Yanmei Sang

Fuxingmenwai Nanlishi Road 56, 100045
Beijing, China

Last Updated: 09/26/2026

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Found 30 publications

Multidisciplinary approach and clinical management of McCune-Albright syndrome.

Multidisciplinary approach and clinical management of McCune-Albright syndrome.

Journal: Frontiers in endocrinology

Published: January 13, 2026

Single-center experience description of surgical management of diffuse congenital hyperinsulinism in a pediatric non-current cohort.

Single-center experience description of surgical management of diffuse congenital hyperinsulinism in a pediatric non-current cohort.

Journal: Frontiers in endocrinology

Published: December 04, 2025

Coexistence of T1DM and GCK-MODY: Case Report and Literature Review.

Coexistence of T1DM and GCK-MODY: Case Report and Literature Review.

Journal: Journal of clinical research in pediatric endocrinology

Published: October 28, 2025

Novel variation in the CEL gene causing impaired fasting glucose in a Chinese pediatric patient: case report and literature review.

Novel variation in the CEL gene causing impaired fasting glucose in a Chinese pediatric patient: case report and literature review.

Journal: Frontiers in endocrinology

Published: September 16, 2025

GCK Mutation Analysis and Clinical Profiles of Chinese Pediatric Patients with MODY2: Insights into Screening and Diagnosis.

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.

Genetic Pathogenesis and Treatment of Forkhead Box A2 Hyperinsulinemia.

Journal: Endocrine, metabolic & immune disorders drug targets

Published: February 26, 2025

A new case of Rafiq syndrome with coexisting thyroid dyshormonogenesis type 6 in a Chinese patient: case report and literature review.

A new case of Rafiq syndrome with coexisting thyroid dyshormonogenesis type 6 in a Chinese patient: case report and literature review.

Journal: Frontiers in endocrinology

Published: February 25, 2025

Novel MKRN3 gene mutation associated with central precocious puberty in a Chinese child: a case report.

Novel MKRN3 gene mutation associated with central precocious puberty in a Chinese child: a case report.

Journal: Frontiers in endocrinology

Published: September 05, 2024

Central precocious puberty associated with duplicated pituitary: a case report and literature review.

Central precocious puberty associated with duplicated pituitary: a case report and literature review.

Journal: Frontiers in endocrinology

Published: July 17, 2024

Clinical, genetic characteristics and outcome of four Chinese patients with Bartter syndrome type 3: Further insight into a genotype-phenotype correlation.

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

Novel OBSL1 Variant in a Chinese Patient with 3M Syndrome: The c.458dupG Mutation May Be a Potential Hotspot Mutation in the Chinese Population

Novel OBSL1 Variant in a Chinese Patient with 3M Syndrome: The c.458dupG Mutation May Be a Potential Hotspot Mutation in the Chinese Population

Journal: Journal of clinical research in pediatric endocrinology

Published: February 26, 2024

Influence of disease course and comprehensive management on blood glucose level in children and adolescents with type 2 diabetes mellitus.

Influence of disease course and comprehensive management on blood glucose level in children and adolescents with type 2 diabetes mellitus.

Journal: Journal of diabetes investigation

Published: December 05, 2023

Showing 1-12 of 30

Last Updated: 09/26/2026