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Frontiers in Neurology|November 12, 2019
SCN4A p.R675Q Mutation Leading to Normokalemic Periodic Paralysis: A Family Report and Literature ReviewJiejing Shi, Qianqian Qu, Haiyan Liu, et al.Molecular Medicine Reports|June 8, 2019
Identification of diagnostic long non‑coding RNA biomarkers in patients with hepatocellular carcinomaGang Li, Hao Shi, Xinyi Wang, et al.Frontiers in Integrative Neuroscience|February 8, 2021
Case Report: PNPLA2 Gene Complex Heterozygous Mutation Leading to Neutral Lipid Storage Disease With MyopathyJiejing Shi, Qianqian Qu, Haiyan Liu, et al.Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|October 8, 2019
C₁₈H₁₇NO₆ Inhibits Invasion and Migration of Human MNNG Osteosarcoma Cells via the PI3K/AKT Signaling PathwayQianqian Qu, Zhongshun He, Yulei Jiang, et al.Frontiers in Neurology|December 17, 2020
The Novel Compound Heterozygous Mutations in the AGL Gene in a Chinese Family With Adult Late-Onset Glycogen Storage Disease Type IIIaQianqian Qu, Qi Qian, Jiejing Shi, et al.BMC Neurology|February 17, 2026
Clinical outcomes, serum IgG changes, and follow-up observations in the treatment of anti-AChR antibody-positive generalized myasthenia gravis with EfgartigimodJingting Fu, Xianzhao Zheng, Xiaoli Ma, et al.Infectious Agents and Cancer|May 9, 2025
Tumor-infiltrating CD4+ CD25+ FOXP3+ Treg is associated with plasma EBV DNA and disease progression in nasopharyngeal carcinomaEnzi Feng, Yaoyu Yang, Jie Yang, et al.Frontiers in Neurology|October 3, 2024
Clinical, myopathological, and genetic features of two Chinese families with Andersen-Tawil syndromeJiaxuan Wang, Qianqian Qu, Xianzhao Zheng, et al.Brain and Behavior|June 14, 2021
The degeneration changes of basal forebrain are associated with prospective memory impairment in patients with Wilson's diseaseYutong Wu, Sheng Hu, Yi Wang, et al.Pageof 2