Results 151 to 160 of about 401,731 (236)

Multiple choice questions on Rheumatology

Journal of Mahatma Gandhi Institute of Medical Sciences, 2014
doaj  

Human Expertise Outperforms Artificial Intelligence in Medical Education Assessments: MCQ Creation Highlights the Irreplaceable Role of Teachers

Avicenna Journal of Medicine
Aliya Mufti, Kashif Ali, Gaurav Sharma, Mohammad Saleem   +3 more
doaj   +1 more source

Comparative Assessment of Large Language Models in Optics and Refractive Surgery: Performance on Multiple-Choice Questions. [PDF]

Vision (Basel)
Attal L, Shvartz E, Gorenshtein A, Pincovich S, Bahir D.   +4 more
europepmc   +1 more source

A Two‐Stage Questionnaire and Actigraphy Screening for iRBD in a Multicenter Retrospective Cohort

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Isolated rapid‐eye‐movement sleep behavior disorder is a prodromal marker of synucleinopathies. However, most cases remain undiagnosed due to the insufficient predictive value of questionnaires and limited access to confirmatory video‐polysomnography. We assessed a two‐stage screening strategy combining a brief questionnaire on rapid‐
Caleb A. Massimi, Giorgio Ricciardiello Mejia, Andre Metzger, Kang Hyun Ryu, Salonee Marwaha, Eva Grzegorczyk, Li Zhou, Eliana Jacobs, Boris Gilyadov, Claudia Kunney, Liqhwa Ncube, Ankit Parekh, Emmanuel Mignot, Fanny M. Elahi, Joseph Winer, Kathleen Poston, Andreas Brink‐Kjaer, Emmanuel H. During   +17 more
wiley   +1 more source

The use of large language models in generating multiple choice questions for health professions education: A systematic review and network meta-analysis. [PDF]

PLoS One
Riehm L, Nanji K, Lakhani M, Pankiv E, Hasanee D, Pfeifer W.   +5 more
europepmc   +1 more source

White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Recent evidence indicates that epilepsy is associated with abnormal white matter. If seizures alter white matter, then the impact upon network function, epileptogenesis, and cognition could be pronounced in neonates undergoing rapid developmental myelination. Neonates with epilepsy due to nonstructural genetic causes provide a unique
Amanda G. Sandoval Karamian, Tianjia Zhu, Hao Huang, Shavonne L. Massey, Mark P. Fitzgerald, Darshana Parikh, Arastoo Vossough, Ingo Helbig, Nicholas S. Abend   +8 more
wiley   +1 more source

Quantifying the speed-accuracy trade-off of large language models on oral and maxillofacial surgery multiple-choice questions. [PDF]

Sci Rep
Nguyen VA, Ha TBN, Tran MN, Pham NTM, Nguyen TL, Vuong TQT.   +5 more
europepmc   +1 more source

Subclinical Optic Nerve Involvement in Radiologically Isolated Syndrome: Multimodal Detection and Diagnostic Impact

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives We aimed to determine the frequency of subclinical optic nerve (ON) lesions using MRI, optical coherence tomography (OCT), and visual evoked potentials (VEP) in radiologically isolated syndrome (RIS), and to assess their diagnostic and prognostic significance.
Christine Lebrun‐Frenay, Cassandre Landes‐Château, Lydiane Mondot, Mikael Cohen, Margherita Popolo, Jérôme de Seze, Bertrand Bourre, Françoise Durand‐Dubief, Olivier Casez, Orhun H. Kantarci, Aksel Siva, Stephanie Baillif, Darin T. Okuda, Letizia Leocani   +13 more
wiley   +1 more source

Leveraging Large Language Models to Generate Multiple-Choice Questions for Ophthalmology Education.

JAMA Ophthalmol
Gholami S, Mummert DB, Wilson B, Page S, Dodhia R, Lavista Ferres JM, Weeks WB, Fajardo DE, Bojikian KD.   +8 more
europepmc   +1 more source

Prominent Movement Disorders in RNU2‐2‐Related Spliceosomopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Pediatric movement disorders often overlap with neurodevelopmental diseases, suggesting shared molecular mechanisms. Variants in small nuclear RNA (snRNA) genes encoding spliceosome components have recently been associated with neurodevelopmental disorders, termed “RNUopathies.” We analyzed genome sequencing data from 14 patients with ...
Magdalena Krygier, Ugo Sorrentino, Matias Wagner, Marta Zawadzka, Anna Lemska, Maria Mazurkiewicz‐Bełdzińska, Michael Zech   +6 more
wiley   +1 more source