Results 301 to 310 of about 778,572 (398)

Crystallinity‐Programmed Memristive Devices Enable Reconfigurable Neuromorphic Sensing With Hardware VMM Readout

open access: yesAdvanced Electronic Materials, EarlyView.
Memristive device exhibits multi‐modal switching between volatile and nonvolatile states using a simple measurement setup. In‐sensor reservoir computing based on memristive device accurately reconstructs ECG waveforms and predicts pH changes at ultralow energy.
June Soo Kim   +7 more
wiley   +1 more source

Right ventricular dysfunctions in type 1 diabetic mice: A longitudinal study. [PDF]

open access: yesWorld J Diabetes
Yu JJ   +7 more
europepmc   +1 more source

Synthetic Electrocardiogram Spectrogram Generation Using Generative Adversarial Network‐Based Models: A Comparative Study

open access: yesAdvanced Intelligent Systems, EarlyView.
Cardiovascular diseases are leading death causes; electrocardiogram (ECG) analysis is slow, motivating machine learning and deep learning. This study compares deep convolutional generative adversarial network, conditional GAN, and Wasserstein GAN with gradient penalty (WGAN‐GP) for synthetic ECG spectrograms; Fréchet Inception Distance (FID) and ...
Giovanny Barbosa‐Casanova   +3 more
wiley   +1 more source

Plasticity of ventricle position after heart looping in heterotaxy with right isomerism. [PDF]

open access: yesSci Adv
Desgrange A   +11 more
europepmc   +1 more source

Mortality Patterns and Phenotypic Clusters in Trisomy 13: A Population‐Based Study From Japan

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Trisomy 13, the third most common autosomal trisomy after trisomy 21 and trisomy 18, is associated with a significantly high infant mortality rate. However, large‐scale studies examining causes of death in trisomy 13 remain scarce. Therefore, we aimed to better understand the mortality patterns.
Narumi Kato   +2 more
wiley   +1 more source

Identifying Pathogenic Variants in Vietnamese Children with Functional Single Ventricle Based on Whole-Exome Sequencing. [PDF]

open access: yesDiagnostics (Basel)
Tu LT   +8 more
europepmc   +1 more source

A Confirmatory Case of Severe Spondylocostal Dysostosis Caused by Biallelic Loss‐of‐Function of DMRT2

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Spondylocostal dysostosis (SCDO) is a rare genetic disorder characterized by abnormal development of the axial skeleton, resulting in malformations of the vertebrae and ribs that often impair lung development and lead to significant respiratory morbidity.
Jonathan Rips   +8 more
wiley   +1 more source

Multimodal neuroimaging of <i>Col4a1</i>-mutant mouse models of Gould syndrome. [PDF]

open access: yesFront Neurosci
Gao X   +4 more
europepmc   +1 more source

A case of arrhythmogenic right ventricular cardiomyopathy/dysplasia involving the left ventricle

open access: green, 2009
Young Keun Kim   +6 more
openalex   +1 more source

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