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Tsioti, Ioanna; Steiner, Beatrice L; Escher, Pascal; Zinkernagel, Martin S; Benz, Peter M; Kokona, Despina (2024). Systemic Lipopolysaccharide Exposure Exacerbates Choroidal Neovascularization in Mice. Ocular immunology and inflammation, 32(1), pp. 19-30. Taylor & Francis 10.1080/09273948.2022.2147547
Ferrario, Alessandra; Aliu, Nijas; Rieubland, Claudine; Vuilleumier, Sébastian; Grabe, Hilary M.; Escher, Pascal (2023). Expanding Genotype/Phenotype Correlation in 2p11.2-p12 Microdeletion Syndrome. Genes, 14(12) MDPI, Molecular Diversity Preservation International 10.3390/genes14122222
Reche, Jelena; Stocker, Andrea B; Henchoz, Virgilia; Habra, Oussama; Escher, Pascal; Wolf, Sebastian; Zinkernagel, Martin S (2023). High-Resolution Optical Coherence Tomography in Healthy Individuals Provides Resolution at the Cellular and Subcellular Levels. Translational vision science & technology, 12(7), p. 12. Association for Research in Vision and Ophthalmology 10.1167/tvst.12.7.12
Hundsberger, Felix; Escher, Pascal; Schaller, André; Valmaggia, Christophe; Todorova, Margarita G (2023). The Value of a Combined Ophthalmogenetic Approach in Differentiating a Presumed Case of Isolated Retinitis Pigmentosa from Refsum Disease. Klinische Monatsblätter für Augenheilkunde, 240(4), pp. 549-552. Thieme 10.1055/a-2055-1051
Yahya, Faady; Escher, Pascal; Rivolta, Carlo; Scholl, Hendrik Pn; Roulez, Francoise (2023). SPATA7-Associated Juvenile Retinitis Pigmentosa in Two Brothers from a Consanguineous Iraqi Family in Switzerland. Klinische Monatsblätter für Augenheilkunde, 240(4), pp. 544-548. Thieme 10.1055/a-2009-0498
Sanlialp, Ayse; Escher, Pascal; Schaller, André; Todorova, Margarita (2023). Clinical Heterogeneity in Two Siblings Harbouring a Heterozygous PRPH2 Pathogenic Variant. Klinische Monatsblätter für Augenheilkunde, 240(4), pp. 536-543. Thieme 10.1055/a-2034-6250
Tsioti, Ioanna; Steiner, Beatrice L; Escher, Pascal; Zinkernagel, Martin S; Benz, Peter M; Kokona, Despina (2023). Endothelial Toll-like receptor 4 is required for microglia activation in the murine retina after systemic lipopolysaccharide exposure. Journal of neuroinflammation, 20(1), p. 25. BioMed Central 10.1186/s12974-023-02712-1
Escher, Pascal; Schuerch, Kaspar; Zinkernagel, Martin S.; Tran, Viet Hoai; Munier, Francis Louis (2022). Enhanced S-cone syndrome and NR2E3-associated disorders. In: Black, Graeme C. M.; Ashworth, Jane L.; Sergouniotis, Panagiotis I. (eds.) Clinical Ophthalmic Genetics and Genomics (pp. 176-180). Elsevier
Janeschitz-Kriegl, Lucas; Kamdar, Dhryata; Quinodoz, Mathieu; Kaminska, Karolina; Folcher, Marc; György, Bence; Meyer, Peter; Wild, Andreas; Escher, Pascal; Scholl, Hendrik P N; Rivolta, Carlo; Goldblum, David (2022). c.-61G>A in OVOL2 is a Pathogenic 5' Untranslated Region Variant Causing Posterior Polymorphous Corneal Dystrophy 1. Cornea, 41(1), pp. 89-94. Wolters Kluwer Health 10.1097/ICO.0000000000002843
Venturini, Giulia; Kokona, Despina; Steiner, Beatrice L; Bulla, Emanuele G; Jovanovic, Joel; Zinkernagel, Martin S; Escher, Pascal (2021). Author Correction: In vivo analysis of onset and progression of retinal degeneration in the Nr2e3rd7/rd7 mouse model of enhanced S-cone sensitivity syndrome. Scientific reports, 11(1), p. 20668. Springer Nature 10.1038/s41598-021-00207-8
Venturini, Giulia; Kokona, Despina; Steiner, Beatrice L; Bulla, Emanuele G; Jovanovic, Joel; Zinkernagel, Martin S; Escher, Pascal (2021). In vivo analysis of onset and progression of retinal degeneration in the Nr2e3rd7/rd7 mouse model of enhanced S-cone sensitivity syndrome. Scientific reports, 11(1), p. 19032. Springer Nature 10.1038/s41598-021-98271-7
