Chao-chun Zou

No. 3333 Binsheng Road
Hangzhou, 310052, China

Last Updated: 09/26/2026

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Found 16 publications

Beyond cholesterol: regression of carotid plaques in an adolescent-a case report.

Beyond cholesterol: regression of carotid plaques in an adolescent-a case report.

Journal: European heart journal. Case reports

Published: May 01, 2026

Genetic and Clinical Characteristics of Chromosome 15q11-q13 Duplication Syndrome in Chinese Children.

Genetic and Clinical Characteristics of Chromosome 15q11-q13 Duplication Syndrome in Chinese Children.

Journal: American journal of medical genetics. Part A

Published: January 16, 2026

Food responsiveness, addiction, and hyperphagia in Prader-Willi syndrome: a cross-sectional study of 210 Chinese patients.

Food responsiveness, addiction, and hyperphagia in Prader-Willi syndrome: a cross-sectional study of 210 Chinese patients.

Journal: Frontiers in endocrinology

Published: July 13, 2025

Safety and efficacy of laronidase in Chinese patients with mucopolysaccharidosis type I: a phase IV, single-arm, open-label, multicenter study.

Safety and efficacy of laronidase in Chinese patients with mucopolysaccharidosis type I: a phase IV, single-arm, open-label, multicenter study.

Journal: Orphanet journal of rare diseases

Published: October 23, 2024

Genotype and phenotype in patients with ACAN gene variants: Three cases and literature review.

Genotype and phenotype in patients with ACAN gene variants: Three cases and literature review.

Journal: Molecular genetics & genomic medicine

Published: July 10, 2023

Sepsis-induced Pancytopenia in an Adolescent Girl with Thyroid Storm: A Case Report

Sepsis-induced Pancytopenia in an Adolescent Girl with Thyroid Storm: A Case Report

Journal: Journal of clinical research in pediatric endocrinology

Published: April 19, 2023

Case Report: De novo variant in myelin regulatory factor in a Chinese child with 46,XY disorder/difference of sex development, cardiac and urogenital anomalies, and short stature.

Case Report: De novo variant in myelin regulatory factor in a Chinese child with 46,XY disorder/difference of sex development, cardiac and urogenital anomalies, and short stature.

Journal: Frontiers in pediatrics

Published: August 25, 2022

Recombinant Human Growth Hormone Therapy for Childhood Trichorhinophalangeal Syndrome Type I: A Case Report.

Recombinant Human Growth Hormone Therapy for Childhood Trichorhinophalangeal Syndrome Type I: A Case Report.

Journal: Children (Basel, Switzerland)

Published: August 06, 2022

Case Report: Mucolipidosis II and III Alpha/Beta Caused by Pathogenic Variants in the GNPTAB Gene (Mucolipidosis).

Case Report: Mucolipidosis II and III Alpha/Beta Caused by Pathogenic Variants in the GNPTAB Gene (Mucolipidosis).

Journal: Frontiers in pediatrics

Published: January 11, 2022

Application of next generation sequencing in the screening of monogenic diseases in China, 2021: a consensus among Chinese newborn screening experts.

Application of next generation sequencing in the screening of monogenic diseases in China, 2021: a consensus among Chinese newborn screening experts.

Journal: World journal of pediatrics : WJP

Published: October 04, 2021

6q25.1-q25.3 Microdeletion in a Chinese Girl

6q25.1-q25.3 Microdeletion in a Chinese Girl

Journal: Journal of clinical research in pediatric endocrinology

Published: May 09, 2020

Clinical features and genetic analysis of childhood sitosterolemia: Two case reports and literature review.

Clinical features and genetic analysis of childhood sitosterolemia: Two case reports and literature review.

Journal: Medicine

Published: April 16, 2019

Showing 1-12 of 16

Last Updated: 09/26/2026