Results 131 to 140 of about 2,402,901 (306)

Large Language Models Enhance Molecular Diagnoses of Mendelian Disorders via A Novel Logic [PDF]

Zefu Chen, Jihao Cai, Yongxin Yang, Sen Zhao, G Z Li, Kexin Xu, Qing Li, Timothy Hospedales, Lina Zhao, Zhongmin Zhang, Zhihong Wu, Guixing Qiu, Jianguo Zhang, Pengfei Liu, Ni Wu   +14 more
openalex   +1 more source

Variably Protease‐Sensitive Prionopathy: Two New Cases With Motor Neuron‐Dementia Syndrome

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT We describe two patients with variably protease‐sensitive prionopathy (VPSPr) who developed progressive upper motor neuron symptoms, insomnia, behavioral and cognitive decline, compatible with primary lateral sclerosis associated with frontotemporal dementia (FTD).
María Elena Erro, María Victoria Zelaya, Hasier Eraña, Javier Sánchez Ruiz de Gordoa, Fermín García‐Amigot, Anika Simonovska‐Serra, María Cristina Caballero, Isidre Ferrer, Ellen Gelpi, Ivonne Jericó, Joaquín Castilla   +10 more
wiley   +1 more source

Efficient multimodal large language models: a survey

Visual Intelligence
In the past years, multimodal large language models (MLLMs) have demonstrated remarkable performance in tasks such as visual question answering and visual understanding and reasoning.
Yizhang Jin, Jian Li, Tianjun Gu, Yexin Liu, Bo Zhao, Jinxiang Lai, Zhenye Gan, Yabiao Wang, Chengjie Wang, Xin Tan, Lizhuang Ma   +10 more
doaj   +1 more source

Patterns of Postictal Abnormalities in Relation to Status Epilepticus in Adults

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Abnormalities on peri‐ictal diffusion‐weighted magnetic resonance imaging (DWI‐PMAs) are well‐established for patients with status epilepticus (SE), but knowledge on patterns of DWI‐PMAs and their prognostic impact is sparse. Methods This systematic review and individual participant data meta‐analysis included observational studies ...
Andrea Enerstad Bolle, Silvana Sarria‐Estrada, Thomas Bonduelle, Bertram Daniel Dynesen, Manuel Toledo, Zhu Chung Che, Kjell Heuser, Anastasios Chatzikonstantinou, Jérôme Aupy, Udaya Seneviratne, Estevo Santamarina Perez, Christoph Patrick Beier   +11 more
wiley   +1 more source

XAI for All: Can Large Language Models Simplify Explainable AI? [PDF]

Philip Mavrepis, Georgios Makridis, Georgios Fatouros, Vasileios Koukos, Maria Margarita Separdani, Dimosthenis Kyriazis   +5 more
openalex   +1 more source

A Survey on Multimodal Large Language Models for Autonomous Driving [PDF]

, 2023
Can Cui, Yunsheng Ma, Xu Cao, Wenqian Ye, Yang Zhou, Kaizhao Liang, Jintai Chen, Juanwu Lu, Zichong Yang, Kuei-Da Liao, Tianren Gao, Erlong Li, Tang Kun, Zhipeng Cao, Tong Zhou, Ao Liu, Xinrui Yan, Shuqi Mei, Jianguo Cao, Ziran Wang, Chao Zheng   +20 more
openalex   +1 more source

Real‐World Performance of CSF Kappa Free Light Chains in the 2024 McDonald Criteria

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Kappa free light chains (KFLCs) in the cerebrospinal fluid (CSF) have a similar performance to CSF‐restricted oligoclonal bands (OCB) for multiple sclerosis (MS) diagnosis. To help with implementation, we set out to resolve several remaining uncertainties: (1) performance in a real‐world cohort and the 2024 McDonald criteria; (2 ...
Maya M. Leibowitz, Ryan Cooper, Stefania Kaninia, Kathryn I. Challis, Will Greenway, Maria Bonello, Mahmoud Elbahnasawi, Deborah T. Shode, Dominika Gajdasik, Victor Iliev, Alison M. E. Whitelegg, Ian Galea   +11 more
wiley   +1 more source

Modeling meets Large Language Models

Modeling business processes is often challenging due to its complexity and potential for errors. One key issue arises when process experts and modelers are different individuals, which can lead to communication gaps and result in low-quality business process models.
Forell, Martin, Schüler, Selina
openaire   +2 more sources

Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Adrenoleukodystrophy is a rare inherited peroxisomal disease caused by pathogenic variants in the ABCD1 gene located on the X chromosome. Although the most severe central nervous system and adrenal complications typically affect only men with adrenoleukodystrophy, the majority of women develop myeloneuropathy symptoms in adulthood.
Chenwei Yan, Elizabeth I. Pierpont, Amena S. Fine, Reena V. Kartha   +3 more
wiley   +1 more source

Large language models and scientific publishing

Journal of Data and Information Science, 2023
Rousseau Ronald, Yang Liying, Bollen Johan, Shen Zhesi   +3 more
doaj   +1 more source