Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Yl Cheung"'
Autor:
Jeffrey Peacock, David Provenzano, Michael Fishman, Kasra Amirdelfan, Todd Bromberg, Todd Schmidt, Thomas White, Prabhdeep Grewal, Rafael Justiz, Aaron Calodney, Amr El-Naggar, Binit Shah, Michael Esposito, Kliment Gatzinsky, Jan Willem Kallewaard, Charles Cain, Andrew Cleland, Aaron YL. Cheung, Erin Theis
Publikováno v:
Neuromodulation: Technology at the Neural Interface. 25:S15
Autor:
John Hatheway, Michael Danko, Chris Beuer, Michael Saulino, Katherine Stromberg, Garrett Grenier, Aaron YL. Cheung, Robert Spencer
Publikováno v:
Neuromodulation: Technology at the Neural Interface. 25:S9
Autor:
Michael Fishman, Harold Cordner, Rafael Justiz, David Provenzano, Binit Shah, Christopher Merrell, Julian Naranjo, Philip Kim, Aaron Calodney, Richard Bundschu, Mahendra Sanapati, Vipul Mangal, David Cedeno, Aaron YL. Cheung, Ricardo Vallejo
Publikováno v:
Neuromodulation: Technology at the Neural Interface. 25:S4
Autor:
Michael Fishman, Harold Cordner, Rafael Justiz, David Provenzano, Binit Shah, Christopher Merrell, Julian Naranjo, Philip Kim, Aaron Calodney, Richard Bundschu, Mahendra Sanapati, Vipul Mangal, David Cedeno, Aaron YL. Cheung, Ricardo Vallejo
Publikováno v:
Neuromodulation: Technology at the Neural Interface. 25:S2
Publikováno v:
Neuromodulation: Technology at the Neural Interface. 25:S3
Publikováno v:
Neuromodulation: Technology at the Neural Interface. 25:S3
Autor:
Ya Xing Wang, Tien Y Wong, Charumathi Sabanayagam, Daniel S W Ting, E. Shyong Tai, Ching-Yu Cheng, Dejiang Xu, Carol Yl Cheung, Simon Nusinovici, Cynthia C. Lim, Haslina Hamzah, Riswana Banu, Mong Li Lee, Jost B. Jonas, Wynne Hsu, Yih Chung Tham
Publikováno v:
The Lancet. Digital health. 2(6)
Summary Background Screening for chronic kidney disease is a challenge in community and primary care settings, even in high-income countries. We developed an artificial intelligence deep learning algorithm (DLA) to detect chronic kidney disease from
Publikováno v:
Frontiers in Psychiatry, Vol 3 (2012)
Rett Syndrome (RTT) is a neurodevelopmental disorder that affects girls due primarily to heterozygous mutations in the X-linked gene encoding methyl-CpG binding protein 2 (MECP2). Random X-chromosome inactivation (XCI) results in cellular mosaicism i
Externí odkaz:
https://doaj.org/article/606b725663cd42b3843e4facbab1bc27
Publikováno v:
Hong Kong Journal of Radiology. :221-226
Publikováno v:
Hong Kong Journal of Radiology. 17:281-284