Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Wuqiong Zhang"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Oxidative stress causes diverse neurological disorders. Parthanatos is a type of programmed cell death, characterised by strong activation of poly (ADP-ribose) (PAR) polymerase-1 (PARP-1), PAR polymer accumulation, and nuclear translocation
Externí odkaz:
https://doaj.org/article/b79a7022ddbd4a6cb08f9a4037247ba9
Autor:
Zhiqing Chen, Yujin Guo, Huaiyu Sun, Wuqiong Zhang, Shuai Hou, Yu Guo, Xiaohui Ma, Hongmei Meng
Publikováno v:
Frontiers in Aging Neuroscience, Vol 16 (2024)
BackgroundAn increasing body of research has demonstrated a robust correlation between circulating inflammatory proteins and neuromyelitis optica spectrum disorders (NMOSD). However, whether this association is causal or whether immune cells act as m
Externí odkaz:
https://doaj.org/article/95937200076449dcba1295fea6d8538e
Publikováno v:
Frontiers in Neurology, Vol 14 (2024)
Blepharospasm is a focal dystonia characterized by involuntary tetanic contractions of the orbicularis oculi muscle, which can lead to functional blindness and loss of independent living ability in severe cases. It usually occurs in adults, with a hi
Externí odkaz:
https://doaj.org/article/a5c5349e6fe34b13935a0da8547f3bf1
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
IntroductionThe causal relationship between inflammatory factors and stroke subtypes remains unclear. This study aimed to analyze the causal relationship between 41 inflammatory factors and these two factors using Mendelian randomization (MR).Methods
Externí odkaz:
https://doaj.org/article/ea1a05daa63c414b9cdb0c8c7c85e189
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
BackgroundLeukodystrophies are hereditary white matter diseases characterized by genetic polymorphisms and considerable phenotypic variability. They can be classified into myelin and non-myelin malformations. These diseases are rare, affecting 1 out
Externí odkaz:
https://doaj.org/article/d4c98f8031f849f99b806fadc86c42cc
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Objectives: The present study explored the clinical characteristics and prognostic factors of epilepsy in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS).Methods: Thirty-four MELAS patients were includ
Externí odkaz:
https://doaj.org/article/04ac3af3054b474db8db1934ddc7c8c3
Publikováno v:
Frontiers in Neurology, Vol 11 (2021)
Glucose transporter type 1 deficiency syndrome (Glut1-DS) is a rare neurometabolic disorder caused by mutations of the SLC2A1 gene. Paroxysmal exercise-induced dyskinesia is regarded as a representative symptom of Glut1-DS. Paroxysmal non-kinesigenic
Externí odkaz:
https://doaj.org/article/66cf632975134ab1ada28b20b28e6ee8
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 266-267 (2021)
Externí odkaz:
https://doaj.org/article/f87c5df9a90041acb75f60747bd87ae1
Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Familial hemiplegic migraine (FHM) is a rare, monogenic, autosomal dominant subtype of migraine, in which three genes, CACNA1A, ATP1A2, and SCN1A, are currently known to be involved. The familial hemiplegic migraine type 3 (FHM3) is seldom caused by
Externí odkaz:
https://doaj.org/article/309aae8f7c0843b1a75f7cb2fd1d6a62
Autor:
Wuqiong Zhang1, Xiaojuan Ye2, Hongmei Meng1 hongmeiyp@126.com, Zhang, Wuqiong1 (AUTHOR), Ye, Xiaojuan2 (AUTHOR), Meng, Hongmei1 (AUTHOR)
Publikováno v:
Neurology India. Sep/Oct2022, Vol. 70 Issue 5, p2100-2105. 7p.