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

Yazar: Shao, Leping, Gao, Yanxia, Xu, Yan, Lang, Yanhua
Baskı/Yayın Bilgisi 2012

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

Yazar: Zhang, Wei, Xue, Feng, Wang, Cui, Shao, Leping
Yayımlandı Oncotarget (2017)

Mutation spectrum of Chinese patients with Bartter syndrome

Yazar: Han, Yue, Lin, Yi, Sun, Qing, Wang, Shujuan, Gao, Yanxia, Shao, Leping
Yayımlandı Oncotarget (2017)

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

Yazar: Shao, Leping, Cui, Li, Lu, Jingru, Lang, Yanhua, Bottillo, Irene, Zhao, Xiangzhong
Yayımlandı 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...

Yazar: Lu, Jingru, Zhao, Xiangzhong, Paiardini, Alessandro, Lang, Yanhua, Bottillo, Irene, Shao, Leping
Yayımlandı BMC Nephrol (2018)

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

Yazar: Zhao, Xiangzhong, Lu, Jingru, Gao, Yanxia, Wang, Xiaoling, Lang, Yanhua, Shao, Leping
Yayımlandı BMC Nephrol (2018)

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

Yazar: Wang, Cui, Lu, Jingru, Lang, Yanhua, Liu, Ting, Wang, Xiaoling, Zhao, Xiangzhong, Shao, Leping
Yayımlandı Sci Rep (2016)

Stromal proteome expression profile and muscle-invasive bladder cancer research

Yazar: Niu Haitao, Jiang Haiping, Cheng Bo, Li Xinhui, Dong Qian, Shao Leping, Liu Shiguo, Wang Xinsheng
Baskı/Yayın Bilgisi 2012-08-01

Stromal proteome expression profile and muscle-invasive bladder cancer research

Yazar: Niu, Haitao, Jiang, Haiping, Cheng, Bo, Li, Xinhui, Dong, Qian, Shao, Leping, Liu, Shiguo, Wang, Xinsheng
Baskı/Yayın Bilgisi 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

Yazar: Zhang, Ruixiao, Wang, Jianhong, Wang, Qing, Han, Yue, Liu, Xuejun, Bottillo, Irene, Lang, Yanhua, Shao, Leping
Yayımlandı BMC Med Genet (2018)

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

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

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

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

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

Yazar: 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
Yayımlandı Ren Fail (2020)