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Articles August 2020

Cost Effectiveness of Voretigene Neparvovec for RPE65-Mediated Inherited Retinal Degeneration in Germany

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Matthias Fritz Uhrmann; Birgit Lorenz; Christian Gissel
TAGS: cost effectiveness, germany, retinal degeneration, rpe65 protein, voretigene neparvovec, quality-adjusted life years
Trans. Vis. Sci. Tech.. 2020; 9(9):17. doi: https://doi.org/10.1167/tvst.9.9.17

ARVO Annual Meeting Abstract June 2020

Patterns of photoreceptor-specific temporal contrast sensitivity losses in patients with different phenotypic variants of retinitis pigmentosa

Cord R H Huchzermeyer; Julien Fars; Birgit Lorenz; Jan J Kremers

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2336. doi:

ARVO Annual Meeting Abstract June 2020

Current management of patients with RPE65 associated inherited retinal degenerations (IRDs) in Europe. Results of a multinational survey conducted by the EVICR.net.

Birgit Lorenz; L. Ingeborgh van den Born; Joana Tavares; João Pedro Marques; Sue Lacey; Hendrik P Scholl

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3032. doi:

ARVO Annual Meeting Abstract June 2020

Current management of Inherited Retinal Degenerations (IRD) patients in Europe. Results of a multinational survey by the EVICR.net

Joana Tavares; Birgit Lorenz; L. Ingeborgh van den Born; João Pedro Marques; Sue Lacey; Hendrik P Scholl

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3040. doi:

ARVO Annual Meeting Abstract July 2019

Testing for North Carolina Macular Dystrophy (NCMD) Variations

Markus N Preising; Marc Platschek; Birgit Lorenz

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):395. doi:

ARVO Annual Meeting Abstract July 2019

Genotype-Phenotype Correlation in Inherited Retinal Diseases Caused By Biallelic CEP290 Variations

Birgit Lorenz; Ute Schneider; Hanno J Bolz; Christoph Friedburg; Monika Andrassi-Darida; Markus N Preising

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4515. doi:

ARVO Annual Meeting Abstract July 2019

Unexpected Localization of the DNA Repair Protein Ku80 within the Murine Retina.

Brigitte Muller; Franziska Wagner; Leonie Luise Laucke; Wilhelm Rheinhard; Birgit Lorenz; Knut Stieger

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4933. doi:

ARVO Annual Meeting Abstract July 2019

First steps to a genome editing approach correcting CLN3/Cln3deltaEx7/8

Tobias Wimmer; Philipp Klekamp; Maria Weller; Birgit Lorenz; Knut Stieger

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4935. doi:

ARVO Annual Meeting Abstract July 2019

DNA sequence alterations at the ISce-I target site in vivo in photoreceptors and RPE cells following AAV mediated gene transfer

Knut Stieger; Annabella Janise-Libawski; Götzmann David; Vössing Christiane; Fühler Bärbel; John Per Neidhardt; Birgit Lorenz; Brigitte Müller

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4936. doi:

Articles June 2019

Fundus-Controlled Dark Adaptometry in Young Children Without and With Spontaneously Regressed Retinopathy of Prematurity

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Wadim Bowl; Birgit Lorenz; Knut Stieger; Silke Schweinfurth; Kerstin Holve; Monika Andrassi-Darida
TAGS: child, retinopathy of prematurity, dark adaptation, rod photoreceptors
Trans. Vis. Sci. Tech.. 2019; 8(3):62. doi: https://doi.org/10.1167/tvst.8.3.62

Retina April 2019

Cone-Mediated Function Correlates to Altered Foveal Morphology in Preterm-Born Children at School Age

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Wadim Bowl; Sinan Raoof; Birgit Lorenz; Kerstin Holve; Silke Schweinfurth; Knut Stieger; Monika Andrassi-Darida
TAGS: child, language morphology, morphology, retinal cone, school (environment), perimetry, pupillometry, pupil reaction
Invest. Ophthalmol. Vis. Sci.. 2019; 60(5):1614-1620. doi: https://doi.org/10.1167/iovs.18-24892

Retina September 2018

Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+1655A>G Mutation in CEP290

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Dyon Valkenburg; Caroline van Cauwenbergh; Birgit Lorenz; Mies M. van Genderen; Mette Bertelsen; Jan-Willem R. Pott; Frauke Coppieters; Julie de Zaeytijd; Alberta A. H. J. Thiadens; Caroline C. W. Klaver; Hester Y. Kroes; Mary J. van Schooneveld; Markus Preising; Carel B. Hoyng; Bart P. Leroy; L. Ingeborgh van den Born; Rob W. J. Collin

