Ruochen Che

72 Guangzhou Road
Nanjing, 210008, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 22 publications

A causal link or coincidence? Anti-nephrin antibody-positive minimal change disease coexisting with neuroblastoma in a child.

A causal link or coincidence? Anti-nephrin antibody-positive minimal change disease coexisting with neuroblastoma in a child.

Journal: BMC nephrology

Published: January 07, 2026

Challenges of pediatric ectopic ACTH syndrome from sacrococcygeal teratoma.

Challenges of pediatric ectopic ACTH syndrome from sacrococcygeal teratoma.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: September 30, 2025

Unprecedented coexistence of Dent's disease type 1 and Wilson's disease in a two-year-old Chinese boy: implications for precision medicine.

Unprecedented coexistence of Dent's disease type 1 and Wilson's disease in a two-year-old Chinese boy: implications for precision medicine.

Journal: BMC nephrology

Published: September 05, 2025

18 F-FDG PET/CT and 68 Ga-DOTA-NOC PET/MRI in an Adolescent With Ectopic Adrenocorticotropic Hormone Syndrome From a Presacral Teratoma.

18 F-FDG PET/CT and 68 Ga-DOTA-NOC PET/MRI in an Adolescent With Ectopic Adrenocorticotropic Hormone Syndrome From a Presacral Teratoma.

Journal: Clinical nuclear medicine

Published: August 11, 2025

Phenotype and genotype analyses of 21 Chinese patients with Dent disease.

Phenotype and genotype analyses of 21 Chinese patients with Dent disease.

Journal: Journal of biomedical research

Published: May 27, 2025

Functional analysis of heterozygous variants in the SALL1 gene in 2 children with Townes-Brocks syndrome with FSGS.

Functional analysis of heterozygous variants in the SALL1 gene in 2 children with Townes-Brocks syndrome with FSGS.

Journal: BMC pediatrics

Published: September 17, 2024

A rare case of late-onset immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome confused with IgA vasculitis nephropathy.

A rare case of late-onset immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome confused with IgA vasculitis nephropathy.

Journal: Pediatric nephrology (Berlin, Germany)

Published: June 11, 2024

Mitochondrial dysfunction in the pathophysiology of renal diseases.

Mitochondrial dysfunction in the pathophysiology of renal diseases.

Journal: American journal of physiology. Renal physiology

Published: March 07, 2024

Monogenic Causes Identified in 23.68% of Children with Steroid-Resistant Nephrotic Syndrome: A Single-Centre Study.

Monogenic Causes Identified in 23.68% of Children with Steroid-Resistant Nephrotic Syndrome: A Single-Centre Study.

Journal: Kidney diseases (Basel, Switzerland)

Published: July 08, 2023

A Potential Therapy Using Antisense Oligonucleotides to Treat Autosomal Recessive Polycystic Kidney Disease.

A Potential Therapy Using Antisense Oligonucleotides to Treat Autosomal Recessive Polycystic Kidney Disease.

Journal: Journal of clinical medicine

Published: December 27, 2022

Hemoperfusion and intravenous immunoglobulins for refractory gastrointestinal involvement in pediatric Henoch-Schönlein purpura: a single-center retrospective cohort study.

Hemoperfusion and intravenous immunoglobulins for refractory gastrointestinal involvement in pediatric Henoch-Schönlein purpura: a single-center retrospective cohort study.

Journal: BMC pediatrics

Published: September 07, 2022

The identification of a novel CCNQ gene tail extension variant contributing to syndactyly, telecanthus and anogenital and renal malformations syndrome.

The identification of a novel CCNQ gene tail extension variant contributing to syndactyly, telecanthus and anogenital and renal malformations syndrome.

Journal: Clinical genetics

Published: April 25, 2022

Showing 1-12 of 22

Last Updated: 09/26/2026