Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Feixia Zheng"'
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
BackgroundMinichromosome maintenance complex component 3 associated protein (MCM3AP) is a gene in which mutations can result in autosomal recessive peripheral neuropathy with or without impaired intellectual development. The MCM3AP genotype-phenotype
Externí odkaz:
https://doaj.org/article/7ba71d69c92345e4872e62010204053d
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, 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:
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:
Molecular Genetics and Metabolism Reports, Vol 5, Iss C, Pp 80-84 (2015)
We report an 8-year-old girl with lower limb weakness since birth in whom mitochondrial trifunctional protein (MTP) deficiency, an autosomal recessive fatty acid oxidation disorder caused by HADHA or HADHB mutations, had not been definitively diagnos
Externí odkaz:
https://doaj.org/article/676dd7fffb7b428d9276650769d0c387
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
Autor:
Ying Hu, Xu-Lai Shi, Feng Li, Shijia Bao, Wei Wang, Xiucui Li, Qianlei Zhao, Feixia Zheng, Zhongdong Lin
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics
Frontiers in Genetics
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a0aa8139312e6a483217e76d99a4ccd
https://www.frontiersin.org/articles/10.3389/fgene.2021.705734/full
https://www.frontiersin.org/articles/10.3389/fgene.2021.705734/full