Invest. Ophthalmol. Vis. Sci.. 2018; 59(11):4384-4391. doi: https://doi.org/10.1167/iovs.18-24817

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2018

Comparison of a handheld versus a flexible arm mounted SD-OCT for morphological evaluation of the retina in infants and toddlers

Birgit Lorenz; Kerstin Holve; Robert Knobloch; Knut Stieger; Wadim Bowl

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5202. doi:

ARVO Annual Meeting Abstract June 2017

Identification of mutations in CACNA1F in patients with incomplete CSNB applying next generation sequencing approaches

Christina Zeitz; Christelle Michiels; Marion Neuille; Christoph Friedburg; Christel Condroyer; Fiona Boyard; Aline Antonio; Markus N Preising; Vincent Meyer; Anne Boland; Jean-François Deleuze; Lilia Mesrob; Bernhard Jurklies; Birgit Lorenz; Jose Alain Sahel; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):575. doi:

ARVO Annual Meeting Abstract June 2017

A Novel Candidate Gene for Complete Achromatopsia

Markus N Preising; Anna-Maria Zuliani; Birgit Lorenz

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):2781. doi:

ARVO Annual Meeting Abstract June 2017

OPTIMIZING THE REPAIR TEMPLATE FOR HOMOLOGY DIRECTED REPAIR OF DOUBLE STRAND BREAKS

Knut Stieger; Fei Song; Birgit Lorenz

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):4471. doi:

ARVO Annual Meeting Abstract June 2017

OCT Angiography and Handheld-OCT in young children with treated or spontaneously resolved ROP

Birgit Lorenz; Kerstin Holve; Silke Schweinfurth; Robert Knobloch; Wadim Bowl

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):5553. doi:

Retinal Cell Biology April 2017

Organotypic Cultures of Adult Mouse Retina: Morphologic Changes and Gene Expression

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Brigitte Müller; Franziska Wagner; Birgit Lorenz; Knut Stieger
TAGS: adult, gene expression, mice, retina, in situ nick-end labeling, cell nucleus, photoreceptors
Invest. Ophthalmol. Vis. Sci.. 2017; 58(4):1930-1940. doi: https://doi.org/10.1167/iovs.16-20718

ARVO Annual Meeting Abstract September 2016

Investigations for the underlying genetic cause in a consanguineous family with complete achromatopsia

Markus N Preising; Anna-Maria Zuliani; Birgit Lorenz

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3167. doi:

ARVO Annual Meeting Abstract September 2016

Development of a BRET-based technique for VEGF quantification

Tobias Wimmer; Constanze Stumpf; Eva Schroeter; Birgit Lorenz; Knut Stieger

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):5052. doi:

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Cost Effectiveness of Voretigene Neparvovec for RPE65-Mediated Inherited Retinal Degeneration in Germany

Patterns of photoreceptor-specific temporal contrast sensitivity losses in patients with different phenotypic variants of retinitis pigmentosa

Current management of patients with RPE65 associated inherited retinal degenerations (IRDs) in Europe. Results of a multinational survey conducted by the EVICR.net.

Current management of Inherited Retinal Degenerations (IRD) patients in Europe. Results of a multinational survey by the EVICR.net

Testing for North Carolina Macular Dystrophy (NCMD) Variations

Genotype-Phenotype Correlation in Inherited Retinal Diseases Caused By Biallelic CEP290 Variations

Unexpected Localization of the DNA Repair Protein Ku80 within the Murine Retina.

First steps to a genome editing approach correcting CLN3/Cln3deltaEx7/8

DNA sequence alterations at the ISce-I target site in vivo in photoreceptors and RPE cells following AAV mediated gene transfer

Fundus-Controlled Dark Adaptometry in Young Children Without and With Spontaneously Regressed Retinopathy of Prematurity

Cone-Mediated Function Correlates to Altered Foveal Morphology in Preterm-Born Children at School Age

Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+1655A>G Mutation in CEP290

Comparison of a handheld versus a flexible arm mounted SD-OCT for morphological evaluation of the retina in infants and toddlers

Identification of mutations in CACNA1F in patients with incomplete CSNB applying next generation sequencing approaches

A Novel Candidate Gene for Complete Achromatopsia

OPTIMIZING THE REPAIR TEMPLATE FOR HOMOLOGY DIRECTED REPAIR OF DOUBLE STRAND BREAKS

OCT Angiography and Handheld-OCT in young children with treated or spontaneously resolved ROP

Organotypic Cultures of Adult Mouse Retina: Morphologic Changes and Gene Expression

Investigations for the underlying genetic cause in a consanguineous family with complete achromatopsia

Development of a BRET-based technique for VEGF quantification

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