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European Journal of Nuclear Medicine and Molecular Imaging|June 27, 2020
Usefulness of [68Ga]Ga-DOTA-FAPI-04 PET/CT in patients presenting with inconclusive [18F]FDG PET/CT findingsHaojun Chen, Liang Zhao, Dan Ruan, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 16, 2021
Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a familyWen Wei, Xiu-Fen Zheng, Dan-Dan Ruan, et al.
Frontiers in Genetics|August 26, 2024
Analyzing three pedigrees in X-linked Alport syndrome with the presentation of nephrotic syndromeJian-Hui Zhang, Jie Liu, Dan-Dan Ruan, et al.
Biomed Research International|May 28, 2021
Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 MutationsJian-Hui Zhang, Dan-Dan Ruan, Ya-Nan Hu, et al.
Cardiology Research and Practice|May 9, 2022
Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5AYao-Bin Zhu, Jian-Hui Zhang, Yuan-Yuan Ji, et al.
IEEE Transactions on Bio-Medical Engineering|February 1, 2017
Terahertz Imaging of Cutaneous Edema: Correlation With Magnetic Resonance Imaging in Burn WoundsNeha Bajwa, Shijun Sung, Daniel B Ennis, et al.
Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica|May 30, 2024
[Anti-tumor mechanism of total saponins of Paridis Rhizoma on inducing ferroptosis of breast cancer MCF-7 cells]Yi-Bo Zhang, Hui-Zhong Zhang, Yi-Dan Ruan, et al.
World Journal of Clinical Cases|December 21, 2020
Genetic diagnosis history and osteoarticular phenotype of a non-transfusion secondary hemochromatosisDan-Dan Ruan, Yu-Mian Gan, Tao Lu, et al.
Frontiers in Pediatrics|May 23, 2022
Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 VariantRuo-Li Wang, Dan-Dan Ruan, Ya-Nan Hu, et al.
The Journal of Gene Medicine|November 17, 2021
A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiencyYa-Nan Hu, Yu-Mian Gan, Yan-Ping Zhang, et al.
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