Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anshuo Wang"'
Autor:
Xueting Cheng, Jiahuan Chen, Xueying Yang, Han Chan, Xia Yang, Jia Jiao, Anshuo Wang, Gaofu Zhang, Xuelan Chen, Xiaoqin Li, Mo Wang, Baohui Yang, Haiping Yang, Qiu Li
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-14 (2024)
Abstract Background Steroid-resistant nephrotic syndrome (SRNS) are monogenic in some cases, however, there are still no clear guidelines on genetic testing in the clinical practice of SRNS in children. Methods Three hundred thirty-two children were
Externí odkaz:
https://doaj.org/article/cbc3ec2642694ae9a825d410c3f22e4f
Autor:
Qilin Chen, Huimin Jiang, Rong Ding, Jinjie Zhong, Longfei Li, Junli Wan, Xiaoqian Feng, Liping Peng, Xia Yang, Han Chen, Anshuo Wang, Jia Jiao, Qin Yang, Xuelan Chen, Xiaoqin Li, Lin Shi, Gaofu Zhang, Mo Wang, Haiping Yang, Qiu Li
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Nephrotic syndrome (NS) is a relatively rare and serious presentation of IgA nephropathy (IgAN) (NS-IgAN). Previous research has suggested that the pathogenesis of NS-IgAN may involve circulating immune imbalance and kidney injury; however, this has
Externí odkaz:
https://doaj.org/article/d5503b70c6594198a04226abbd6a8428
Autor:
Jia Jiao, Li Wang, Fenfen Ni, Mo Wang, Shipin Feng, Xiaojie Gao, Han Chan, Xueying Yang, Hao Lee, Huan Chi, Xuelan Chen, Daoqi Wu, Gaofu Zhang, Baohui Yang, Anshuo Wang, Qin Yang, Junli Wan, Sijie Yu, Xiaoqin Li, Mei Wang, Xiaofeng Chen, Xianying Mai, Xiongzhong Ruan, Haiping Yang, Qiu Li
Publikováno v:
Genes and Diseases, Vol 9, Iss 6, Pp 1662-1673 (2022)
Understanding the association between the genetic and clinical phenotypes in children with nephrotic syndrome (NS) of different etiologies is critical for early clinical guidance. We employed whole-exome sequencing (WES) to detect monogenic causes of
Externí odkaz:
https://doaj.org/article/3a664aabdee94df8a9a50673eaa071a6
Autor:
Rui Liang, Xuelan Chen, Ying Zhang, Chak-Fun Law, Sijie Yu, Jia Jiao, Qin Yang, Daoqi Wu, Gaofu Zhang, Han Chen, Mo Wang, Haiping Yang, Anshuo Wang
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Externí odkaz:
https://doaj.org/article/d46b55f4cdf74c89bac6f7df53401fa6
Autor:
Rui Liang, Xuelan Chen, Ying Zhang, Chak-Fun Law, Sijie Yu, Jia Jiao, Qin Yang, Daoqi Wu, Gaofu Zhang, Han Chen, Mo Wang, Haiping Yang, Anshuo Wang
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2023)
ObjectiveCOQ8B nephropathy is a relatively rare autosomal recessive kidney disease characterized by proteinuria and a progressive deterioration of renal function, eventually leading to end-stage renal disease (ESRD). The objective is to study the cha
Externí odkaz:
https://doaj.org/article/93ca46fbb4e443929fd5c2cae7605ef3
Publikováno v:
Journal of Craniofacial Surgery; Jun2024, Vol. 35 Issue 4, p1181-1185, 5p
Autor:
Qilin Chen, Huimin Jiang, Rong Ding, Jinjie Zhong, Longfei Li, Junli Wan, Xiaoqian Feng, Liping Peng, Xia Yang, Han Chen, Anshuo Wang Wang, Jia Jiao, Qin Yang, Xuelan Chen, Xiaoqin Li, Lin Shi, Gaofu Zhang, Mo Wang, Qiu Li, Haiping Yang
Publikováno v:
SSRN Electronic Journal.