MK
Publications
14
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1 - 14 of 14
Title Published in Access level OA Policy Year Views Downloads
The watchmaker's eye : Exposure keratopathy with secondary limbal stem cell deficiency due to the use of a loupeJournal français d'ophtalmologie
accessLevelRestricted
2025 22 0
Ophtalmologie : ce qui a changé en 2024Revue médicale suisse
accessLevelRestricted
2025 50 0
Infected Inclusion Cyst of a Conjunctival Nevus Treated with a Mini-Incision: A Case ReportCase reports in ophthalmology
accessLevelPublic
2024 50 118
Descemet Membrane Endothelial Keratoplasty Graft Preparation Using the Liquid Bubble Technique with Subtrabecular Hydrodissection: A Retrospective Real-Life StudyJournal of clinical medicine
accessLevelPublic
2024 41 74
Création et caractérisation fonctionnelle d’un modèle CEP amélioré de DMLA atrophique
accessLevelPublic
2024 60 76
Intradevice Repeatability and Interdevice Comparison of Two Specular Microscopy Devices in a Real-Life Setting: Tomey EM-4000 and Nidek CEM-530Medicina
accessLevelPublic
2024 59 30
Femtosecond laser-assisted cataract surgery : Update and perspectivesFrontiers in medicine
accessLevelPublic
2023 61 181
Conjunctivitis with Monkeypox Virus Positive Conjunctival SwabsOphthalmology
accessLevelPublic
2022 126 94
First Report of Flipping Endothelial Graft Technique Effectiveness in a Non-Fuchs PatientKlinische Monatsblätter für Augenheilkunde
accessLevelRestricted
2022 231 0
The SWISS IOL technique (Small-Width Incision Scleral Suture): a mini-invasive techniqueJournal of Ophthalmology
accessLevelPublic
2021 392 138
Functional and anatomical characterization of atrophic age-related macular degeneration in an aged mouse modelJournal of Ophthalmology and Research
accessLevelPublic
2021 455 312
Bilateral visual acuity loss in a 28-year-old man with Duchenne muscular dystrophyJAMA Ophthalmology
accessLevelRestricted
2021 227 6
Simultaneous intraocular and orbital involvement of NK/T-cell lymphomaJournal français d'ophtalmologie
accessLevelRestricted
2021 287 6
Taurine treatment of retinal degeneration and cardiomyopathy in a consanguineous family with SLC6A6 taurine transporter deficiencyHuman Molecular Genetics
accessLevelRestricted
2020 412 1
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