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Oncology Letters|April 5, 2019
Pharmacokinetic analysis for the differentiation of pituitary microadenoma subtypes through dynamic contrast-enhanced magnetic resonance imagingJian Zhai, Wenqiang Zheng, Qin Zhang, et al.
Journal of Magnetic Resonance Imaging : JMRI|November 16, 2018
A Triple-Classification Radiomics Model for the Differentiation of Primary Chordoma, Giant Cell Tumor, and Metastatic Tumor of Sacrum Based on T2-Weighted and Contrast-Enhanced T1-Weighted MRIPing Yin, Ning Mao, Chao Zhao, et al.
Hemoglobin|February 29, 2024
Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid DifferentiationDan Xie, Yuanyuan Han, Wenyi Zhang, et al.
Journal of Clinical Medicine|August 12, 2022
Swin Transformer Improves the IDH Mutation Status Prediction of Gliomas Free of MRI-Based Tumor SegmentationJiangfen Wu, Qian Xu, Yiqing Shen, et al.
European Radiology|October 4, 2018
Comparison of radiomics machine-learning classifiers and feature selection for differentiation of sacral chordoma and sacral giant cell tumour based on 3D computed tomography featuresPing Yin, Ning Mao, Chao Zhao, et al.
Biomed Research International|May 29, 2020
Differentiation of Pelvic Osteosarcoma and Ewing Sarcoma Using Radiomic Analysis Based on T2-Weighted Images and Contrast-Enhanced T1-Weighted ImagesYi Dai, Ping Yin, Ning Mao, et al.
Medicine|February 3, 2018
Tumor recurrence versus treatment effects in glioma: A comparative study of three dimensional pseudo-continuous arterial spin labeling and dynamic susceptibility contrast imagingQian Xu, Qi Liu, Haitao Ge, et al.
International Journal of Computer Assisted Radiology and Surgery|September 18, 2014
Resting state fMRI feature-based cerebral glioma grading by support vector machineJiangfen Wu, Zhiyu Qian, Ling Tao, et al.
Medicine|February 17, 2023
A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case reportDan Xie, Jiangfen Wu, Wenyi Zhang, et al.
Journal of Clinical Laboratory Analysis|July 15, 2022
Whole-exome sequencing identified five novel de novo variants in patients with unexplained intellectual disabilityWenqiu Zhang, Li Hu, Xinyi Huang, et al.
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