Design and evaluation of high-speed train head shape based on data-driven analysis. [PDF]
Hu Q, Wu X, Lei A, Bian L.
europepmc +1 more source
Joint optimization of high-speed train timetables, speed levels and stop plans for increasing capacity based on a compressed multilayer space-time network. [PDF]
Chen A, Zhang X, Chen J, Wang Z.
europepmc +1 more source
Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina +11 more
wiley +1 more source
A Diffusion-Based Data Augmentation Framework for Few-Shot Fault Diagnosis of Intelligent High-Speed Train Components. [PDF]
Xu J +6 more
europepmc +1 more source
A Hybrid SVD-Based Denoising and Self-Adaptive TMSST for High-Speed Train Axle Bearing Fault Detection. [PDF]
Deng F, Liu C, Liu Y, Hao R.
europepmc +1 more source
M. Ahmed Ali Baig +2 more
openaire +1 more source
ABSTRACT Background Emerging evidence suggests that low‐frequency neural oscillations are dynamically regulated by consciousness levels, with the recovery of low cortical activity potentially serving as a neurophysiological substrate for conscious emergence. Targeted enhancement of these low‐frequency rhythms in patients with disorders of consciousness
Chuan Xu +10 more
wiley +1 more source
Reliability Assessment of High-Speed Train Gearbox Based on Digital Twin and WHO-WPHM. [PDF]
Wang T +6 more
europepmc +1 more source
Geovisualizing cancelled air and high-speed train services during the outbreak of COVID-19 in China. [PDF]
Wang J, Du D, Ma L.
europepmc +1 more source
Epilepsy‐Associated Variants of a Single SCN1A Codon Exhibit Divergent Functional Properties
ABSTRACT Objective Pathogenic variants in SCN1A, which encodes the voltage‐gated sodium channel NaV1.1, are associated with multiple epilepsy syndromes exhibiting a range of clinical severity. SCN1A variants are reported in different syndromes, including Dravet syndrome, which is associated with loss‐of‐function, whereas neonatal/infantile‐onset ...
Lanie N. Liebovitz +3 more
wiley +1 more source

