Peggy Reuter; Laura Kuehlewein; Johannes Birtel; Martin Gliem; Anke Tropitzsch; Katherine Whitcroft; Hanno Bolz; Kenji Ishihara; Robert E MacLaren; Susan Downes; Akio Oishi; Eberhart Zrenner; Susanne Kohl; Thomas Hummel

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1565. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2018

Leber congenital amaurosis (LCA): Prevalence of mutations in a large German cohort and clinical characterization of the associated phenotype

Britta Feldhaus; Susanne Kohl; Nicole Weisschuh; Fadi Nasser; Eberhart Zrenner; Ditta Zobor

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1832. doi: https://doi.org/

Retina June 2018

Phenotype Variations Caused by Mutations in the RP1L1 Gene in a Large Mainly German Cohort

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Ditta Zobor; Gergely Zobor; Stephanie Hipp; Britta Baumann; Nicole Weisschuh; Saskia Biskup; Ieva Sliesoraityte; Eberhart Zrenner; Susanne Kohl
TAGS: cohort studies, genes, german, mutation, phenotype, spectral-domain optical coherence tomography, heterozygote, electroretinography
Invest. Ophthalmol. Vis. Sci.. 2018; 59(7):3041-3052. doi: https://doi.org/10.1167/iovs.18-24033

Retina November 2017

Superior Retinal Gene Transfer and Biodistribution Profile of Subretinal Versus Intravitreal Delivery of AAV8 in Nonhuman Primates

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Immanuel P. Seitz; Stylianos Michalakis; Barbara Wilhelm; Felix F. Reichel; G. Alex Ochakovski; Eberhart Zrenner; Marius Ueffing; Martin Biel; Bernd Wissinger; Karl U. Bartz-Schmidt; Tobias Peters; M. Dominik Fischer; for the RD-CURE Consortium
TAGS: cohort studies, disease vectors, dna, gene transfer techniques, genome, injections, primates, spatial vectors, body tissue, surgical procedures, operative
Invest. Ophthalmol. Vis. Sci.. 2017; 58(13):5792-5801. doi: https://doi.org/10.1167/iovs.17-22473

Includes: Supplemental Content

Retina September 2017

High Symmetry of Visual Acuity and Visual Fields in RPGR -Linked Retinitis Pigmentosa

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Julia-Sophia Bellingrath; G. Alex Ochakovski; Immanuel P. Seitz; Susanne Kohl; Eberhart Zrenner; Nicola Hanig; Holger Prokisch; Bernhard H. Weber; Susan M. Downes; Simon Ramsden; Robert E. MacLaren; M. Dominik Fischer
TAGS: cohort studies, disease progression, electroretinography, eye, mutation, phenotype, retinitis pigmentosa, visual acuity, visual fields, vision
Invest. Ophthalmol. Vis. Sci.. 2017; 58(11):4457-4466. doi: https://doi.org/10.1167/iovs.17-22077

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2017

Results from a Multicenter Trial with the New Electronic Subretinal Implant Alpha AMS in 15 Patients Blind from Inherired Retinal Dystrophies (RD)

Eberhart Zrenner; Karl-Ulrich Bartz-Schmidt; Charles L Cottriall; Thomas Edwards; Florian Gekeler; Udo Greppmaier; Laura Kuehlewein; Robert E MacLaren; James Ramsden; Johann Roider; Helmut G Sachs; Ruth Schippert; Jan Tode; Nicole Troelenberg; Katarina Stingl

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4266. doi: https://doi.org/

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Chromatic Full-Field Stimulus Threshold and Pupillography as Functional Markers for Late-Stage, Early-Onset Retinitis Pigmentosa Caused by CRB1 Mutations

Does close work affect the ciliary muscle morphology?

Evaluation of pupil responses to local stimuli in Patients with retinitis pigmentosa caused by USH2A mutations

Selective activation of ON and OFF RGC input in mouse retina stimulated

PARP inhibitors: The protective ways on retinal degeneration

Multi-Electrode-Recording for classification of retinal ganglion cells for bionic vision: comparison with calcium imaging responses.

Effects of Subretinal AAV8 Gene Therapy on Microperimetry in CNGA3 Achromatopsia Patients

Can you see the panda? Visual acuity assessment using the pandacuity test in children – preliminary results

Phenotypic heterogeneity of retinal degenerations caused by mutations in CRX examined by multimodal clinical imaging including adaptive optics retinal camera

Ciliary muscle thickness profiles in far and near accommodation

First Gene Supplementation Therapy for CNGA3-linked Achromatopsia

Changes in Microchip Position after Implantation of a Subretinal Vision Prosthesis in Humans

Progression of Stargardt disease as measured by spectral-domain optical coherence tomography (SD-OCT) in the ProgStar Study

CEP290 mutation spectrum in Germany and delineation of the associated phenotype

Olfactory dysfunction in patients with CNGB1 -related retinitis pigmentosa

Leber congenital amaurosis (LCA): Prevalence of mutations in a large German cohort and clinical characterization of the associated phenotype

Phenotype Variations Caused by Mutations in the RP1L1 Gene in a Large Mainly German Cohort

Superior Retinal Gene Transfer and Biodistribution Profile of Subretinal Versus Intravitreal Delivery of AAV8 in Nonhuman Primates

High Symmetry of Visual Acuity and Visual Fields in RPGR -Linked Retinitis Pigmentosa

Results from a Multicenter Trial with the New Electronic Subretinal Implant Alpha AMS in 15 Patients Blind from Inherired Retinal Dystrophies (RD)

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