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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

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 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 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:

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:

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

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:

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:

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

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

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

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

Testing for North Carolina Macular Dystrophy (NCMD) Variations

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

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

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

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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