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Mengchun Li

Showing results (21-30 of 48) with videos related to

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Frontiers in Aging Neuroscience|December 6, 2021
Lateralized Contributions of Medial Prefrontal Cortex Network to Episodic Memory Deficits in Subjects With Amnestic Mild Cognitive ImpairmentQing Ye, Haifeng Chen, Renyuan Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|January 8, 2025
[Clinical and genetic characteristics analysis of two children with comorbidity of two rare genetic diseases]Ling Gan, Ruirui Liang, Yueqin Li, et al.
Heliyon|September 19, 2024
Novel homozygous missense variants in <i>MED27</i> associated with neurodevelopmental disorder: Clinical and pathogenetic researchGongao Wu, Ruofei Lian, Mengchun Li, et al.
Frontiers in Aging Neuroscience|February 13, 2020
White Matter Microstructural Damage as an Early Sign of Subjective Cognitive DeclineCaimei Luo, Mengchun Li, Ruomeng Qin, et al.
Frontiers in Neuroscience|October 19, 2020
Aberrant White Matter Microstructure as a Potential Diagnostic Marker in Alzheimer's Disease by Automated Fiber QuantificationHaifeng Chen, Xiaoning Sheng, Ruomeng Qin, et al.
Epilepsia Open|November 27, 2023
Clinical and genetic analysis of infants with pontocerebellar hypoplasia type 6 caused by RARS2 variationsShichao Zhao, Ruofei Lian, Liang Jin, et al.
Frontiers in Neurology|May 22, 2023
Clinical and genetic analysis of Christianson syndrome caused by variant of <i>SLC9A6</i>: case report and literature reviewYan Dong, Ruofei Lian, Liang Jin, et al.
Clinical Pharmacology in Drug Development|December 30, 2020
Phase 1 Study of the Effects of the Tuberculosis Treatment Pretomanid, Alone and in Combination With Moxifloxacin, on the QTc Interval in Healthy VolunteersMengchun Li, George A Saviolakis, Wael El-Amin, et al.
Journal of Cellular and Molecular Medicine|July 21, 2025
ARF1-Related Diseases in China: The Initial Study of Phenotype and Molecular ProfileRuofei Lian, Gongao Wu, Liang Jin, et al.
Epilepsia Open|March 16, 2024
Analysis of clinical characteristics and histopathological transcription in 40 patients afflicted by epilepsy stemming from focal cortical dysplasiaKe Zhang, He Yao, Jixue Yang, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Frontiers in Aging Neuroscience|December 6, 2021
Lateralized Contributions of Medial Prefrontal Cortex Network to Episodic Memory Deficits in Subjects With Amnestic Mild Cognitive ImpairmentQing Ye, Haifeng Chen, Renyuan Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|January 8, 2025
[Clinical and genetic characteristics analysis of two children with comorbidity of two rare genetic diseases]Ling Gan, Ruirui Liang, Yueqin Li, et al.
Heliyon|September 19, 2024
Novel homozygous missense variants in <i>MED27</i> associated with neurodevelopmental disorder: Clinical and pathogenetic researchGongao Wu, Ruofei Lian, Mengchun Li, et al.
Frontiers in Aging Neuroscience|February 13, 2020
White Matter Microstructural Damage as an Early Sign of Subjective Cognitive DeclineCaimei Luo, Mengchun Li, Ruomeng Qin, et al.
Frontiers in Neuroscience|October 19, 2020
Aberrant White Matter Microstructure as a Potential Diagnostic Marker in Alzheimer's Disease by Automated Fiber QuantificationHaifeng Chen, Xiaoning Sheng, Ruomeng Qin, et al.
Epilepsia Open|November 27, 2023
Clinical and genetic analysis of infants with pontocerebellar hypoplasia type 6 caused by RARS2 variationsShichao Zhao, Ruofei Lian, Liang Jin, et al.
Frontiers in Neurology|May 22, 2023
Clinical and genetic analysis of Christianson syndrome caused by variant of <i>SLC9A6</i>: case report and literature reviewYan Dong, Ruofei Lian, Liang Jin, et al.
Clinical Pharmacology in Drug Development|December 30, 2020
Phase 1 Study of the Effects of the Tuberculosis Treatment Pretomanid, Alone and in Combination With Moxifloxacin, on the QTc Interval in Healthy VolunteersMengchun Li, George A Saviolakis, Wael El-Amin, et al.
Journal of Cellular and Molecular Medicine|July 21, 2025
ARF1-Related Diseases in China: The Initial Study of Phenotype and Molecular ProfileRuofei Lian, Gongao Wu, Liang Jin, et al.
Epilepsia Open|March 16, 2024
Analysis of clinical characteristics and histopathological transcription in 40 patients afflicted by epilepsy stemming from focal cortical dysplasiaKe Zhang, He Yao, Jixue Yang, et al.
Pageof 5