Exploring Patient Heterogeneity in Service Quality Gaps and Satisfaction: Insights from Outpatient Care. [PDF]
Inchiyil VS, Syed AF.
europepmc +1 more source
Sex Representation in US Stroke Clinical Trials: A Decade of Trends and Challenges
ABSTRACT Objective Stroke remains a major cause of disability and mortality in the US, with significant sex‐based disparities, and females remain underrepresented in stroke clinical trials. We aimed to examine sex representation in US‐based stroke clinical trials, identify trial characteristics associated with higher female enrollment (≥ 50%), and ...
Chaitali Dagli +5 more
wiley +1 more source
Sensitivity characteristics of the Hirota-Maccari system in nonlinear materials. [PDF]
Khater MMA, Alfalqi SH, Vokhmintsev A.
europepmc +1 more source
ABSTRACT Objective This analysis evaluates the effect of successful reperfusion on functional outcomes after MT, stratified by admission National Institutes of Health Stroke Scale (NIHSS) and Alberta Stroke Program Early CT Score (ASPECTS) as surrogates for clinical‐core mismatch, using multicenter registry data.
Felix Schlicht +53 more
wiley +1 more source
Dall-E in hand surgery: Exploring the utility of ChatGPT image generation: Correspondence. [PDF]
Daungsupawong H, Wiwanitkit V.
europepmc +1 more source
Clinical Validation of Plasma p‐217tau in Neurological Diseases
ABSTRACT Objective Plasma p‐217tau is a minimally invasive but specific biomarker for diagnosing Alzheimer's disease (AD). However, its disease specificity remains to be clinically evaluated. We validated the reliability of the p‐217tau biomarker in 12 other neurological diseases.
Takeshi Kawarabayashi +13 more
wiley +1 more source
The ATHENE Project: The importance of bricolage in personalising assisted living technologies
Rob Procter +5 more
doaj
Nurses' experiences with inhospital continuous monitoring of vital signs in general wards: A systematic review. [PDF]
van Zeist-de Jonge B +5 more
europepmc +1 more source
Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce +72 more
wiley +1 more source
"Validation of ultra-high dependability…" – 20 years on [PDF]
Littlewood, B., Strigini, L.
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