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ARVO Annual Meeting Abstract June 2024

AI-Enhanced OCT Image Analysis for Inherited Retinal Diseases

Virginie Peter; Hayoz Michel; Davide Scandella; Raphael Sznitman; Martin Sebastian Zinkernagel; Pascal Escher

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):3761.

ARVO Annual Meeting Abstract June 2024

A proteomic approach to investigate the complement system in the retinal pigment epithelium (RPE) during systemic inflammation

Vittoria Spero; Volker Enzmann; Sophie Braga-Lagache; Pascal Escher; Martin Sebastian Zinkernagel

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):3177.

ARVO Annual Meeting Abstract June 2024

PRPH2 Gene Mutations and Associated Phenotypes in IRD patients with diverse genetic background.

Christopher Hallock; Riccardo Sangermano; Elfride De Baere; Siying Lin; Jennifer Thompson; Pascal Escher; Andrea L Vincent; Kaylie D Webb-Jones; Monika Grudzinska Pechhacker; Jacque L Duncan; Samer Khateb; Tamar Ben-Yosef; David G Birch; Andrew Webster; Radha Ayyagari

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):5297.

Vision Sciences Society Annual Meeting Abstract August 2023

The impact of cerebral visual impairment on school related competences in elementary school children

Sara Monteiro; Géraldine Hipp; Pascale Esch; Sonja Ugen

Journal of Vision. 2023; 23(9):4889. https://doi.org/10.1167/jov.23.9.4889

Retina July 2023

High-Resolution Optical Coherence Tomography in Healthy Individuals Provides Resolution at the Cellular and Subcellular Levels

PDF

Jelena Reche; Andrea B. Stocker; Virgilia Henchoz; Oussama Habra; Pascal Escher; Sebastian Wolf; Martin S. Zinkernagel
TAGS: cell nucleus, fiberoptic examinations anoscopy high resolution, optical coherence tomography, retina
Trans. Vis. Sci. Tech.. 2023; 12(7):12. https://doi.org/10.1167/tvst.12.7.12

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2023

Detection of outer retinal changes during diurnal rhythm and light adaptation by high resolution optical coherence tomography

Jelena Reche; Andrea B. Stocker; Virgilia Henchoz; Sebastian Wolf; Pascal Escher; Martin Sebastian Zinkernagel

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):3348.

ARVO Annual Meeting Abstract June 2023

Impaired corepressor binding is a disease mechanism in enhanced S-cone syndrome (ESCS)

Pascal Escher; Jelena Murar; Emanuele Bulla; Beatrice Steiner

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):5089.

ARVO Annual Meeting Abstract July 2019

Posterior Pole Involvement in Patients affected by Dystrophia Myotonica 1 (DM1): Correlation to Genotype?

Karen Schaal; Mathias Abegg; Kaspar Schuerch; Claudine Rieubland; Muriel Ott; Lilly Khamsy; Urs Graf; Fatma Kivrak Pfiffner; Wolfgang Berger; Andre Schaller; Pascal Escher

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1590.

ARVO Annual Meeting Abstract July 2019

Molecular and cellular mechanisms in Nr2e3 -linked retinal degenerations

Pascal Escher; Emanuele Bulla; Beatrice Steiner; Despina Kokona; Martin Sebastian Zinkernagel; Giulia Venturini

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4898.

Clinical Trials April 2018

Fundus Autofluorescence Lifetime Patterns in Retinitis Pigmentosa

PDF

Chantal Dysli; Kaspar Schuerch; Pascal Escher; Sebastian Wolf; Martin S. Zinkernagel
TAGS: diagnostic imaging, fluorescence, fundus autofluorescence imaging, retinitis pigmentosa
Invest. Ophthalmol. Vis. Sci.. 2018; 59(5):1769-1778. https://doi.org/10.1167/iovs.17-23336

Letters to the Editor April 2016

Presence of a Triple Concentric Autofluorescence Ring in NR2E3 -p.G56R–Linked Autosomal Dominant Retinitis Pigmentosa (ADRP)

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Pascal Escher; Veronika Vaclavik; Francis L. Munier; H. Viet Tran
TAGS: autofluorescence, retinitis pigmentosa
Invest. Ophthalmol. Vis. Sci.. 2016; 57(4):2001-2002. https://doi.org/10.1167/iovs.16-19459

ARVO Annual Meeting Abstract June 2015

The nuclear hormone receptor gene Nr2c1 ( Tr2 ) is a Critical Regulator of Cone Photoreceptor Cell Patterning

Ana Maria Olivares; Yinan Han; David Soto; Kyle Flattery; Joe Marini; Pascal Escher; Margaret M DeAngelis; Neena B Haider

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4639.

ARVO Annual Meeting Abstract April 2014

Nuclear Hormone Receptors are Potent Genetic Modifiers that Rescue Multiple Models of Retinal Degeneration

Neena B Haider; Ana B Olivares; Nelly M Cruz; Pascal Escher; Margaret M DeAngelis

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):2182.

