Results 241 to 250 of about 95,882 (281)
An Integrated and Flexible Humidity Sensor for Noncontact Handwriting Recognition
A noncontact handwriting recognition system is fabricated by directly integrating a 4 × 4 flexible humidity sensing array and a designed flexible sampling circuit. Assisted with a CNN model, the handwriting recognition system can realize the recognition of handwriting digits 1–9 with an average accuracy of 98.67%.
Yu Xiao, Jingjing Yao, Shujuan Zhu
wiley +1 more source
Design, Modeling, and Control of a Soft Robotic Diaphragm‐Assist Device in a Respiratory Simulator
A soft robotic diaphragm‐assist device using fabric‐based pneumatic actuators with a 2‐step control system to optimize synchronization and support is introduced. This system can detect the initiation of breathing to trigger assistance and regulate pressures to provide the correct level of inhalation augmentation. Validation and testing are completed on
Diego Quevedo‐Moreno+5 more
wiley +1 more source
Extreme fire severity interacts with seed traits to moderate post‐fire species assemblages
Abstract Premise Climate change is globally pushing fire regimes to new extremes, with unprecedented large‐scale severe fires. Persistent soil seed banks are a key mechanism for plant species recovery after fires, but extreme fire severity may generate soil temperatures beyond thresholds seeds are adapted to.
Michi Sano+3 more
wiley +1 more source
Key challenges in diagnosing anemia in high‐altitude populations include variability in hemoglobin (Hb) concentration, associated pathological conditions, altitude‐induced plasma volume changes, and environmental factors such as contamination and nutrition.
Ayoub Boulares+11 more
wiley +1 more source
The Expanding Clinical and Genetic Spectrum of Muscle Glycogen Storage Disease 0, (GSD0B)
ABSTRACT Glycogen storage disorders are a group of genetic disorders affecting glucose homeostasis in the body. Muscular glycogen stores are essential for liberating glucose for energy supply during bursts of activity and sustained muscle work. Muscle glycogen storage disease 0 (GSD0B) is associated with biallelic variants in GYS1 causing muscular ...
Sarah Donoghue+16 more
wiley +1 more source
AP2M1 Is a Candidate Gene for Microcephaly and Intellectual Disability in 3q27.1 Deletions
ABSTRACT Deletions of the 3q26.33q27.2 region appear to correlate with a distinct phenotype, although there are few reported cases. Here, we present seven previously unreported individuals carrying de novo 3q27 deletions (under 5 Mb), which include the AP2M1 (adaptor‐related protein complex 2, mu‐1 subunit) gene and summarize data from 12 previously ...
Russell Gear+16 more
wiley +1 more source
ABSTRACT Natural History Studies can help inform clinician and caregiver expectations, form the basis of management guidelines, and provide a comparator for therapeutic intervention. In rare conditions, where collection of prospective longitudinal data is untimely and impractical, quasi‐natural history data—from multiple individuals of different ages ...
E. Woods+16 more
wiley +1 more source
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero+17 more
wiley +1 more source
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Myocardial Infarction in Respiratory Insufficiency
Archives of Internal Medicine, 1964Chronic obstructive pulmonary emphysema is common at the Veterans Administration Hospital, Coral Gables, Fla, and patients with acute myocardial infarctions are admitted with almost epidemic frequency. Yet, despite the ubiquity of both these conditions, they appeared to coexist infrequently.
Paul M. Nonkin+2 more
openaire +3 more sources