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

di Shao, Leping, Gao, Yanxia, Xu, Yan, Lang, Yanhua
Pubblicazione 2012

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

di Zhang, Wei, Xue, Feng, Wang, Cui, Shao, Leping
Pubblicato in Oncotarget (2017)

Mutation spectrum of Chinese patients with Bartter syndrome

di Han, Yue, Lin, Yi, Sun, Qing, Wang, Shujuan, Gao, Yanxia, Shao, Leping
Pubblicato in Oncotarget (2017)

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

di Shao, Leping, Cui, Li, Lu, Jingru, Lang, Yanhua, Bottillo, Irene, Zhao, Xiangzhong
Pubblicato in 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...

di Lu, Jingru, Zhao, Xiangzhong, Paiardini, Alessandro, Lang, Yanhua, Bottillo, Irene, Shao, Leping
Pubblicato in BMC Nephrol (2018)

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

di Zhao, Xiangzhong, Lu, Jingru, Gao, Yanxia, Wang, Xiaoling, Lang, Yanhua, Shao, Leping
Pubblicato in BMC Nephrol (2018)

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

di Wang, Cui, Lu, Jingru, Lang, Yanhua, Liu, Ting, Wang, Xiaoling, Zhao, Xiangzhong, Shao, Leping
Pubblicato in Sci Rep (2016)

Stromal proteome expression profile and muscle-invasive bladder cancer research

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

Stromal proteome expression profile and muscle-invasive bladder cancer research

di Niu, Haitao, Jiang, Haiping, Cheng, Bo, Li, Xinhui, Dong, Qian, Shao, Leping, Liu, Shiguo, Wang, Xinsheng
Pubblicazione 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

di Zhang, Ruixiao, Wang, Jianhong, Wang, Qing, Han, Yue, Liu, Xuejun, Bottillo, Irene, Lang, Yanhua, Shao, Leping
Pubblicato in BMC Med Genet (2018)

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

di Wang, Sai, Wang, Yixiu, Wang, Jinchao, Liu, Zhiying, Zhang, Ruixiao, Shi, Xiaomeng, Han, Yue, Guo, Wencong, Bottillo, Irene, Shao, Leping
Pubblicato in Front Genet (2020)

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

di Zhao, Xiangzhong, Cui, Li, Lang, Yanhua, liu, Ting, Lu, Jingru, Wang, Cui, Tuffery-Giraud, Sylvie, Bottillo, Irene, Wang, Xinsheng, Shao, Leping
Pubblicato in Sci Rep (2016)

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

di 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
Pubblicato in Ren Fail (2020)