Suchergebnisse - "Zhuang, Jieqiu"

PubPharm (30)

1

Urine Screening and 9 Years' Medical Record System Follow-Up Among School Students in Wenzhou, China

enthalten in: Frontiers in pediatrics | 2022

von Chen, T. | Yang, Q. | Xu, H. | +8

2

Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort

enthalten in: BMC medical genomics | 2021

von Yang, X. | Li, Y. | Fang, Y. | +26

3

Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort

enthalten in: BMC medical genomics | 2021

von Yang, X. | Li, Y. | Fang, Y. | +26

4

The important roles and molecular mechanisms of annexin A2 autoantibody in children with nephrotic syndrome

enthalten in: Annals of translational medicine | 2021

von Ye, Q. | Zhang, Y. | Zhuang, J. | +22

ErratumIn: Ann Transl Med. 2023 Oct 25;11(11):401. - PMID 37970603

5

Genetic Architecture of Childhood Kidney and Urological Diseases in China

enthalten in: Phenomics (Cham, Switzerland) | 2021

von Fang, Y. | Shi, H. | Xiang, T. | +66

6

Genetic Architecture of Childhood Kidney and Urological Diseases in China

enthalten in: Phenomics | 2021

von Fang, Y. | Shi, H. | Xiang, T. | +66

7

Genetic Architecture of Childhood Kidney and Urological Diseases in China

enthalten in: Phenomics | 2021

von Fang, Y. | Shi, H. | Xiang, T. | +66

8

Genetic Architecture of Childhood Kidney and Urological Diseases in China

enthalten in: Phenomics | 2021

von Fang, Y. | Shi, H. | Xiang, T. | +66

9

Multi-centre study of the clinical features and gene variant spectrum of Gitelman syndrome in Chinese children

enthalten in: Clinical genetics | 2021

von Shen, Q. | Chen, J. | Yu, M. | +16

10

Multi‐centre study of the clinical features and gene variant spectrum of Gitelman syndrome in Chinese children

enthalten in: Clinical Genetics | 2021

von Shen, Q. | Chen, J. | Yu, M. | +15