ARVO Annual Meeting Abstract June 2013

Identification of a novel genetic model for retinal neovascularization

Mariacarmela Allocca; Barrett Leehy; Joseph White; Leo Kim; Magali Saint-Geniez; Pascal Escher; Dean Eliott; Eric Pierce; Margaret DeAngelis; Neena Haider

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):264.

Retina July 2012

Double Concentric Autofluorescence Ring in NR2E3 -p.G56R-Linked Autosomal Dominant Retinitis Pigmentosa

PDF

Pascal Escher; Hoai V. Tran; Veronika Vaclavik; Francois X. Borruat; Daniel F. Schorderet; Francis L. Munier
TAGS: autofluorescence, family, retinitis pigmentosa, eye, pigment
Invest. Ophthalmol. Vis. Sci.. 2012; 53(8):4754-4764. https://doi.org/10.1167/iovs.11-8693

Retinal Cell Biology July 2011

Altered Expression of the Transcription Factor Mef2c during Retinal Degeneration in Rpe65 –/– Mice

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Pascal Escher; Daniel F. Schorderet; Sandra Cottet
TAGS: mice, retinal degeneration, transcription factor, retina, proteins, rna, messenger, genes, transcription, genetic
Invest. Ophthalmol. Vis. Sci.. 2011; 52(8):5933-5940. https://doi.org/10.1167/iovs.10-6978

ARVO Annual Meeting Abstract April 2011

Autofluorescence Study In NR2E3 p.G56R-linked Autosomal Dominant Retinitis Pigmentosa In A Single Kindred

Hoai V. Tran; Pascal Escher; Veronika Vaclavik; Isabelle Favre; Hasret Bajrami; Francois X. Borruat; Daniel F. Schorderet; Francis L. Munier

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):6604.

Retina September 2010

The PROM1 Mutation p.R373C Causes an Autosomal Dominant Bull's Eye Maculopathy Associated with Rod, Rod–Cone, and Macular Dystrophy

PDF

Michel Michaelides; Marie-Claire Gaillard; Pascal Escher; Leila Tiab; Matthew Bedell; François-Xavier Borruat; Daniel Barthelmes; Ruben Carmona; Kang Zhang; Edward White; Michelle McClements; Anthony G. Robson; Graham E. Holder; Keith Bradshaw; David M. Hunt; Andrew R. Webster; Anthony T. Moore; Daniel F. Schorderet; Francis L. Munier
TAGS: eye, family, macular disorders, macular dystrophy, mutation, retinal cone, rod photoreceptors, atrophy, phenotype
Invest. Ophthalmol. Vis. Sci.. 2010; 51(9):4771-4780. https://doi.org/10.1167/iovs.09-4561

Articles November 1994

Periodic alternating nystagmus in humans with albinism.

PDF

R V Abadi; E Pascal
TAGS: albinism, nystagmus, periodic alternating
Invest. Ophthalmol. Vis. Sci.. 1994; 35(12):4080-4086.

Articles April 1993

Incremental light detection thresholds across the central visual field of human albinos.

PDF

R V Abadi; E Pascal
TAGS: visual fields
Invest. Ophthalmol. Vis. Sci.. 1993; 34(5):1683-1690.

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AI-Enhanced OCT Image Analysis for Inherited Retinal Diseases

A proteomic approach to investigate the complement system in the retinal pigment epithelium (RPE) during systemic inflammation

PRPH2 Gene Mutations and Associated Phenotypes in IRD patients with diverse genetic background.

The impact of cerebral visual impairment on school related competences in elementary school children

High-Resolution Optical Coherence Tomography in Healthy Individuals Provides Resolution at the Cellular and Subcellular Levels

Detection of outer retinal changes during diurnal rhythm and light adaptation by high resolution optical coherence tomography

Impaired corepressor binding is a disease mechanism in enhanced S-cone syndrome (ESCS)

Posterior Pole Involvement in Patients affected by Dystrophia Myotonica 1 (DM1): Correlation to Genotype?

Molecular and cellular mechanisms in Nr2e3 -linked retinal degenerations

Fundus Autofluorescence Lifetime Patterns in Retinitis Pigmentosa

Presence of a Triple Concentric Autofluorescence Ring in NR2E3 -p.G56R–Linked Autosomal Dominant Retinitis Pigmentosa (ADRP)

The nuclear hormone receptor gene Nr2c1 ( Tr2 ) is a Critical Regulator of Cone Photoreceptor Cell Patterning

Nuclear Hormone Receptors are Potent Genetic Modifiers that Rescue Multiple Models of Retinal Degeneration

Identification of a novel genetic model for retinal neovascularization

Double Concentric Autofluorescence Ring in NR2E3 -p.G56R-Linked Autosomal Dominant Retinitis Pigmentosa

Altered Expression of the Transcription Factor Mef2c during Retinal Degeneration in Rpe65 –/– Mice

Autofluorescence Study In NR2E3 p.G56R-linked Autosomal Dominant Retinitis Pigmentosa In A Single Kindred

The PROM1 Mutation p.R373C Causes an Autosomal Dominant Bull's Eye Maculopathy Associated with Rod, Rod–Cone, and Macular Dystrophy

Periodic alternating nystagmus in humans with albinism.

Incremental light detection thresholds across the central visual field of human albinos.

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