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Qingyun Kang

Showing results (1-10 of 18) with videos related to

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Medicine|October 19, 2021
MORC2 gene de novo mutation leads to Charcot-Marie-Tooth disease type 2Z: A pediatric case report and literature reviewHaiyan Yang, Sai Yang, Qingyun Kang, et al.
Materials Science & Engineering. C, Materials for Biological Applications|December 1, 2020
Self-assembled nanogels of luminescent thiolated silver nanoclusters and chitosan as bactericidal agent and bacterial sensorJing Liu, Lina Liu, Siheng Li, et al.
Frontiers in Neurology|May 20, 2024
Clinical analysis and literature review of two paediatric cases of anti-IgLON5 antibody-related encephalitisMei Feng, Zhen Zhou, Qingyun Kang, et al.
Frontiers in Pediatrics|July 25, 2022
Clinical Characteristics and Short-Term Prognosis of Children With Antibody-Mediated Autoimmune Encephalitis: A Single-Center Cohort StudyQingyun Kang, Hongmei Liao, Liming Yang, et al.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi = Journal of Biomedical Engineering = Shengwu Yixue Gongchengxue Zazhi|May 24, 2012
[Effects of electrode on epileptogenic focus potential and expressions of the beta subunit of ATP synthase in rats with penicillin-induced epilepsy]Guohua He, Wen Zheng, Qingyun Kang, et al.
Frontiers in Neurology|January 22, 2024
Clinical characteristics of Chinese pediatric patients positive for anti-NMDAR and MOG antibodies: a case seriesQingyun Kang, Hui Kang, Shulei Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 27, 2023
[Analysis of clinical phenotype and genetic variants in a child with mitochondrial F-S disease due to variants of FDXR gene]Wenjing Hu, Xiuxin Ling, Hongjun Fang, et al.
Frontiers in Neuroscience|May 27, 2024
Clinical and genetic analyses of APMR4 syndrome caused by novel biallelic <i>LSS</i> variantsQingyun Kang, Hui Kang, Jingwen Tang, et al.
BMC Pediatrics|June 2, 2021
A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case reportQingyun Kang, Liming Yang, Hongmei Liao, et al.
Frontiers in Immunology|May 8, 2023
Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort studyQingyun Kang, Hongmei Liao, Liming Yang, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Medicine|October 19, 2021
MORC2 gene de novo mutation leads to Charcot-Marie-Tooth disease type 2Z: A pediatric case report and literature reviewHaiyan Yang, Sai Yang, Qingyun Kang, et al.
Materials Science & Engineering. C, Materials for Biological Applications|December 1, 2020
Self-assembled nanogels of luminescent thiolated silver nanoclusters and chitosan as bactericidal agent and bacterial sensorJing Liu, Lina Liu, Siheng Li, et al.
Frontiers in Neurology|May 20, 2024
Clinical analysis and literature review of two paediatric cases of anti-IgLON5 antibody-related encephalitisMei Feng, Zhen Zhou, Qingyun Kang, et al.
Frontiers in Pediatrics|July 25, 2022
Clinical Characteristics and Short-Term Prognosis of Children With Antibody-Mediated Autoimmune Encephalitis: A Single-Center Cohort StudyQingyun Kang, Hongmei Liao, Liming Yang, et al.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi = Journal of Biomedical Engineering = Shengwu Yixue Gongchengxue Zazhi|May 24, 2012
[Effects of electrode on epileptogenic focus potential and expressions of the beta subunit of ATP synthase in rats with penicillin-induced epilepsy]Guohua He, Wen Zheng, Qingyun Kang, et al.
Frontiers in Neurology|January 22, 2024
Clinical characteristics of Chinese pediatric patients positive for anti-NMDAR and MOG antibodies: a case seriesQingyun Kang, Hui Kang, Shulei Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 27, 2023
[Analysis of clinical phenotype and genetic variants in a child with mitochondrial F-S disease due to variants of FDXR gene]Wenjing Hu, Xiuxin Ling, Hongjun Fang, et al.
Frontiers in Neuroscience|May 27, 2024
Clinical and genetic analyses of APMR4 syndrome caused by novel biallelic <i>LSS</i> variantsQingyun Kang, Hui Kang, Jingwen Tang, et al.
BMC Pediatrics|June 2, 2021
A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case reportQingyun Kang, Liming Yang, Hongmei Liao, et al.
Frontiers in Immunology|May 8, 2023
Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort studyQingyun Kang, Hongmei Liao, Liming Yang, et al.
Pageof 2