Results 171 to 180 of about 9,971 (245)

Four general‐purpose large language models (ChatGPT‐5, Claude 4, Grok 4 and Gemini 2.5) show comparable performance in specialised total knee arthroplasty clinical questions

open access: yesKnee Surgery, Sports Traumatology, Arthroscopy, EarlyView.
Abstract Purpose To evaluate and compare the performance of four general‐purpose large language models (LLMs) (ChatGPT‐5, Claude 4, Grok 4 and Gemini 2.5) in answering specialised clinical questions related to total knee arthroplasty (TKA) derived from the World Expert Meeting in Arthroplasty (WEMA). Methods This is a cross‐sectional comparative study.
Oriol Pujol   +7 more
wiley   +1 more source

Persistent hypervascularity of the corpus luteum in the setting of acute ovarian torsion. [PDF]

open access: yesRadiol Case Rep
Rogers D   +5 more
europepmc   +1 more source

Market Interviews in Shared Traumatic Reality: A Trauma‐Informed, Co‐Constructed Framework

open access: yesPsychology &Marketing, EarlyView.
ABSTRACT Qualitative market interviews may become trauma‐sensitive when ordinary questions about consumption, work, finance, mobility, identity, professional continuity, or institutional trust intersect with displacement, insecurity, loss, or ongoing threat.
Nataliia Kochkina   +3 more
wiley   +1 more source

FXTAS and the Spectrum of FMR1 Premutation‐Associated Phenotypes in Latin America: A Scoping Review

open access: yesMovement Disorders Clinical Practice, EarlyView.
Abstract Background Fragile X–associated tremor/ataxia syndrome (FXTAS) is a late‐onset neurodegenerative disorder caused by FMR1 premutation expansions (55–200 CGG repeats). Although well described in populations of predominantly European ancestry, FXTAS remains poorly characterized in Latin America due to limited awareness, restricted access to ...
Amy Schmidmajer   +6 more
wiley   +1 more source

Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case‐Series and Literature Review

open access: yesMovement Disorders Clinical Practice, EarlyView.
Abstract Background Variants in AFG3‐Like Matrix AAA Peptidase, Subunit 2 (AFG3L2) gene are associated with diverse clinical phenotypes. Here, we describe phenotypic findings of two unrelated children with de novo heterozygous variant and one family with inherited heterozygous variant in AFG3L2 gene.
Sangeetha Yoganathan   +14 more
wiley   +1 more source

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