Results 241 to 250 of about 1,044,595 (338)

In‐Sensor Reservoir Computing Using Ferroelectric Optoelectronic Synapse for Near‐Infrared Face Recognition

open access: yesAdvanced Intelligent Systems, EarlyView.
Near‐infrared reservoir computing system has been realized by using α‐In2Se3 optoelectronic device with concise device and algorithm architecture, achieving high accuracy near 100% and noise robustness in face recognition tasks. These findings demonstrate 2D ferroelectric device‐based optoelectronic RC system as a compact and efficient computing ...
Wenyu Songlu   +15 more
wiley   +1 more source

Interfered feature elimination coupled with feature group selection for wound infection detection by electronic nose. [PDF]

open access: yesPLoS One
Liu J   +10 more
europepmc   +1 more source

Treecreeper Drone: Adaptive Mechanism for Passive Tree Trunk Perching

open access: yesAdvanced Intelligent Systems, EarlyView.
Taking inspiration from treecreepers, a passively triggered aerial robot that can reliably perch on vertical tree trunks is presented. The friction‐based approach combines a microspine array with a tail‐like support, and then validates via dynamic analyses and flight experiments, ensuring stable performance across trunk diameters and bark textures ...
Haichuan Li   +2 more
wiley   +1 more source

Outcomes of Open Versus Closed Rhinoplasty, a Systematic Review and Meta-analysis. [PDF]

open access: yesPlast Reconstr Surg Glob Open
Abi Zeid Daou C   +3 more
europepmc   +1 more source

Standardization of Terminology, Definitions, and Outcome Criteria for Bleeding in Hereditary Hemorrhagic Telangiectasia: International Consensus Report

open access: yesAmerican Journal of Hematology, EarlyView.
ABSTRACT Hereditary hemorrhagic telangiectasia (HHT, Osler‐Weber‐Rendu disease) is the second most common inherited bleeding disorder worldwide, affecting approximately 1 in 5000 people. Development of disease‐modifying and efficacious hemostatic agents to treat HHT has finally begun after decades without such medical therapies.
Hanny Al‐Samkari   +22 more
wiley   +1 more source

Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The interstitial 6p microdeletion syndrome is characterized by dysmorphic facies and structural heart, kidney, brain, and musculoskeletal differences. RREB1 haploinsufficiency and consequent abnormal RAS‐MAPK pathway signaling have been proposed as a driver of the disease phenotype; however, apart from a single case report, the phenotype of ...
Alanna Strong   +16 more
wiley   +1 more source

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