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

par Shao, Leping, Gao, Yanxia, Xu, Yan, Lang, Yanhua
Publié 2012

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

par Zhang, Wei, Xue, Feng, Wang, Cui, Shao, Leping
Publié dans Oncotarget (2017)

Mutation spectrum of Chinese patients with Bartter syndrome

par Han, Yue, Lin, Yi, Sun, Qing, Wang, Shujuan, Gao, Yanxia, Shao, Leping
Publié dans Oncotarget (2017)

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

par Shao, Leping, Cui, Li, Lu, Jingru, Lang, Yanhua, Bottillo, Irene, Zhao, Xiangzhong
Publié dans 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...

par Lu, Jingru, Zhao, Xiangzhong, Paiardini, Alessandro, Lang, Yanhua, Bottillo, Irene, Shao, Leping
Publié dans BMC Nephrol (2018)

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

par Zhao, Xiangzhong, Lu, Jingru, Gao, Yanxia, Wang, Xiaoling, Lang, Yanhua, Shao, Leping
Publié dans BMC Nephrol (2018)

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

par Wang, Cui, Lu, Jingru, Lang, Yanhua, Liu, Ting, Wang, Xiaoling, Zhao, Xiangzhong, Shao, Leping
Publié dans Sci Rep (2016)

Stromal proteome expression profile and muscle-invasive bladder cancer research

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

Stromal proteome expression profile and muscle-invasive bladder cancer research

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

par Zhang, Ruixiao, Wang, Jianhong, Wang, Qing, Han, Yue, Liu, Xuejun, Bottillo, Irene, Lang, Yanhua, Shao, Leping
Publié dans BMC Med Genet (2018)

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

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

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

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

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

par 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
Publié dans Ren Fail (2020)