Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Chengqing Yang"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-9 (2024)
Abstract Background Pitt–Hopkins syndrome (PTHS) is a rare genetic condition caused by a mutation in the transcription Factor 4 (TCF4) gene and characterized by its unique clinical presentations. At present, there is an incomplete understanding of
Externí odkaz:
https://doaj.org/article/50ecf746ab9644b0b23689739381b812
Autor:
Jiao Xue, Zhenfeng Song, Hongshan Zhao, Zhi Yi, Fei Li, Chengqing Yang, Kaixuan Liu, Ying Zhang
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-7 (2024)
Abstract Background Acute bulbar palsy-plus (ABPp) syndrome is an unusual variant of Guillain-Barré syndrome (GBS). Anti-GT1a and anti-GQ1b antibodies have been reported in patients with ABPp, but without reports related to GD3 antibodies. Methods C
Externí odkaz:
https://doaj.org/article/9ecc2bbaf131407f986e50e010932571
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
The possible protective effect of interleukin-32 (IL-32) in Mycobacterium tuberculosis (Mtb) infection has been indicated. However, few studies have been focused on IL-32 in tuberculosis patients. Additionally, the regulation of IL-32 production has
Externí odkaz:
https://doaj.org/article/282ec0bc016648359980adefae1c82a7
Autor:
Zhi Yi, Zhenfeng Song, Jiao Xue, Chengqing Yang, Fei Li, Hua Pan, Xuan Feng, Ying Zhang, Hong Pan
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-9 (2022)
Abstract Background Developmental and epileptic encephalopathies (DEEs) are a heterogeneous group of severe disorders that are characterized by early-onset, refractory seizures and developmental slowing or regression. Genetic variations are significa
Externí odkaz:
https://doaj.org/article/5427daa4586944bfa29d93ccec10de68
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionHemiplegic migraine (HM) is a rare subtype of migraine. HM in children may be atypical in the initial stage of the disease, which could easily lead to misdiagnosis.MethodsWe report two cases of atypical hemiplegic migraine that onset as a
Externí odkaz:
https://doaj.org/article/7aec439d69c449528b67f815b41dd4e9
Publikováno v:
Journal of Clinical Tuberculosis and Other Mycobacterial Diseases, Vol 31, Iss , Pp 100355- (2023)
Background: Tuberculosis (TB) continues to be a common disease in developing countries, among which middle ear TB is rare. Furthermore, it is relatively difficult to make an early diagnosis and provide follow-up treatment for middle ear TB. So, it is
Externí odkaz:
https://doaj.org/article/3c3555b0515d451b8258d963b8b8a668
Autor:
Jiao Xue, Chongfeng Duan, Guizhi Xu, Ying Zhang, Zhenfeng Song, Zhi Yi, Chengqing Yang, Fei Li, Kaixuan Liu, Hongshan Zhao, Xuejun Liu
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-6 (2022)
Abstract Background Mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) has been reported worldwidely. However, the data about recurrent cases is limited. We aimed to analyze the clinical and radiographic features of recurrent M
Externí odkaz:
https://doaj.org/article/55f9264fc30a4605b953b5763c70330f
Autor:
Qiping Ge, Yan Ma, Lijie Zhang, Liping Ma, Caiyan Zhao, Yuhui Chen, Xuerui Huang, Wei Shu, Shengyu Chen, Fei Wang, Bo Li, Xiqin Han, Lian Shi, Xin Wang, Youlun Li, Shangpeng Yang, Wenli Cao, Qianying Liu, Ling Chen, Chao Wu, Bing Ouyang, Furong Wang, Po Li, Xiang Wu, Xiue Xi, Xueyan Leng, Haiqing Zhang, Hua Li, Juan Li, Chengqing Yang, Peng Zhang, Hongzhe Cui, Yuhong Liu, Chengcheng Kong, Zhaogang Sun, Jian Du, Weiwei Gao
Publikováno v:
Frontiers in Public Health, Vol 11 (2023)
Background and objectiveRetreatment pulmonary tuberculosis (PTB) still accounts for a large proportion of tuberculosis, and the treatment outcome is unfavorable. The recurrence of retreatment PTB based on long-term follow-up has not been well demonst
Externí odkaz:
https://doaj.org/article/3453658518a64387a077a431bf8f1e7c
Autor:
Jie Song, Yedan Liu, Ya Guo, Zhenghai Qu, Peipei Liu, Fei Li, Chengqing Yang, Fan Fan, Zongbo Chen
Publikováno v:
Immunity, Inflammation and Disease, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract Introduction This study was designed to explore the association between the TMEM173 polymorphism (rs7447927) and the severity of enterovirus 71 (EV71) infection among Chinese children. Methods The TMEM173 polymorphism was identified in EV71
Externí odkaz:
https://doaj.org/article/4706e0415fb44d3fa043c53177321a09
Autor:
Jie Song, Yedan Liu, Ya Guo, Peipei Liu, Fei Li, Chengqing Yang, Xiaoyu Pan, Liping Yi, Fan Fan, Han Zhao, Zongbo Chen
Publikováno v:
Immunity, Inflammation and Disease, Vol 10, Iss 5, Pp n/a-n/a (2022)
Abstract Introduction This study aimed to explore the association between the IRAK4 polymorphism rs4251545 and the severity of enterovirus 71 (EV71) infection in Chinese children. Methods We analyzed the IRAK4 polymorphism rs4251545 in 617 EV71‐inf
Externí odkaz:
https://doaj.org/article/d6730f54731c4699abd6ed9cf06de1c3