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Current Microbiology|January 6, 2025
Diversity of Soil Microbial Communities in the Bulk and Rhizosphere Soils of Acanthopanax senticosus in Different HabitatsWenhui Yuan, Deqiang Yang, Zhipeng Xu, et al.Genes|May 28, 2022
Novel Loss-of-Function Variants in CHD2 Cause Childhood-Onset Epileptic Encephalopathy in Chinese PatientsXu Wang, Di Cui, Changhong Ding, et al.Pediatric Neurology|April 10, 2021
Clinical Features and Outcomes of Anti-N-Methyl-d-Aspartate Receptor Encephalitis in Infants and ToddlersChanghong Ren, Weihua Zhang, Xiaotun Ren, et al.Brain & Development|May 4, 2023
The clinical spectrum associated with ATP1A2 variants in Chinese pediatric patientsLifang Dai, Changhong Ding, Xiaojuan Tian, et al.BMC Neurology|July 1, 2026
One case of acute encephalopathy associated with 16p11.2 deletion and PRRT2 gene mutationSiYu Shang, QiuHong Wang, JiaNing Wang, et al.Molecular Genetics & Genomic Medicine|February 14, 2022
Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patientsJianbo Zhao, Guizhen Lyu, Changhong Ding, et al.Clinical Neurology and Neurosurgery|May 7, 2024
Deep brain stimulation for pediatric pantothenate kinase-associated neurodegeneration with status dystonicus: A case report and literature reviewZhenhang Zhai, Ke Sun, Tinghong Liu, et al.European Journal of Medical Genetics|February 2, 2021
Novel truncating mutations in ASXL1 identified in two boys with Bohring-Opitz syndromeJianbo Zhao, Yanqi Hou, Fang Fang, et al.Pediatric Investigation|April 6, 2022
Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow-upWeihua Zhang, Jiuwei Li, Xiuwei Zhuo, et al.Journal of Human Genetics|December 17, 2010
Identification of novel MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts (MLC)Jingmin Wang, Jing Shang, Ye Wu, et al.Pageof 5