Congli Chen
Beijing, China
Last Updated: 09/26/2026
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Found 9 publications
Coexistence of T1DM and GCK-MODY: Case Report and Literature Review.
Journal: Journal of clinical research in pediatric endocrinology
Published: October 28, 2025
Pediatric floating-harbor syndrome: clinical features and treatment outcomes in a cohort of Chinese children.
Journal: European journal of pediatrics
Published: July 22, 2025
GCK Mutation Analysis and Clinical Profiles of Chinese Pediatric Patients with MODY2: Insights into Screening and Diagnosis.
Journal: Pediatric health, medicine and therapeutics
Published: May 15, 2025
Genetic Pathogenesis and Treatment of Forkhead Box A2 Hyperinsulinemia.
Journal: Endocrine, metabolic & immune disorders drug targets
Published: February 26, 2025
Clinical, genetic characteristics and outcome of four Chinese patients with Bartter syndrome type 3: Further insight into a genotype-phenotype correlation.
Journal: Molecular genetics and metabolism reports
Published: April 02, 2024
A synonymous KCNJ11 variant leading to MODY13: A case report and literature review.
Journal: Molecular genetics and metabolism reports
Published: October 22, 2023
Congenital hyperinsulinism patient with ABCC8 and KCNJ11 double heterozygous variants: a case report with 6 years follow-up.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: October 06, 2023
C.487C>T mutation in PAX4 gene causes MODY9: A case report and literature review.
Journal: Medicine
Published: January 03, 2023
Phosphomannomutase 2 hyperinsulinemia: Recent advances of genetic pathogenesis, diagnosis, and management.
Journal: Frontiers in endocrinology
Published: November 18, 2022
Showing 1-9 of 9
Last Updated: 09/26/2026