Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Zhaoshi Yi"'
Autor:
Xingying Zeng, Yong Chen, Xiongying Yu, Yuanyuan Che, Hui Chen, Zhaoshi Yi, Jie Qin, Jianmin Zhong
Publikováno v:
Acta Epileptologica, Vol 5, Iss 1, Pp 1-8 (2023)
Abstract Background SYNGAP1 is a significant genetic risk factor for global developmental delay, autism spectrum disorder, and epileptic encephalopathy. De novo loss-of-function variants in this gene cause a neurodevelopmental disorder, for example,
Externí odkaz:
https://doaj.org/article/8d90dc4ce1194d3aa8b2c6d111d3a7ed
Publikováno v:
Acta Epileptologica, Vol 4, Iss 1, Pp 1-7 (2022)
Abstract Background To realize the clinical characteristics of long QT syndrome (LQTS) caused by antiseizure medicines (ASMs), and to improve the prevention and management of ASM-acquired QT syndrome. Case presentation A case of ASM-acquired QT syndr
Externí odkaz:
https://doaj.org/article/dd04a388761a417898673c5cff1a2dd5
Autor:
Xiaoyan Li, Zhixin Huang, Yong Chen, Xiaolan Sun, Zhaoshi Yi, Jihua Xie, Xiongying Yu, Hui Chen, Jianmin Zhong
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-6 (2022)
Abstract Background Thiamine metabolism dysfunction syndrome 5 (THMD5) is a rare inherited metabolic disorder due to thiamine pyrophosphokinase 1(TPK1) deficiency, caused by mutations in TPK1. The core symptoms of the disease is acute or subacute ons
Externí odkaz:
https://doaj.org/article/ee951706fe034d26b441469169dbf7d3
Autor:
Hui Chen, Xiaolan Sun, Ruiyan Wang, Zhaoshi Yi, Zhixin Huang, Jihua Xie, Xiongying Yu, Yong Chen, Jianmin Zhong
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background Hemiplegic migraine (HM) is an uncommon subtype of migraine with aura including motor weakness. The core symptoms of HM are headache and motor weakness. However, we report a rare case of atypical HM with nonheadache onset in a Chi
Externí odkaz:
https://doaj.org/article/64667475412542feb356e5363b435ae7
Autor:
Xiaoyan Li, Hua Xie, Qian Chen, Xiongying Yu, Zhaoshi Yi, Erzhen Li, Ting Zhang, Jian Wang, Jianmin Zhong, Xiaoli Chen
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-10 (2017)
Abstract Background Chromosomal duplication at the Xq28 region including the MECP2 gene, share consistent clinical phenotypes and a distinct facial phenotype known as MECP2 duplication syndrome. The typical clinical features include infantile hypoton
Externí odkaz:
https://doaj.org/article/ab72fa38b98e44f3a6d98e5450e3efd1
Publikováno v:
MedicineReference. 101(50)
previous studies have shown that phenobarbital (PB) is a effective and safe drug in the treatment of benign convulsions with mild gastroenteritis (CwG), but there is a lack of large sample prospective randomized controlled study of different doses. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba39059cb7b5f48aa3df8b9dbf854e72
https://pubmed.ncbi.nlm.nih.gov/36550836
https://pubmed.ncbi.nlm.nih.gov/36550836
Autor:
Jihua Xie, Yong Chen, Jianmin Zhong, Xiaolan Sun, Zhixin Huang, Ruiyan Wang, Xiongying Yu, Zhaoshi Yi, Hui Chen
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-6 (2021)
BMC Neurology
BMC Neurology
Background Hemiplegic migraine (HM) is an uncommon subtype of migraine with aura including motor weakness. The core symptoms of HM are headache and motor weakness. However, we report a rare case of atypical HM with nonheadache onset in a Chinese chil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fd72106cc626c704b15f2fafeb6c899
https://doaj.org/article/64667475412542feb356e5363b435ae7
https://doaj.org/article/64667475412542feb356e5363b435ae7
Publikováno v:
Seizure. 71:174-178
Purpose To compare the clinical efficacy of high-dose prednisone monotherapy and the combination of hormone and moderate-dose topiramate (TPM) therapy in children with infantile spasms (IS) and late-onset epileptic spasms (ES), and to evaluate whethe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::253deb8dae87e4786b1db92e443e29f4
https://doi.org/10.1016/j.seizure.2019.07.016
https://doi.org/10.1016/j.seizure.2019.07.016
Autor:
Yong Chen, Xiaoyan Li, Huaping Wu, Zhaoshi Yi, Hui Chen, Jianmin Zhong, Yu Yang, Xiongying Yu
Publikováno v:
Diagnostic Microbiology and Infectious Disease. 100:115180
Balamuthia mandrillaris encephalitis is a rare disease with high mortality in the children. Due to the lack of specificity in clinical manifestations, laboratory tests, and neuroimaging, the diagnosis of the disease is difficult, especially the diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32960f3653c546848210642fed678875
https://doi.org/10.1016/j.diagmicrobio.2020.115180
https://doi.org/10.1016/j.diagmicrobio.2020.115180
Publikováno v:
Brain and Development. 37:23-28
Objectives: The aim of this study is to preliminarily evaluate the clinical efficacy and safety of high-dose prednisone in the treatment of infantile spasms (IS) in China, and to provide additional choice of the therapy of IS. Methods: Twenty patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::623d81a1d88cbbb06c195ed647c551cc
https://doi.org/10.1016/j.braindev.2014.02.005
https://doi.org/10.1016/j.braindev.2014.02.005