Results 171 to 180 of about 9,971 (245)
Adulthood as a social construct: Critical discourse analysis of transition preparation consultations for youth with chronic conditions. [PDF]
Morsa M +5 more
europepmc +1 more source
L’ASPRO : un exemple d’interface cartographique pour la consultation d’un corpus archéologique
Olivier Barge +3 more
openalex +1 more source
Cooperative Corpus Consultation for Acquisition of Adjective + Preposition Collocations
Supaporn Kulsitthiboon +1 more
openalex +2 more sources
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]
Rogers D +5 more
europepmc +1 more source
Market Interviews in Shared Traumatic Reality: A Trauma‐Informed, Co‐Constructed Framework
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
Early-Onset Hyperkinetic Movement Disorders Define the Most Severe Presentation of the ATP8A2-Related Phenotypic Spectrum. [PDF]
Bruschi F +5 more
europepmc +1 more source
FXTAS and the Spectrum of FMR1 Premutation‐Associated Phenotypes in Latin America: A Scoping Review
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
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

