Jinlong Chen

72 Guangzhou Road
Nanjing, 210008, China

Last Updated: 09/26/2026

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Found 10 publications

Clinical and genetic analysis of pediatric catecholaminergic polymorphic ventricular tachycardia: focus on sinus bradycardia and neurodevelopmental disorders.

Clinical and genetic analysis of pediatric catecholaminergic polymorphic ventricular tachycardia: focus on sinus bradycardia and neurodevelopmental disorders.

Journal: Frontiers in pediatrics

Published: January 04, 2026

Burden of Non‑Communicable Diseases Among Children and Adolescents in the Asia‑Pacific Region, 1990-2021: Analysis for the Global Burden of Diseases Study 2021.

Burden of Non‑Communicable Diseases Among Children and Adolescents in the Asia‑Pacific Region, 1990-2021: Analysis for the Global Burden of Diseases Study 2021.

Journal: Annals of global health

Published: July 28, 2025

Routine Laboratory Markers-Based Machine Learning Model for Predicting Severe Kawasaki Disease in Pediatric Patients.

Routine Laboratory Markers-Based Machine Learning Model for Predicting Severe Kawasaki Disease in Pediatric Patients.

Journal: Journal of inflammation research

Published: April 11, 2025

Relapse of Graves' disease in Chinese children: a retrospective cohort study.

Relapse of Graves' disease in Chinese children: a retrospective cohort study.

Journal: European thyroid journal

Published: March 18, 2023

Case report: Rare restrictive cardiomyopathy with ventricular fibrillation as initial symptom rescued by automatic external defibrillator in a pediatric patient.

Case report: Rare restrictive cardiomyopathy with ventricular fibrillation as initial symptom rescued by automatic external defibrillator in a pediatric patient.

Journal: Frontiers in cardiovascular medicine

Published: September 30, 2022

Case Report: Rare Iliac Vein Compression (May-Thurner) Syndrome in a Pediatric Patient.

Case Report: Rare Iliac Vein Compression (May-Thurner) Syndrome in a Pediatric Patient.

Journal: Frontiers in pediatrics

Published: April 13, 2021

Case Report: A Novel Variant c.2262+3A>T of the SCN5A Gene Results in Intron Retention Associated With Incessant Ventricular Tachycardias.

Case Report: A Novel Variant c.2262+3A>T of the SCN5A Gene Results in Intron Retention Associated With Incessant Ventricular Tachycardias.

Journal: Frontiers in medicine

Published: January 27, 2021

Case Report: Identification of Mutations in LAMP2 in Two Chinese Infants With Danon Disease.

Case Report: Identification of Mutations in LAMP2 in Two Chinese Infants With Danon Disease.

Journal: Frontiers in genetics

Published: July 31, 2020

Left Bundle Pacing for Left Bundle Branch Block and Intermittent Third-Degree Atrioventricular Block in a MYH7 Mutation-Related Hypertrophic Cardiomyopathy With Restrictive Phenotype in a Child.

Left Bundle Pacing for Left Bundle Branch Block and Intermittent Third-Degree Atrioventricular Block in a MYH7 Mutation-Related Hypertrophic Cardiomyopathy With Restrictive Phenotype in a Child.

Journal: Frontiers in pediatrics

Published: February 04, 2020

Whole-Exome Sequencing Reveals Novel Genetic Variation for Dilated Cardiomyopathy in Pediatric Chinese Patients.

Whole-Exome Sequencing Reveals Novel Genetic Variation for Dilated Cardiomyopathy in Pediatric Chinese Patients.

Journal: Pediatric cardiology

Published: August 24, 2018

Showing 1-10 of 10

Last Updated: 09/26/2026