Zhenle Yang

324 Jingwu Road
Jinan, China

Last Updated: 09/26/2026

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Found 14 publications

Identification of IL7R as a key genetic risk locus in childhood steroid-sensitive nephrotic syndrome and IgA nephropathy.

Identification of IL7R as a key genetic risk locus in childhood steroid-sensitive nephrotic syndrome and IgA nephropathy.

Journal: Frontiers in immunology

Published: February 08, 2026

An unusual trilogy: a case of comorbid aHUS, Fabry disease, and hypertrophic cardiomyopathy.

An unusual trilogy: a case of comorbid aHUS, Fabry disease, and hypertrophic cardiomyopathy.

Journal: Frontiers in medicine

Published: September 07, 2025

Polygenic risk score from steroid-sensitive nephrotic syndrome GWAS indicates overlapping genetic basis with steroid-resistant cases.

Polygenic risk score from steroid-sensitive nephrotic syndrome GWAS indicates overlapping genetic basis with steroid-resistant cases.

Journal: Scientific reports

Published: August 16, 2025

Mycophenolate Mofetil versus Cyclophosphamide for Initial Therapy in Childhood-Onset Proliferative Lupus Nephritis: A Prospective, Multicenter, Randomized Trial.

Mycophenolate Mofetil versus Cyclophosphamide for Initial Therapy in Childhood-Onset Proliferative Lupus Nephritis: A Prospective, Multicenter, Randomized Trial.

Journal: Journal of the American Society of Nephrology : JASN

Published: January 24, 2025

Treatment of thrombotic microangiopathy associated with systemic lupus erythematosus with low-dose rituximab as an induction agent and belimumab as a maintenance agent.

Treatment of thrombotic microangiopathy associated with systemic lupus erythematosus with low-dose rituximab as an induction agent and belimumab as a maintenance agent.

Journal: BMC pediatrics

Published: October 08, 2024

Clinical features and genetic analysis of 15 Chinese children with dent disease.

Clinical features and genetic analysis of 15 Chinese children with dent disease.

Journal: Renal failure

Published: May 10, 2024

Systemic lupus erythematosus combined with Wilson's disease: a case report and literature review.

Systemic lupus erythematosus combined with Wilson's disease: a case report and literature review.

Journal: BMC pediatrics

Published: November 18, 2023

Congenital chloride diarrhoea in a Chinese infant with a compound heterozygous SLC26A3 mutation.

Congenital chloride diarrhoea in a Chinese infant with a compound heterozygous SLC26A3 mutation.

Journal: BMC pediatrics

Published: October 23, 2023

Umbelliferone attenuates cisplatin-induced acute kidney injury by inhibiting oxidative stress and inflammation via NRF2.

Umbelliferone attenuates cisplatin-induced acute kidney injury by inhibiting oxidative stress and inflammation via NRF2.

Journal: Physiological reports

Published: July 11, 2023

A novel mutation of the RPGRIP1L gene in a Chinese boy with Joubert syndrome with oculorenal involvement.

A novel mutation of the RPGRIP1L gene in a Chinese boy with Joubert syndrome with oculorenal involvement.

Journal: BMC pediatrics

Published: February 03, 2023

Low molecular weight proteinuria, congenital myopia and hearing loss in a 10-year-old boy: Questions.

Low molecular weight proteinuria, congenital myopia and hearing loss in a 10-year-old boy: Questions.

Journal: Pediatric nephrology (Berlin, Germany)

Published: November 22, 2022

Low molecular weight proteinuria, congenital myopia and hearing loss in a 10-year-old boy: Answers.

Low molecular weight proteinuria, congenital myopia and hearing loss in a 10-year-old boy: Answers.

Journal: Pediatric nephrology (Berlin, Germany)

Published: November 22, 2022

Showing 1-12 of 14

Last Updated: 09/26/2026