Results 151 to 160 of about 1,588,723 (306)
Costo-efectividad de métodos diagnósticos en apendicitis, revisión sistemática
Revista Colombiana de CirugíaIntroducción. El diagnóstico de apendicitis puede ser difícil en algunos casos, por lo cual requiere el uso de técnicas diagnósticas tales como el ultrasonido y la tomografía computadorizada.
César Augusto Guevara +1 more
doaj
ELECTRONIC AND COMPUTER-ASSISTED STUDIES OF BIOMEDICAL PROBLEMS [PDF]
, 1965 F V Flynn
openalex +1 more source
Journal of Applied Clinical Medical Physics, EarlyView.Abstract Purpose To create and conduct a comprehensive onsite end‐to‐end dosimetry audit to assess treatment accuracy of spine, lung, and soft tissue Stereotactic Body Radiotherapy (SBRT) across Australian and New Zealand (ANZ) radiotherapy centers. Methods The Australian Clinical Dosimetry Service (ACDS) anthropomorphic thorax phantom underwent a CT ...
Maddison Shaw +8 more
wiley +1 more source
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations
Annals of Clinical and Translational Neurology, EarlyView.Abstract Neuromuscular features are common in mitochondrial DNA (mtDNA) disorders. The genetic architecture of mtDNA disorders in diverse populations is poorly understood. We analysed mtDNA variants from whole‐exome sequencing data in neuromuscular patients from South Africa, Brazil, India, Turkey and Zambia. In 998 individuals, there were two definite
Fei Gao +34 more
wiley +1 more source
Adaptation of Biomedical and Clinical Pretrained Models to French Long Documents: A Comparative Study [PDF]
arXivRecently, pretrained language models based on BERT have been introduced for the French biomedical domain. Although these models have achieved state-of-the-art results on biomedical and clinical NLP tasks, they are constrained by a limited input sequence length of 512 tokens, which poses challenges when applied to clinical notes.
arxiv
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra +17 more
wiley +1 more source
BMRetriever: Tuning Large Language Models as Better Biomedical Text Retrievers [PDF]
EMNLP 2024Developing effective biomedical retrieval models is important for excelling at knowledge-intensive biomedical tasks but still challenging due to the deficiency of sufficient publicly annotated biomedical data and computational resources. We present BMRetriever, a series of dense retrievers for enhancing biomedical retrieval via unsupervised pre ...
arxiv