Percutaneous Transluminal Revascularization following an Angiotensin Receptor Blocker: Successful Treatment for Flash Pulmonary Edema and Hyponatremic Hypertensive Syndrome

Por Shao, Leping, Gao, Yanxia, Xu, Yan, Lang, Yanhua
Publicado em 2012

Clinical features and prognostic factors of ten patients with renal failure caused by IgG4-related retroperitoneal fibrosis

Por Zhang, Wei, Xue, Feng, Wang, Cui, Shao, Leping
Publicado no Oncotarget (2017)

Mutation spectrum of Chinese patients with Bartter syndrome

Por Han, Yue, Lin, Yi, Sun, Qing, Wang, Shujuan, Gao, Yanxia, Shao, Leping
Publicado no Oncotarget (2017)

A novel mutation in exon 9 of Cullin 3 gene contributes to aberrant splicing in pseudohypoaldosteronism type II

Por Shao, Leping, Cui, Li, Lu, Jingru, Lang, Yanhua, Bottillo, Irene, Zhao, Xiangzhong
Publicado no FEBS Open Bio (2018)

Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a...

Por Lu, Jingru, Zhao, Xiangzhong, Paiardini, Alessandro, Lang, Yanhua, Bottillo, Irene, Shao, Leping
Publicado no BMC Nephrol (2018)

Novel compound heterozygous ATP6V1B1 mutations in a Chinese child patient with primary distal renal tubular acidosis: a case report

Por Zhao, Xiangzhong, Lu, Jingru, Gao, Yanxia, Wang, Xiaoling, Lang, Yanhua, Shao, Leping
Publicado no BMC Nephrol (2018)

Two novel AGXT mutations identified in primary hyperoxaluria type-1 and distinct morphological and structural difference in kidney stones

Por Wang, Cui, Lu, Jingru, Lang, Yanhua, Liu, Ting, Wang, Xiaoling, Zhao, Xiangzhong, Shao, Leping
Publicado no Sci Rep (2016)

Stromal proteome expression profile and muscle-invasive bladder cancer research

Por Niu Haitao, Jiang Haiping, Cheng Bo, Li Xinhui, Dong Qian, Shao Leping, Liu Shiguo, Wang Xinsheng
Publicado em 2012-08-01

Stromal proteome expression profile and muscle-invasive bladder cancer research

Por Niu, Haitao, Jiang, Haiping, Cheng, Bo, Li, Xinhui, Dong, Qian, Shao, Leping, Liu, Shiguo, Wang, Xinsheng
Publicado em 2012

Identification of a novel TSC2 c.3610G > A, p.G1204R mutation contribute to aberrant splicing in a patient with classical tuberous sclerosis complex: a case report

Por Zhang, Ruixiao, Wang, Jianhong, Wang, Qing, Han, Yue, Liu, Xuejun, Bottillo, Irene, Lang, Yanhua, Shao, Leping
Publicado no BMC Med Genet (2018)

Six Exonic Variants in the SLC5A2 Gene Cause Exon Skipping in a Minigene Assay

Por Wang, Sai, Wang, Yixiu, Wang, Jinchao, Liu, Zhiying, Zhang, Ruixiao, Shi, Xiaomeng, Han, Yue, Guo, Wencong, Bottillo, Irene, Shao, Leping
Publicado no Front Genet (2020)

A recurrent deletion in the SLC5A2 gene including the intron 7 branch site responsible for familial renal glucosuria

Por Zhao, Xiangzhong, Cui, Li, Lang, Yanhua, liu, Ting, Lu, Jingru, Wang, Cui, Tuffery-Giraud, Sylvie, Bottillo, Irene, Wang, Xinsheng, Shao, Leping
Publicado no Sci Rep (2016)

Sudden onset of nephrotic syndrome in an asymptomatic Fabry patient: a case report

Por Zhang, Ruixiao, Chen, Zeqing, Lang, Yanhua, Shao, Shihong, Cai, Yan, You, Qingqing, Sun, Yan, Wang, Sai, Shi, Xiaomeng, Liu, Zhiying, Guo, Wencong, Han, Yue, Shao, Leping
Publicado no Ren Fail (2020)