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Pascal Escher

Showing results (11-20 of 48) with videos related to

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Investigative Ophthalmology & Visual Science|April 4, 2018
Fundus Autofluorescence Lifetime Patterns in Retinitis PigmentosaChantal Dysli, Kaspar Schuerch, Pascal Escher, et al.
Biomed Research International|March 14, 2013
IROme, a new high-throughput molecular tool for the diagnosis of inherited retinal dystrophiesDaniel F Schorderet, Alexandra Iouranova, Tatiana Favez, et al.
Advances in Experimental Medicine and Biology|March 26, 2014
IROme, a new high-throughput molecular tool for the diagnosis of inherited retinal dystrophies-a price comparison with Sanger sequencingDaniel F Schorderet, Maude Bernasconi, Leila Tiab, et al.
Ophthalmic Genetics|November 1, 2017
Variability in clinical phenotypes of PRPF8-linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactionsPascal Escher, Olga Passarin, Francis L Munier, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|November 20, 2019
Fluorescence Lifetime Patterns of Retinal Pigment Epithelium Atrophy in Patients with Stargardt Disease and Age-Related Macular DegenerationYasmin Solberg, Chantal Dysli, Pascal Escher, et al.
Retina (Philadelphia, Pa.)|April 16, 2019
RETINAL FLECKS IN STARGARDT DISEASE REVEAL CHARACTERISTIC FLUORESCENCE LIFETIME TRANSITION OVER TIMEYasmin Solberg, Chantal Dysli, Pascal Escher, et al.
Genes|December 23, 2023
Expanding Genotype/Phenotype Correlation in 2p11.2-p12 Microdeletion SyndromeAlessandra Ferrario, Nijas Aliu, Claudine Rieubland, et al.
Molecular Endocrinology (Baltimore, Md.)|October 31, 2002
A new selective peroxisome proliferator-activated receptor gamma antagonist with antiobesity and antidiabetic activityJennifer Rieusset, Fethi Touri, Liliane Michalik, et al.
Translational Vision Science & Technology|December 4, 2025
AI-Assisted Optical Coherence Tomography Segmentation for Enhanced Diagnosis of Inherited Retinal DiseasesVirginie G Peter, Michel Hayoz, Davide Scandella, et al.
Genes|June 2, 2021
Absence of Genotype/Phenotype Correlations Requires Molecular Diagnostic to Ascertain Stargardt and Stargardt-Like Swiss PatientsVirginie M M Buhler, Lieselotte Berger, André Schaller, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Investigative Ophthalmology & Visual Science|April 4, 2018
Fundus Autofluorescence Lifetime Patterns in Retinitis PigmentosaChantal Dysli, Kaspar Schuerch, Pascal Escher, et al.
Biomed Research International|March 14, 2013
IROme, a new high-throughput molecular tool for the diagnosis of inherited retinal dystrophiesDaniel F Schorderet, Alexandra Iouranova, Tatiana Favez, et al.
Advances in Experimental Medicine and Biology|March 26, 2014
IROme, a new high-throughput molecular tool for the diagnosis of inherited retinal dystrophies-a price comparison with Sanger sequencingDaniel F Schorderet, Maude Bernasconi, Leila Tiab, et al.
Ophthalmic Genetics|November 1, 2017
Variability in clinical phenotypes of PRPF8-linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactionsPascal Escher, Olga Passarin, Francis L Munier, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|November 20, 2019
Fluorescence Lifetime Patterns of Retinal Pigment Epithelium Atrophy in Patients with Stargardt Disease and Age-Related Macular DegenerationYasmin Solberg, Chantal Dysli, Pascal Escher, et al.
Retina (Philadelphia, Pa.)|April 16, 2019
RETINAL FLECKS IN STARGARDT DISEASE REVEAL CHARACTERISTIC FLUORESCENCE LIFETIME TRANSITION OVER TIMEYasmin Solberg, Chantal Dysli, Pascal Escher, et al.
Genes|December 23, 2023
Expanding Genotype/Phenotype Correlation in 2p11.2-p12 Microdeletion SyndromeAlessandra Ferrario, Nijas Aliu, Claudine Rieubland, et al.
Molecular Endocrinology (Baltimore, Md.)|October 31, 2002
A new selective peroxisome proliferator-activated receptor gamma antagonist with antiobesity and antidiabetic activityJennifer Rieusset, Fethi Touri, Liliane Michalik, et al.
Translational Vision Science & Technology|December 4, 2025
AI-Assisted Optical Coherence Tomography Segmentation for Enhanced Diagnosis of Inherited Retinal DiseasesVirginie G Peter, Michel Hayoz, Davide Scandella, et al.
Genes|June 2, 2021
Absence of Genotype/Phenotype Correlations Requires Molecular Diagnostic to Ascertain Stargardt and Stargardt-Like Swiss PatientsVirginie M M Buhler, Lieselotte Berger, André Schaller, et al.
Pageof 5