Publikationen (177) Publikationen, an denen Forscher/innen teilgenommen haben

2024

  1. A 6-Month Follow-Up Comparative Study of Single-Step Transepithelial Photorefractive Keratectomy (Trans-PRK) Using the StreamLight Software with and without Epithelial Thickness Customization

    Clinical Ophthalmology, Vol. 18, pp. 2831-2841

  2. Características del desprendimiento de retina pseudofáquico y factores de riesgo de recidiva

    Archivos de la Sociedad Española de Oftalmologia, Vol. 99, Núm. 9, pp. 365-372

  3. Comparison between a new transepithelial PRK vs. conventional alcohol-assisted PRK: Corneal densitometry and aberrometry study

    European Journal of Ophthalmology

  4. Müller glial cells located in the peripheral retina are more susceptible to high pressure: implications for glaucoma

    Cell and Bioscience, Vol. 14, Núm. 1

  5. Next-generation sequencing to genetically diagnose a diverse range of inherited eye disorders in 15 consanguineous families from Pakistan

    Experimental Eye Research, Vol. 244

  6. PRPH2-Related Retinal Dystrophies: Mutational Spectrum in 103 Families from a Spanish Cohort

    International Journal of Molecular Sciences, Vol. 25, Núm. 5

  7. Validación Rasch del Keratoconus End-Points Assessment Questionnaire en población española con queratocono

    Archivos de la Sociedad Española de Oftalmologia, Vol. 99, Núm. 8, pp. 323-330

  8. Validation of a rapid collagenase activity detection technique based on fluorescent quenched gelatin with synovial fluid samples

    BMC Biotechnology, Vol. 24, Núm. 1

  9. Visual and patient reported outcomes provided by a refractive multifocal intraocular lens based on continuous transitional focus

    Eye and Vision, Vol. 11, Núm. 1

  10. Visual, Refractive, Functional, and Patient Satisfaction Outcomes After Implantation of a New Trifocal Diffractive Intraocular Lens

    Clinical Ophthalmology, Vol. 18, pp. 2785-2795

  11. Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients

    Human Genetics and Genomics Advances, Vol. 5, Núm. 3

2023

  1. A Pilot Study of a Panel of Ocular Inflammation Biomarkers in Patients with Primary Sjögren’s Syndrome

    Current Issues in Molecular Biology, Vol. 45, Núm. 4, pp. 2881-2894

  2. ABCA4 c.6480-35A>G, a novel branchpoint variant associated with Stargardt disease

    Frontiers in Genetics, Vol. 14

  3. Are all primary retinal detachments the same? Anatomic and functional differences between phakic and pseudophakic patients

    International Journal of Retina and Vitreous, Vol. 9, Núm. 1

  4. Combined Single Gene Testing and Genome Sequencing as an Effective Diagnostic Approach for Anophthalmia and Microphthalmia Patients

    Genes, Vol. 14, Núm. 8

  5. PRPF8 increases the aggressiveness of hepatocellular carcinoma by regulating FAK/AKT pathway via fibronectin 1 splicing

    Experimental and Molecular Medicine, Vol. 55, Núm. 1, pp. 132-142

  6. Predictive Factors and Management of Macular Edema after Retropupillary Iris-Claw Intraocular Lens Implantation in Aphakia: National Multicenter Audit—Report 2

    Journal of Clinical Medicine, Vol. 12, Núm. 2

  7. Shedding light on the viscoelastic behavior of artificial and human tears: A microrheological approach

    Physics of Fluids, Vol. 35, Núm. 7

  8. The role of Eudragit® as a component of hydrogel formulations for medical devices

    Journal of Materials Chemistry B, Vol. 11, Núm. 38, pp. 9276-9289

2022

  1. Assessing the Utility and Patient Satisfaction of Virtual Retina Clinics During COVID-19 Pandemic

    Clinical Ophthalmology, Vol. 16, pp. 311-321