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

بواسطة Shao, Leping, Gao, Yanxia, Xu, Yan, Lang, Yanhua
منشور في 2012

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

بواسطة Zhang, Wei, Xue, Feng, Wang, Cui, Shao, Leping
الحاوية / القاعدة Oncotarget (2017)

Mutation spectrum of Chinese patients with Bartter syndrome

بواسطة Han, Yue, Lin, Yi, Sun, Qing, Wang, Shujuan, Gao, Yanxia, Shao, Leping
الحاوية / القاعدة Oncotarget (2017)

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

بواسطة Shao, Leping, Cui, Li, Lu, Jingru, Lang, Yanhua, Bottillo, Irene, Zhao, Xiangzhong
الحاوية / القاعدة 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...

بواسطة Lu, Jingru, Zhao, Xiangzhong, Paiardini, Alessandro, Lang, Yanhua, Bottillo, Irene, Shao, Leping
الحاوية / القاعدة BMC Nephrol (2018)

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

بواسطة Zhao, Xiangzhong, Lu, Jingru, Gao, Yanxia, Wang, Xiaoling, Lang, Yanhua, Shao, Leping
الحاوية / القاعدة BMC Nephrol (2018)

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

بواسطة Wang, Cui, Lu, Jingru, Lang, Yanhua, Liu, Ting, Wang, Xiaoling, Zhao, Xiangzhong, Shao, Leping
الحاوية / القاعدة Sci Rep (2016)

Stromal proteome expression profile and muscle-invasive bladder cancer research

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

Stromal proteome expression profile and muscle-invasive bladder cancer research

بواسطة Niu, Haitao, Jiang, Haiping, Cheng, Bo, Li, Xinhui, Dong, Qian, Shao, Leping, Liu, Shiguo, Wang, Xinsheng
منشور في 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

بواسطة Zhang, Ruixiao, Wang, Jianhong, Wang, Qing, Han, Yue, Liu, Xuejun, Bottillo, Irene, Lang, Yanhua, Shao, Leping
الحاوية / القاعدة BMC Med Genet (2018)

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

بواسطة Wang, Sai, Wang, Yixiu, Wang, Jinchao, Liu, Zhiying, Zhang, Ruixiao, Shi, Xiaomeng, Han, Yue, Guo, Wencong, Bottillo, Irene, Shao, Leping
الحاوية / القاعدة Front Genet (2020)

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

بواسطة Zhao, Xiangzhong, Cui, Li, Lang, Yanhua, liu, Ting, Lu, Jingru, Wang, Cui, Tuffery-Giraud, Sylvie, Bottillo, Irene, Wang, Xinsheng, Shao, Leping
الحاوية / القاعدة Sci Rep (2016)

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

بواسطة 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
الحاوية / القاعدة Ren Fail (2020)