Results 201 to 210 of about 306,022 (339)
Artificial Intelligence for Bone: Theory, Methods, and Applications
Advances in artificial intelligence (AI) offer the potential to improve bone research. The current review explores the contributions of AI to pathological study, biomarker discovery, drug design, and clinical diagnosis and prognosis of bone diseases. We envision that AI‐driven methodologies will enable identifying novel targets for drugs discovery. The
Dongfeng Yuan +3 more
wiley +1 more source
Discrepancies in the register of primary health care visits: a 6-year time series study from Finland. [PDF]
Majuri T, Pussinen M.
europepmc +1 more source
Wearable Metamaterials with Embodied Intelligence for Programmable Control of Human Limbs Tremor
Resulting from alternating muscle contractions, tremors can severely limit human ability to perform everyday tasks like walking or talking, due to their disruptive nature. Medication and surgery may not always effectively address tremor control. A wearable device embodying programmable smart metamaterials with adaptable intelligence to meet the demand ...
Braion Barbosa de Moura +2 more
wiley +1 more source
Health inequalities among people with disabilities: an umbrella review and evidence synthesis. [PDF]
Smythe T +4 more
europepmc +1 more source
Effect Of Dentist Working Conditions On Occupational Musculoskeletal System Diseases
Selma Altındiş, Meral Soylu
openalex +2 more sources
New horizons in spine research: Intervertebral disc repair and regeneration. [PDF]
Iatridis, James C +3 more
core +2 more sources
ABSTRACT Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10‐year‐old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA).
Lauren N. Meiss +8 more
wiley +1 more source
Exploring differences in health-related benefit status in the year before, during and after specialist rehabilitation: a Norwegian case-control study. [PDF]
Skinnes MN +15 more
europepmc +1 more source
ABSTRACT Smith‐Kingsmore syndrome (SKS) is a rare autosomal dominant condition characterized by neurodevelopmental differences, macrocephaly/megalencephaly, describable facial features, sleep–wake abnormalities, hyperphagia, and overgrowth. SKS is caused by pathogenic gain‐of‐function variants in MTOR which lead to hyperactivation of the mTOR pathway ...
Carolyn R. Raski, Carlos E. Prada
wiley +1 more source

