Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Zhongdong Lin"'
Autor:
Feixia Zheng, Xiaoyan Ye, Yuanyuan Chen, Hongying Wang, Shiyu Fang, Xulai Shi, Zhongdong Lin, Zhenlang Lin
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
PurposeFew studies have evaluated hyponatremia management in children with bacterial meningitis (BM). Thus, we aimed to describe variations in clinical practice, the effectiveness of sodium management, and adverse outcomes in children with BM and hyp
Externí odkaz:
https://doaj.org/article/207d8bceb5ef48f08ea2758075a86200
Autor:
Xiucui Li, Huiya Ying, Zilong Zhang, Zijing Yang, Cancan You, Xiaohong Cai, Zhongdong Lin, Yanfeng Xiao
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 16 (2022)
Obstructive sleep apnea–hypopnea syndrome (OSAHS), typically characterized by chronic intermittent hypoxia (CIH), is associated with neurocognitive dysfunction in children. Sulforaphane (SFN), an activator of nuclear factor E2-related factor 2 (Nrf
Externí odkaz:
https://doaj.org/article/552166dd8f2c46b19fd05fdbdda02f5e
Autor:
Xiucui Li, Shijia Bao, Wei Wang, Xulai Shi, Ying Hu, Feng Li, Qianlei Zhao, Feixia Zheng, Zhongdong Lin
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
A series of neurological manifestations such as intellectual disability and epilepsy are closely related to hypomagnesemia. Cyclin M2 (CNNM2) proteins, as a member of magnesium (Mg2+) transporters, were found along the basolateral membrane of distal
Externí odkaz:
https://doaj.org/article/fd2550fd80e04575982cbb57e190107e
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract Epileptic encephalopathies (EE) are a group of severe childhood epilepsy disorders characterized by intractable seizures, cognitive impairment and neurological deficits. Recent whole-exome sequencing (WES) studies have implicated significant
Externí odkaz:
https://doaj.org/article/a1aa4273b54243acad864b1e15474333
Autor:
Qiongdan Wang, Zhenwei Liu, Zhongdong Lin, Ru Zhang, Yutian Lu, Weijue Su, Feng Li, Xi Xu, Mengyun Tu, Yongliang Lou, Junzhao Zhao, Xiaoqun Zheng
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Infantile spasm (IS) is an early-onset epileptic encephalopathy that usually presents with hypsarrhythmia on an electroencephalogram with developmental impairment or regression. In this study, whole-exome sequencing was performed to detect potential
Externí odkaz:
https://doaj.org/article/4eee9baa4ec841edb4fbdb3dc134eda9
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Background: Hyponatremia has frequently been described as a common complication associated with bacterial meningitis, though its frequency and clinical course in children with bacterial meningitis are unclear. The present study aimed to investigate t
Externí odkaz:
https://doaj.org/article/6581bfb86b3b4b328554bfd3fc5627ae
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
The use of botulinum neurotoxin serotype A (BoNT-A) injections for the treatment of orofacial dyskinesia secondary to anti-N-methyl-d-aspartate receptor (NMDAR) encephalitis is rarely reported. Here, we report a case of an urgent, successful manageme
Externí odkaz:
https://doaj.org/article/34fa9c7b16b94a2f9adbbb615e87478d
Autor:
Qianlei Zhao, Tingting Chen, Chao Ni, Yingying Hu, Yan Nan, Wei Lin, Yanli Liu, Feixia Zheng, Xulai Shi, Zhongdong Lin, Jianghu Zhu, Zhenlang Lin
Publikováno v:
ACS Chemical Neuroscience. 13:2897-2912
The blood-brain barrier (BBB) is an important physiological barrier of the human body contributing to maintaining brain homeostasis and normal function. Hypoxic-ischemic (HI)-related brain injury is one of the main causes of neonatal acute morbidity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49d9c039bf09c0c5ff1de76e7658406f
https://doi.org/10.1021/acschemneuro.2c00418
https://doi.org/10.1021/acschemneuro.2c00418
Publikováno v:
Journal of Clinical Medicine; Volume 12; Issue 2; Pages: 473
Cerebral adrenoleukodystrophy (CALD) is a fatal genetic disease characterized by rapid, devastating neurological decline, with a narrow curative treatment window in the early stage. Non-canonical splice-site (NCSS) variants can easily be missed durin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::764266b2096480675deaa41ca0323510
Autor:
Ying Hu, Zhenwei Liu, Feixia Zheng, Shiyu Fang, Zhongdong Lin, Qianlei Zhao, Feng Li, Xiucui Li
Publikováno v:
Acta Neurologica Belgica
To analyze the clinical characteristics and PRRT2 gene mutation of self-limited familial infantile epilepsy and evaluate the treatment responses of different antiepileptic drugs in self-limited familial infantile epilepsy. We reviewed the clinical fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc1360f576be29297736906e7ffc28bc
https://doi.org/10.1007/s13760-020-01348-9
https://doi.org/10.1007/s13760-020-01348-9