Results 41 to 50 of about 13,553 (192)

Ecofriendly Printing of Silver Nanowires with Cellulose Binder for Highly Robust Flexible Electronics

open access: yesAdvanced Electronic Materials, EarlyView.
This work reports ecofriendly silver nanowire based ink with cellulose as the binder for printed flexible electronics. After annealing, the cellulose binder provides excellent adhesion between nanowires and substrate, leading to robust electromechanical performance of the printed electronics without encapsulation.
Yuxuan Liu   +5 more
wiley   +1 more source

Novel Zwitterionic Polyurethane‐in‐Salt Electrolytes with High Ion Conductivity, Elasticity, and Adhesion for High‐Performance Solid‐State Lithium Metal Batteries

open access: yesAdvanced Energy Materials, EarlyView.
A novel zwitterionic polyurethane‐in‐salt electrolyte (zPU‐SPE) is developed, achieving high ionic conductivity (3.7 × 10⁻⁴ S cm−1 at 25 °C), superior adhesion to lithium metal, and exceptional elasticity. This innovative electrolyte enables stable solid‐state lithium metal batteries, demonstrating excellent cycling stability, strong interfacial ...
Kun Wang   +15 more
wiley   +1 more source

Liquid Metal Reversible Contacts for Flexible Tactile Sensor with High Sensitivity and Wide Detection Range

open access: yesAdvanced Intelligent Systems, EarlyView.
This work presents a novel flexible tactile sensor based on the unconventional reversible contact behavior between liquid metal droplets (LMDs), with high‐pressure sensitivity and a broad working range. The 2‐LMD‐based sensor is capable of monitoring human motion and physiological signals, while electrical impedance tomography enables precise shape and
Shuai Dong   +6 more
wiley   +1 more source

Acromegaly

open access: yesOrphanet Journal of Rare Diseases, 2008
Acromegaly is an acquired disorder related to excessive production of growth hormone (GH) and characterized by progressive somatic disfigurement (mainly involving the face and extremities) and systemic manifestations. The prevalence is estimated at 1:140,
Chanson Philippe, Salenave Sylvie
doaj   +1 more source

A New EP300‐Related Syndrome With Prominent Developmental and Immune Phenotypes

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rubinstein Taybi syndrome (RTS) is a disorder of chromatin remodeling and transcriptional regulation caused by heterozygous pathogenic variants in CREBBP and EP300. RTS is characterized by a distinct facial gestalt, intellectual disability, structural kidney and heart differences, feeding difficulties, and broad thumbs and great toes ...
Devi Priyanka Maripuri   +3 more
wiley   +1 more source

Clinical periodontal diagnosis

open access: yesPeriodontology 2000, EarlyView., 2023
Abstract Periodontal diseases include pathological conditions elicited by the presence of bacterial biofilms leading to a host response. In the diagnostic process, clinical signs such as bleeding on probing, development of periodontal pockets and gingival recessions, furcation involvement and presence of radiographic bone loss should be assessed prior ...
Giovanni E. Salvi   +5 more
wiley   +1 more source

Jacobsen syndrome

open access: yesOrphanet Journal of Rare Diseases, 2009
Jacobsen syndrome is a MCA/MR contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11. To date, over 200 cases have been reported. The prevalence has been estimated at 1/100,000 births, with a female/male ratio 2:1.
Grossfeld Paul   +2 more
doaj   +1 more source

RETALHO PERFURANTE DORSO-NASAL PARA RECONSTRUÇÃO DE DEFEITO CIRÚRGICO DO NARIZ

open access: yes, 1970
Case report: A 75-year-old female patient underwent wide excision of morpheaform basal cell carcinoma located on the alar and supra-alar right regions and lateral area of the tip of the nose.
Ermelindo Tavares   +2 more
semanticscholar   +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

Cone‐Beam Computed Tomography of Osteogenesis Imperfecta Types III and IV: Three‐Dimensional Evaluation of Craniofacial Features and Upper Airways

open access: yesJBMR Plus, 2019
This cross‐sectional study investigated the natural history of craniofacial deformities in osteogenesis imperfecta (OI) and determined the impact of three‐dimensional (3D) analysis on diagnosis and treatment planning in orthodontics and orthognathic ...
Natalie Reznikov   +5 more
doaj   +1 more source

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