Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Xin-Hua Bao"'
Autor:
Zhe Zhang, Dan-Hua Zhao, Xu-Tong Zhao, Xiao Zhang, Hui Xiong, Xin-Hua Bao, Yun Yuan, Zhao-Xia Wang, Li-Shao Guo
Publikováno v:
Chinese Medical Journal, Vol 132, Iss 3, Pp 269-274 (2019)
Abstract. Background:. Studies on the relationship between antiepileptic drug (AED) administration and clinical outcomes in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) remain scarce. Levetiracetam
Externí odkaz:
https://doaj.org/article/43e9efecca574ce7bcb5983517ad24c2
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 6, Pp 672-678 (2016)
Background: Wolf-Hirschhorn syndrome (WHS) is a contiguous gene syndrome that is typically caused by a deletion of the distal portion of the short arm of chromosome 4. However, there are few reports about the features of Chinese WHS patients. This st
Externí odkaz:
https://doaj.org/article/ce8259bcf56e4fe5a2bd01d20de55831
Publikováno v:
Applied Mechanics and Materials. :1096-1100
The study on dispersion mechanism of dispersive soil has attracted attention in water conservancy project. In order to investigate the main dispersive influencing factors of soil, grey correlation degree method was used to analysis the relation betwe
Publikováno v:
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences. 47(6)
To demonstrate the clinical manifestation, diagnosis and treatment of myoclonus epilepsy with ragged-red-fibers (MERRF), a case of MERRF was presented with review of the literature. A 4-year-7-month-old girl was diagnosed with MERRF. She had tremor,
Publikováno v:
Solid State Sciences. 8:129-136
In this work, atomic parameters support vector regression (APSVR) was proposed to predict the band gap and melting point of III–V, II–VI binary and I–III–VI2, II–IV–V2 ternary compound semiconductors. The predicted results of APSVR were i
Publikováno v:
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics. 16(7)
To study the relationship between STXBP1 gene mutations and refractory seizures with unknown causes in newborns.The coding region of STXBP1 gene was detected using direct Sanger sequencing in 11 newborns with refractory seizures of unknown causes.STX
Publikováno v:
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences. 46(2)
To analyze the Long-term outcome of seizures, and to explore the effects of related factors, including the age at onset, types of epileptic syndromes, and etiological factors, etc.The clinical data were retrospectively surveyed from 265 children with
Autor:
Yan-yan, Liu, Xin-hua, Bao, Shuang, Wang, Na, Fu, Xiao-yan, Liu, Fu-ying, Song, Yan-ling, Yang, Ye, Wu, Yue-hua, Zhang, Jian-xin, Wu, Yu-wu, Jiang, Jiong, Qin, Xi-ru, Wu
Publikováno v:
Zhonghua er ke za zhi = Chinese journal of pediatrics. 51(6)
To analyze the clinical and SLC2A1 gene mutation characteristics of glucose transporter type 1 deficiency syndrome.The detailed clinical manifestations of six cases were recorded. The laboratory tests including EEG, MRI, blood chemistry, and lumbar p
Publikováno v:
Journal of Amino Acids
Cdc48 (also called VCP and p97) is an abundant protein that plays essential regulatory functions in a broad array of cellular processes. Working with various cofactors, Cdc48 utilizes its ATPase activity to promote the assembly and disassembly of pro
Autor:
Hui, Xiong, Chen-tao, Liu, Yue-hua, Zhang, Xin-hua, Bao, Yu-wu, Jiang, Hong, Zhao, Xiao-ping, Wu, Jiong, Qin
Publikováno v:
Zhonghua er ke za zhi = Chinese journal of pediatrics. 50(12)
Children with refractory epilepsy who suffered from severe liver function impairment during valproic acid (VPA) treatment at routine dosage were studied. The clinical manifestations and therapeutic approaches were investigated in order to improve its