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Human Molecular Genetics|April 23, 2021
A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defectSusanne Kohl, Pablo Llavona, Alexandra Sauer, et al.Frontiers in Bioengineering and Biotechnology|April 29, 2024
A hybrid brain-muscle-machine interface for stroke rehabilitation: Usability and functionality validation in a 2-week intensive interventionAndrea Sarasola-Sanz, Andreas M Ray, Ainhoa Insausti-Delgado, et al.Investigative Ophthalmology & Visual Science|January 28, 2004
Electroretinography as a screening method for mutations causing retinal dysfunction in miceClaudia Dalke, Jana Löster, Helmut Fuchs, et al.Biomaterials|February 16, 2017
Evaluation of polyesteramide (PEA) and polyester (PLGA) microspheres as intravitreal drug delivery systems in albino ratsTobias Peters, Seong-Woo Kim, Vinicius Castro, et al.Nature Genetics|July 14, 1998
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindnessT M Strom, G Nyakatura, E Apfelstedt-Sylla, et al.Alzheimer'S Research & Therapy|August 7, 2023
Beta to theta power ratio in EEG periodic components as a potential biomarker in mild cognitive impairment and Alzheimer's dementiaHamed Azami, Christoph Zrenner, Heather Brooks, et al.JAMA Ophthalmology|May 29, 2020
Longitudinal Microperimetric Changes of Macular Sensitivity in Stargardt Disease After 12 Months: ProgStar Report No. 13Etienne M Schönbach, Rupert W Strauss, Beatriz Muñoz, et al.Therapeutic Advances in Psychopharmacology|October 22, 2025
Biological markers of treatment response to serotonergic psychedelic therapies: a systematic reviewStanley Wong, Brett D M Jones, Mathura T Thiyagarajah, et al.Nano Letters|November 19, 2024
Solid-State Nanopores for Spatially Resolved Chemical NeuromodulationF Vacca, F Galluzzi, M Blanco-Formoso, et al.American Journal of Ophthalmology|May 19, 2020
The Effect of Attention on Fixation Stability During Dynamic Fixation Testing in Stargardt DiseaseEtienne M Schönbach, Rupert W Strauss, Mohamed A Ibrahim, et al.Pageof 78