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Orphanet Journal of Rare Diseases|June 15, 2024
High prevalence of exon-13 variants in USH2A-related retinal dystrophies in Taiwanese populationYu-Wei Lin, Yu-Shu Huang, Chien-Yu Lin, et al.
NPJ Genomic Medicine|February 20, 2021
Genetic characteristics and epidemiology of inherited retinal degeneration in TaiwanTa-Ching Chen, Ding-Siang Huang, Chao-Wen Lin, et al.
Taiwan Journal of Ophthalmology|June 30, 2025
Clinical features, pathogens, and mortality of endogenous endophthalmitis: A 10-year retrospective review in Northern TaiwanYu-Hsun Chuang, Po-Jung Lai, Tzyy-Chang Ho, et al.
Nature Communications|April 26, 2024
Metabolomics facilitates differential diagnosis in common inherited retinal degenerations by exploring their profiles of serum metabolitesWei-Chieh Wang, Chu-Hsuan Huang, Hsin-Hsiang Chung, et al.
Stem Cell Research|September 8, 2022
Generation of induced pluripotent stem cells from a patient with hearing loss carrying OPA1 c.1468T>C (p.Cys490Arg) variantYen-Hui Chan, Chang-Han Ho, Cheng-Yu Tsai, et al.
Journal of Digital Imaging|July 10, 2021
Artificial Intelligence-Assisted Early Detection of Retinitis Pigmentosa - the Most Common Inherited Retinal DegenerationTa-Ching Chen, Wee Shin Lim, Victoria Y Wang, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|January 17, 2024
Injectable, Antioxidative, and Tissue-Adhesive Nanocomposite Hydrogel as a Potential Treatment for Inner Retina InjuriesYi-Chen Liu, Yi-Ke Lin, Yu-Ting Lin, et al.
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