Zihua Yu

发表

Effects of alternative remission criteria on outcome of pediatric proliferative lupus nephritis: a multi-center retrospective study of pediatric proliferative lupus nephritis.

Cheng Cheng, Wei Chen, Jun Huang, 2021, American journal of translational research.

A child with painful swollen joints, rash and proteinuria: Answers

X. Nie, Zihua Yu, Chengdong Kang, 2020, Pediatric Nephrology.

WT1 Gene Mutations in Chinese Children With Early Onset Nephrotic Syndrome

Dan-hua Zhao, Jie Ding, Hongwen Zhang, 2010, Pediatric Research.

R168H and V165X mutant podocin might induce different degrees of podocyte injury via different molecular mechanisms

Jie Ding, Jing Miao, Q. Fan, 2009, Genes to cells : devoted to molecular & cellular mechanisms.

Mutations in NUP160 Are Implicated in Steroid-Resistant Nephrotic Syndrome.

N. Chen, Zhe Han, X. Nie, 2019, Journal of the American Society of Nephrology : JASN.

Mutations in NPHS2 in sporadic steroid-resistant nephrotic syndrome in Chinese children.

Jie Ding, Jing-cheng Liu, Zihua Yu, 2005, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Knockdown of NUP160 inhibits cell proliferation, induces apoptosis, autophagy and cell migration, and alters the expression and localization of podocyte associated molecules in mouse podocytes.

X. Nie, Ping Wang, Zihua Yu, 2018, Gene.

A child with isolated nephrotic syndrome and WT1 mutation presenting as a 46, XY phenotypic male

X. Nie, Jun Huang, Zihua Yu, 2012, European Journal of Pediatrics.

The Clinical and Genetic Features in Chinese Children With Steroid-Resistant or Early-Onset Nephrotic Syndrome: A Multicenter Cohort Study

Jie Ding, Yanqin Zhang, Qing Yang, 2022, Frontiers in Medicine.

Growth hormone treatment in pre-pubertal short Chinese children with chronic kidney disease prior to transplantation

Jianhua Mao, Zhi Chen, Jun Huang, 2022, Pediatric Research.

Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome

Jie Ding, Hongwen Zhang, Yanqin Zhang, 2017, Pediatric Nephrology.

Genetic variations of the NR3C1 gene in children with sporadic nephrotic syndrome.

Jie Ding, Ying Shen, Zihua Yu, 2006, Biochemical and biophysical research communications.

A novel mutation of NPHS2 identified in a Chinese family

Jie Ding, N. Guan, Yan Shi, 2004, Pediatric Nephrology.

Long‐term nephrotic syndrome recurrence risk of kidney transplantation in two siblings with ADCK4‐associated glomerulopathy

Zihua Yu, F. Zhao, Sihua Wang, 2021, Pediatric transplantation.

Early plasma exchange for treating ricin toxicity in children after castor bean ingestion

X. Nie, Guang-ming Chen, Cheng-feng Wang, 2015, Journal of clinical apheresis.

Rethinking genotype-phenotype correlations in papillorenal syndrome: a case report on an unusual congenital camptodactyly and skeletal deformity with a heterogeneous PAX2 mutation of hexanucleotide duplication.

Ping Wang, Zihua Yu, Juan Huang, 2018, Gene.

Early plasma exchange for treating ricin toxicity in children after castor bean ingestion

X. Nie, Guang-ming Chen, Cheng-feng Wang, 2015, Journal of clinical apheresis.

Clinicopathologic features in childhood-onset lupus nephritis with antineutrophil cytoplasmic antibody positivity——a multi-center retrospective study

Jun Huang, Xiaoyun Jiang, Lizhi Chen, 2023, Lupus.