Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jiuwei Li

Showing results (11-20 of 45) with videos related to

Pageof 5
Sort By:
Frontiers in Genetics|November 28, 2022
Immunogenic cell death-related classifications in breast cancer identify precise immunotherapy biomarkers and enable prognostic stratificationXue Wang, Hailiang Huang, Xijian Liu, 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.
Biochemical and Biophysical Research Communications|March 9, 2020
MiR-429 regulates blood-spinal cord barrier permeability by targeting Krüppel-like factor 6Rui Sun, Lihao Ge, Yang Cao, et al.
Biochemical and Biophysical Research Communications|May 23, 2020
Corrigendum to "MiR-429 regulates blood-spinal cord barrier permeability by targeting Krüppel-like factor 6" [Biochem. Biophys. Res. Commun.(2020)]Rui Sun, Lihao Ge, Yang Cao, et al.
Pediatric Neurology|November 22, 2025
Mycoplasma Pneumoniae-Associated Arterial Ischemic Stroke in Pediatric Patients: Clinical Manifestations and Neuroimaging FindingsZemou Yu, Lingbing Meng, Jingjing Jia, et al.
Pediatric Radiology|April 13, 2024
Diagnostic value of <sup>18</sup>F-fluorodeoxyglucose positron emission tomography/computed tomography imaging in pediatric opsoclonus myoclonus ataxia syndrome presenting with neuroblastomaLijuan Feng, Shen Yang, Yu Lin, 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.
Brain & Development|May 30, 2017
WITHDRAWN: Clinical and molecular analysis of six novel GALC mutations identified in 7 Chinese children with Krabbe diseaseLifang Dai, Tongli Han, Xinying Yang, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|March 20, 2021
Report of a case with ferredoxin reductase (FDXR) gene variants in a Chinese boy exhibiting hearing loss, visual impairment, and motor retardationChengqing Yang, Ying Zhang, Jiuwei Li, et al.
Seizure|June 4, 2026
The electroencephalographic patterns in the acute phase of febrile infection related epilepsy syndrome in childrenXiaojuan Tian, Yan Li, Hua Li, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Frontiers in Genetics|November 28, 2022
Immunogenic cell death-related classifications in breast cancer identify precise immunotherapy biomarkers and enable prognostic stratificationXue Wang, Hailiang Huang, Xijian Liu, 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.
Biochemical and Biophysical Research Communications|March 9, 2020
MiR-429 regulates blood-spinal cord barrier permeability by targeting Krüppel-like factor 6Rui Sun, Lihao Ge, Yang Cao, et al.
Biochemical and Biophysical Research Communications|May 23, 2020
Corrigendum to "MiR-429 regulates blood-spinal cord barrier permeability by targeting Krüppel-like factor 6" [Biochem. Biophys. Res. Commun.(2020)]Rui Sun, Lihao Ge, Yang Cao, et al.
Pediatric Neurology|November 22, 2025
Mycoplasma Pneumoniae-Associated Arterial Ischemic Stroke in Pediatric Patients: Clinical Manifestations and Neuroimaging FindingsZemou Yu, Lingbing Meng, Jingjing Jia, et al.
Pediatric Radiology|April 13, 2024
Diagnostic value of <sup>18</sup>F-fluorodeoxyglucose positron emission tomography/computed tomography imaging in pediatric opsoclonus myoclonus ataxia syndrome presenting with neuroblastomaLijuan Feng, Shen Yang, Yu Lin, 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.
Brain & Development|May 30, 2017
WITHDRAWN: Clinical and molecular analysis of six novel GALC mutations identified in 7 Chinese children with Krabbe diseaseLifang Dai, Tongli Han, Xinying Yang, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|March 20, 2021
Report of a case with ferredoxin reductase (FDXR) gene variants in a Chinese boy exhibiting hearing loss, visual impairment, and motor retardationChengqing Yang, Ying Zhang, Jiuwei Li, et al.
Seizure|June 4, 2026
The electroencephalographic patterns in the acute phase of febrile infection related epilepsy syndrome in childrenXiaojuan Tian, Yan Li, Hua Li, et al.
Pageof 5