Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Fei Yin"'
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-5 (2020)
BMC Medical Genetics
BMC Medical Genetics
Background Cerebral folate deficiency (CFD) is a neurological disease, hallmarked by remarkable low concentrations of 5-methyltetrahydrofolic acid (5-MTHF) in cerebrospinal fluid (CSF). The primary causes of CFD include the presence of folate recepto
Publikováno v:
Acta Epileptologica, Vol 2, Iss 1, Pp 1-6 (2020)
Background Infantile spasms (IS) are the most common childhood epileptic encephalopathy. Focal cortical dysplasia (FCD) and gray matter heterotopias (GH) are common structural causes of IS. The recommended first-line treatment for IS patients with st
Publikováno v:
Cancer Management and Research. 12:769-775
Purpose Glioblastoma multiforme (GBM) is the most common of the malignant and invasive gliomas. High grade glioma is prone to relapse and has a poor prognosis. However, there is a big difference in terms of survival time with the same grade glioma. C
Publikováno v:
Cell Biochemistry and Function. 37:368-376
The growing evidence shows that in the early stage of type 2 diabetes mellitus (T2DM) development, when challenged by hyperglycemia and/or insulin resistance, pancreatic islets would produce more insulin to maintain the balance of blood sugar, but at
Publikováno v:
Future Oncology. 15:1617-1627
Aim: To compare the performance of first-line paclitaxel liposome + oxaliplatin and SOX (tegafur/gimeracil/oteracil + oxaliplatin) in advanced gastric cancer patients. Materials & methods: Stage IIb–IV gastric cancer patients underwent either first
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-6 (2019)
Scientific Reports
Scientific Reports
Hand, foot, and mouth disease (HFMD) is a common childhood infection that causes a substantial disease burden in the Asia-Pacific region. Various climate variables, such as humidity and temperature, have been associated with HFMD. However, few studie
Autor:
Juan Xiong, Fei Yin, Xiaolu Deng, Jing Peng, Li Yang, Lifen Yang, Shimeng Chen, Fang He, Baiyu Chen, Chen Chen, Ciliu Zhang
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 518
Background It has been reported that de novo heterozygous variants of DEAF1 can cause DEAF1-associated neurodevelopmental disorder. The purpose of this article is to explore the clinical and genetic characteristics of Chinese patients harboring de no
Autor:
Zhao Yang, Tung-Yang Cheng, Jin Deng, Zhiyan Wang, Xiaoya Qin, Xi Fang, Yuan Yuan, Hongwei Hao, Yuwu Jiang, Jianxiang Liao, Fei Yin, Yanhui Chen, Liping Zou, Baomin Li, Yuxing Gao, Xiaomei Shu, Shaoping Huang, Feng Gao, Jianmin Liang, Luming Li
Publikováno v:
Frontiers in Neurology
Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology, Vol 12 (2021)
Objective: Intractable epilepsy and uncontrolled seizures could affect cardiac function and the autonomic nerve system with a negative impact on children's growth. The aim of this study was to investigate the variability and complexity of cardiac aut
Autor:
Liwen Wu, Fang He, Ciliu Zhang, Lifen Yang, Fei Yin, Miriam Kessi, Leilei Mao, Jing Peng, Pan Peng
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Scientific Reports
Scientific Reports
Infantile spasms (ISs) is a devastating form of an early infantile epileptic encephalopathy. The patterns of response of multiple regimens, and the difference in response rates for the cases who receive first-line therapies on time versus those who r
Autor:
Fei Yin, Siyi Gan, Ting Xiao, Haiyan Yang, Victor Wei Zhang, Zou Pan, Miriam Kessi, Zhuangyi Yang, Liwen Wu
Publikováno v:
Molecular neurobiology. 57(9)
The aim of this study is to investigate the mitochondrial dysfunction and pathogenic role of the mitochondrial genome in the progression of mesial temporal lobe epilepsy (MTLE) in vivo and in vitro. Mitochondrial DNA (mtDNA) and nuclear DNA were dete