Buhler, Virginie M. M.; Berger, Lieselotte; Schaller, André; Zinkernagel, Martin S.; Wolf, Sebastian; Escher, Pascal (2021). Absence of Genotype/Phenotype Correlations Requires Molecular Diagnostic to Ascertain Stargardt and Stargardt-Like Swiss Patients. Genes, 12(6) MDPI, Molecular Diversity Preservation International 10.3390/genes12060812
Chatzistergiou, Vasileia; Papasavvas, Ioannis; Escher, Pascal; Durig, Jacques; Vaudaux, Jean; Pournaras, Jean-Antoine; Ambresin, Aude (2020). Optical Coherence Tomography Analysis of Cystoid Macular Edema in Retinal Dystrophy Treated with Oral Acetazolamide: Two Cases. Klinische Monatsblätter für Augenheilkunde, 237(4), pp. 484-486. Thieme 10.1055/a-1068-2762
Vaclavik, Veronika; Naderi, Francine; Schaller, André; Escher, Pascal (2020). Longitudinal case study and phenotypic multimodal characterization of McArdle disease-linked retinopathy: insight into pathomechanisms. Ophthalmic genetics, 41(1), pp. 73-78. Taylor & Francis 10.1080/13816810.2020.1727536
Solberg, Yasmin; Dysli, Chantal; Escher, Pascal; Berger, Lisa; Wolf, Sebastian; Zinkernagel, Martin S. (2020). Fluorescence Lifetime Patterns of Retinal Pigment Epithelium Atrophy in Patients with Stargardt Disease and Age-Related Macular Degeneration. Ophthalmologica, 243(3), pp. 195-206. Karger 10.1159/000503567
Escher, Pascal (2019). Comment: Novel mutations in the OPN1LW and NR2R3 genes in a patient with blue cone monochromacy. Ophthalmic genetics, 40(6), p. 591. Taylor & Francis 10.1080/13816810.2019.1573908
Solberg, Yasmin; Dysli, Chantal; Escher, Pascal; Berger, Lisa; Wolf, Sebastian; Zinkernagel, Martin (2019). RETINAL FLECKS IN STARGARDT DISEASE REVEAL CHARACTERISTIC FLUORESCENCE LIFETIME TRANSITION OVER TIME. Retina, 39(5), pp. 879-888. Wolters Kluwer 10.1097/IAE.0000000000002519
Kokona, Despina; Ebneter, Andreas; Escher, Pascal; Zinkernagel, Martin S. (2018). Colony-stimulating factor 1 receptor inhibition prevents disruption of the blood-retina barrier during chronic inflammation. Journal of neuroinflammation, 15(1), p. 340. BioMed Central 10.1186/s12974-018-1373-4
Dysli, Chantal-Simone; Schürch, Kaspar Werner; Escher, Pascal; Wolf, Sebastian; Zinkernagel, Martin (2018). Fundus Autofluorescence Lifetime Patterns in Retinitis Pigmentosa. Investigative ophthalmology & visual science, 59(5), pp. 1769-1778. Association for Research in Vision and Ophthalmology 10.1167/iovs.17-23336
Escher, Pascal; Passarin, Olga; Munier, Francis L; Tran, Viet H; Vaclavik, Veronika (2018). Variability in clinical phenotypes of PRPF8-linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions. Ophthalmic genetics, 39(1), pp. 80-86. Taylor & Francis 10.1080/13816810.2017.1393825
Olivares, Ana Maria; Han, Yinan; Soto, David; Flattery, Kyle; Marini, Joseph; Mollema, Nissa; Haider, Ali; Escher, Pascal; DeAngelis, Margaret M; Haider, Neena B (2017). The nuclear hormone receptor gene Nr2c1 (Tr2) is a critical regulator of early retina cell patterning. Developmental biology, 429(1), pp. 343-355. Elsevier 10.1016/j.ydbio.2017.05.021
Olivares, Ana Maria; Han, Yinan; Soto, David; Flattery, Kyle; Marini, Joseph; Molemma, Nissa; Haider, Ali; Escher, Pascal; DeAngelis, Margaret M; Haider, Neena B (2017). Corrigendum to "The Nuclear Hormone Receptor Nr2c1 (Tr2) is a critical regulator of early retina cell pattering" [Dev. Biol. 16 (2017) 30797-7]. Developmental biology, 429(1), p. 370. Elsevier 10.1016/j.ydbio.2017.07.009
