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Journal of Interventional Medicine|November 22, 2021
A case of spontaneous hepatic hemangioma rupture: Successful management with transarterial chemoembolization aloneYanyan Cao, Fu Xiong, Bin Xiong, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 1, 2022
[Clinical significance of serum miRNA-146, OX-LDL and ROS expression in patients with primary ovarian insufficiency]Yanhui Liu, Jia'nan Liu, Fu Xiong, et al.
Hepatology International|August 20, 2021
Efficacy of apatinib in patients with sorafenib-transarterial chemoembolization refractory hepatocellular carcinoma: a retrospective studyYanyan Cao, Tao Ouyang, Fu Xiong, et al.
Global Medical Genetics|April 10, 2026
Molecular mechanism study of novel compound heterozygous EOGT mutations leading to Adams-Oliver syndrome type 4Yufei He, Xiangyu Liu, Zongrui Shen, et al.
Frontiers in Genetics|July 12, 2021
Case Report: A Novel <i>COL1A1</i> Missense Mutation Associated With Dentineogenesis Imperfecta Type IYuting Zeng, Yuhua Pan, Jiayao Mo, et al.
Ying Yong Sheng Tai Xue Bao = the Journal of Applied Ecology|August 5, 2011
[Effects of extreme drought on plant species in Karst area of Guizhou Province, Southwest China]Hong-Fu Xiong, Shi-Jie Wang, Li Rong, et al.
Experimental and Therapeutic Medicine|January 18, 2019
Two successive cases of fetal harlequin ichthyosis: A case reportQianhong Liang, Fu Xiong, Xuankun Liang, et al.
Blood Cells, Molecules & Diseases|July 15, 2010
Analysis of alpha-hemoglobin-stabilizing protein (AHSP) gene as a genetic modifier to the phenotype of beta-thalassemia in Southern ChinaZhipeng Wang, Wenfang Yu, Ying Li, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|September 14, 2007
A method comparison in monitoring disease progression of G93A mouse model of ALSChang Zhou, Cui-Ping Zhao, Chen Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 6, 2026
[Genetic analysis of a fetus with renal dysplasia/hypoplasia due to a variant of GREB1L gene and literature review]Danning Ma, Shunfei Ma, Xiangyu Liu, et al.
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