Zhuo-ran Song - Publications

Multifactorial Predictors of Renal Outcomes in Alport Syndrome: Integrating Genetic, Clinical, and Cystic Phenotypes.

Journal: Kidney medicine

Published: March 02, 2026

Dual-hit cystic kidneys: ADPKD with de novo HNF1B deletion.

Journal: Kidney international

Published: August 28, 2025

The authors reply.

Journal: Kidney international

Published: August 20, 2025

Screening for genetic kidney diseases in a dialysis cohort via exome sequencing.

Journal: Clinical kidney journal

Published: August 20, 2025

Autosomal dominant tubulointerstitial kidney disease in Chinese patients.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Published: March 04, 2025

Expanding the spectrum of genetic causes of DNA-specific exonuclease TREX1 variants in thrombotic microangiopathy.

Journal: Kidney international

Published: December 16, 2024

Repeated Kidney Biopsy in Membranoproliferative Glomerulonephritis.

Journal: Kidney diseases (Basel, Switzerland)

Published: November 20, 2024

A Pilot Study on Protective Effect of Ambrisentan on Proteinuria in Patients With Alport Syndrome.

Journal: Kidney international reports

Published: May 29, 2024

Protective Effects of Selective Mineralocorticoid Receptor Antagonist in Alport Syndrome on Top of Renin-Angiotensin-System/ Sodium-Glucose Transporter 2 Blockade.

Journal: Kidney international reports

Published: November 27, 2023

Kidney-Predominant Thrombotic Microangiopathy Associated With TREX1 Frameshift Mutation.

Journal: Kidney international reports

Published: May 26, 2023

ADTKD-UMOD in a girl with a de novo mutation: A case report.

Journal: Frontiers in medicine

Published: October 23, 2022

Efficacy of Dapagliflozin in Adult Autosomal Recessive Alport Syndrome.

Journal: Kidney international reports

Published: June 21, 2022