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LiYing Cui

Showing results (241-250 of 323) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|October 22, 2020
Study on sleep-wake disorders in patients with genetic and non-genetic amyotrophic lateral sclerosisXiaohan Sun, Ximeng Zhao, Qing Liu, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 14, 2019
Guidelines for single fiber EMGDonald B Sanders, Kimiyoshi Arimura, LiYing Cui, et al.
Annals of Neurology|June 27, 2025
Clonal Hematopoiesis of Indeterminate Potential Associated with Covert Cerebral ChangesYijuan Li, Dingding Zhang, Fei Han, et al.
International Journal of Molecular Medicine|January 3, 2020
Construction of a long non‑coding RNA‑mediated transcription factor and gene regulatory triplet network reveals global patterns and biomarkers for ischemic strokeYuze Cao, Jianjian Wang, Xiaoyu Lu, et al.
Journal of Alzheimer'S Disease : JAD|May 2, 2022
PSEN2 Mutation Spectrum and Novel Functionally Validated Mutations in Alzheimer's Disease: Data from PUMCH Dementia CohortLiling Dong, Caiyan Liu, Longze Sha, et al.
Frontiers in Immunology|August 28, 2020
Study of B Cell Repertoire in Patients With Anti-N-Methyl-D-Aspartate Receptor EncephalitisJingjing Feng, Siyuan Fan, Yinwei Sun, et al.
Clinical Neurology and Neurosurgery|November 8, 2021
A pilot study of multiple time points and multidomain assessment in cerebrospinal fluid tap test for patients with idiopathic normal pressure hydrocephalusCaiyan Liu, Liling Dong, Jie Li, et al.
Multiple Sclerosis and Related Disorders|November 19, 2018
Acute epileptic seizures in myelin oligodendrocyte glycoprotein encephalomyelitis and neuromyelitis optica spectrum disorder: A comparative cohort studyYuan Yao, Yan Xu, Haitao Ren, et al.
Journal of Neurology|June 19, 2024
Clinical and genetic characteristics of 1672 cases of amyotrophic lateral sclerosis in China: a single-center retrospective studyDongchao Shen, Xunzhe Yang, Di He, et al.
Human Mutation|November 10, 2019
Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophiesChao Ling, Yi Dai, Li Fang, et al.
Pageof 33

Showing results (241-250 of 323) with videos related to

Sort By:
Pageof 33
Journal of Neurology, Neurosurgery, and Psychiatry|October 22, 2020
Study on sleep-wake disorders in patients with genetic and non-genetic amyotrophic lateral sclerosisXiaohan Sun, Ximeng Zhao, Qing Liu, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 14, 2019
Guidelines for single fiber EMGDonald B Sanders, Kimiyoshi Arimura, LiYing Cui, et al.
Annals of Neurology|June 27, 2025
Clonal Hematopoiesis of Indeterminate Potential Associated with Covert Cerebral ChangesYijuan Li, Dingding Zhang, Fei Han, et al.
International Journal of Molecular Medicine|January 3, 2020
Construction of a long non‑coding RNA‑mediated transcription factor and gene regulatory triplet network reveals global patterns and biomarkers for ischemic strokeYuze Cao, Jianjian Wang, Xiaoyu Lu, et al.
Journal of Alzheimer'S Disease : JAD|May 2, 2022
PSEN2 Mutation Spectrum and Novel Functionally Validated Mutations in Alzheimer's Disease: Data from PUMCH Dementia CohortLiling Dong, Caiyan Liu, Longze Sha, et al.
Frontiers in Immunology|August 28, 2020
Study of B Cell Repertoire in Patients With Anti-N-Methyl-D-Aspartate Receptor EncephalitisJingjing Feng, Siyuan Fan, Yinwei Sun, et al.
Clinical Neurology and Neurosurgery|November 8, 2021
A pilot study of multiple time points and multidomain assessment in cerebrospinal fluid tap test for patients with idiopathic normal pressure hydrocephalusCaiyan Liu, Liling Dong, Jie Li, et al.
Multiple Sclerosis and Related Disorders|November 19, 2018
Acute epileptic seizures in myelin oligodendrocyte glycoprotein encephalomyelitis and neuromyelitis optica spectrum disorder: A comparative cohort studyYuan Yao, Yan Xu, Haitao Ren, et al.
Journal of Neurology|June 19, 2024
Clinical and genetic characteristics of 1672 cases of amyotrophic lateral sclerosis in China: a single-center retrospective studyDongchao Shen, Xunzhe Yang, Di He, et al.
Human Mutation|November 10, 2019
Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophiesChao Ling, Yi Dai, Li Fang, et al.
Pageof 33