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Orphanet Journal of Rare Diseases|September 20, 2024
A rare transcript homozygous variants in CLRN1(USH3A) causes Usher syndrome type 3 in a Chinese familySuyang Wang, Chen Yang Xu, Yiming Zhu, et al.
Analytical Methods : Advancing Methods and Applications|August 8, 2023
Regulated synthesis of an Au NB-DT@Ag bimetallic core-molecule-shell nanostructure for reliable SERS detectionHaiting Ren, Yan Sun, Junjie Wang, et al.
The Journal of Clinical Endocrinology and Metabolism|November 26, 2014
Association of vitamin D status of septic patients in intensive care units with altered procalcitonin levels and mortalityZhaoyan Chen, Zuojie Luo, Xiaoqin Zhao, et al.
European Heart Journal. Digital Health|November 21, 2025
A deep learning-based pipeline for large-scale echocardiography data curation and measurementsJieyu Hu, Sindre Hellum Olaisen, David Pasdeloup, et al.
European Heart Journal. Cardiovascular Imaging|October 26, 2023
Automatic measurements of left ventricular volumes and ejection fraction by artificial intelligence: clinical validation in real time and large databasesSindre Olaisen, Erik Smistad, Torvald Espeland, et al.
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