SPX: Preserving End-to-End Security for Edge Computing
, 2018 Ketan Bhardwaj +4 more
openalex +2 more sources
A Computing Offloading Game for Mobile Devices and Edge Cloud Servers [PDF]
, 2018 Meiwen Li +4 more
openalex +1 more source
Assessing a Mitochondrial Disease Treatment via a Novel Statistical Technique for Accelerometer Data
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Therapeutic development for mitochondrial diseases, rare genetic disorders with pathogenic defects of oxidative phosphorylation, is hindered by unsatisfactory outcome measures. To address this problem, we provide the first clinical application of a novel, bias‐adjusted outcome measure of acceleration across a range of subjects ...
Ian W. McKeague +8 more
wiley +1 more source
Real-time monitoring and optimization methods for user-side energy management based on edge computing. [PDF]
Sci RepHuang J, Zhou S, Li G, Shen Q.
europepmc +1 more source
Orchestration Architecture for Automatic Deployment of 5G Services from Bare Metal in Mobile Edge Computing Infrastructure [PDF]
, 2018 Enrique Chirivella‐Perez +3 more
openalex +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background Managing long COVID in people with multiple sclerosis and related disorders (pwMSRD) is complex due to overlapping symptoms. To address evidence gaps, we evaluated long COVID susceptibility in pwMSRD versus controls and its associations with multi‐domain function and disability.
Chen Hu +15 more
wiley +1 more source
Enhancing healthcare AI stability with edge computing and machine learning for extubation prediction. [PDF]
Sci RepHuang KY +7 more
europepmc +1 more source
Android Unikernel: Gearing mobile code offloading towards edge computing
, 2018 Song Wu +3 more
openalex +2 more sources
An ADMM Based Method for Computation Rate Maximization in Wireless Powered Mobile-Edge Computing Networks [PDF]
, 2018 Suzhi Bi, Ying–Jun Angela Zhang
openalex +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Paroxysmal kinesigenic dyskinesia (PKD) is the most common hereditary paroxysmal movement disorder. The PRRT2 gene is the first identified causative gene and accounts for the majority of PKD. In this study, we investigated the pathogenicity of PRRT2 variants in the splice regions. Methods Patients with clinically suspected PKD and no
Jiao‐Jiao Xu +5 more
wiley +1 more source