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ARVO Annual Meeting Abstract June 2022

Characterizing the refractive error during the first 2 decades of life in patients with congenital stationary night blindness

Austin David Igelman; Thomas Khuu; Alaa Tayyib; Milda Reith; Birgit Lorenz; Erin O'Neil; Shaden Yassin; Andrew Stephenson; Emily Krauss; Ogul Uner; Justin Grassmeyer; Paul Yang; Lorri Wilson; Douglas Fredrick; Mark E Pennesi

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):253 – A0107. doi:

ARVO Annual Meeting Abstract June 2022

Current management of patients with RPE65 mutation-associated Inherited Retinal Degenerations ( RPE65 -IRD) in Europe. Results of a 2-year follow-up multinational survey by the European Vision Institute Clinical Research Network (EVICR.net) and the European Reference Network for Rare Eye Diseases (ERN-EYE)

Birgit Lorenz; Joana Tavares; Ingeborgh van den Born; João Pedro Marques; Katarina Stingl; Elisabetta Pilotto; Peter Charbel Issa; Dorothee Leroux; Helene Dollfus; Hendrik P Scholl

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):4488 – F0275. doi:

ARVO Annual Meeting Abstract June 2022

Current management of Inherited Retinal Degenerations (IRD) patients in Europe. Results of a 2 years follow-up multinational survey by EVICR.net and ERN-EYE

Joana Tavares; Birgit Lorenz; Ingeborgh van den Born; João Pedro Marques; Katarina Stingl; Elisabetta Pilotto; Peter Charbel Issa; Dorothee Leroux; Helene Dollfus; Hendrik P Scholl

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):4481 – F0268. doi:

ARVO Annual Meeting Abstract June 2022

Multimodal widefield imaging for postoperative monitoring in patients treated with voretigene neparvovec

Philipp Herrmann; Birgit Lorenz; Johanna Pauline Scholz; Ralf Brinken; Markus N Preising; Kristina Küpper; Naike Cavriani; Laura Wirtz; Frank G Holz

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):4400 – F0079. doi:

ARVO Annual Meeting Abstract June 2022

Re-treatments after laser coagulation or anti-VEGF injections in infants treated for retinopathy of prematurity – data from the German ROP registry

Johanna Madeleine Pfeil; Teresa Barth; Wolf Lagrèze; Birgit Lorenz; Karsten Hufendiek; Raffael Liegl; Helge Breuss; Sebastian Bemme; Jakob Ferdinand Meyer; Barbara Glitz; Daniela Suesskind; Ameli Gabel-Pfisterer; Christos Skevas; Tim U Krohne; Vinodh Kakkassery; Andreas Stahl

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):4198 – F0258. doi:

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

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

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:

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Characterizing the refractive error during the first 2 decades of life in patients with congenital stationary night blindness

Current management of Inherited Retinal Degenerations (IRD) patients in Europe. Results of a 2 years follow-up multinational survey by EVICR.net and ERN-EYE

Multimodal widefield imaging for postoperative monitoring in patients treated with voretigene neparvovec

Re-treatments after laser coagulation or anti-VEGF injections in infants treated for retinopathy of prematurity – data from the German ROP registry

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

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

A Novel Candidate Gene for Complete Achromatopsia

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

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