Minyan Jiang

Guangzhou, 510623, China

Last Updated: 09/26/2026

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Found 19 publications

Five-year disease-modifying therapeutic experience of 102 Chinese paediatric 5q-spinal muscular atrophy: a retrospective analysis.

Five-year disease-modifying therapeutic experience of 102 Chinese paediatric 5q-spinal muscular atrophy: a retrospective analysis.

Journal: Brain communications

Published: March 27, 2025

Biochemical and molecular analysis of pediatric patients with metachromatic leukodystrophy in South China: functional characterization of five novel ARSA variants.

Biochemical and molecular analysis of pediatric patients with metachromatic leukodystrophy in South China: functional characterization of five novel ARSA variants.

Journal: Metabolic brain disease

Published: September 01, 2023

Modified nusinersen intrathecal injection method: inclusion of a septal needle-free closed infusion connector.

Modified nusinersen intrathecal injection method: inclusion of a septal needle-free closed infusion connector.

Journal: Frontiers in neurology

Published: June 04, 2023

Allogeneic hematopoietic stem cell transplantation for mucopolysaccharidosis patients: a single-center experience and assessment of quality of life.

Allogeneic hematopoietic stem cell transplantation for mucopolysaccharidosis patients: a single-center experience and assessment of quality of life.

Journal: Italian journal of pediatrics

Published: January 19, 2023

Features of liver injury in 138 Chinese patients with NICCD.

Features of liver injury in 138 Chinese patients with NICCD.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: January 17, 2023

Glucose-6-Phosphate dehydrogenase deficiency associated hemolysis in a cohort of new onset type 1 diabetes children in Guangdong province, China.

Glucose-6-Phosphate dehydrogenase deficiency associated hemolysis in a cohort of new onset type 1 diabetes children in Guangdong province, China.

Journal: Diabetology & metabolic syndrome

Published: August 09, 2021

A very rare case report of glycogen storage disease type IXc with novel PHKG2 variants.

A very rare case report of glycogen storage disease type IXc with novel PHKG2 variants.

Journal: BMC pediatrics

Published: June 17, 2021

Corrigendum for Li D, Lin Y, Huang Y, et al (2018) https://doi.org/10.1002/pd.5329.

Corrigendum for Li D, Lin Y, Huang Y, et al (2018) https://doi.org/10.1002/pd.5329.

Journal: Prenatal diagnosis

Published: January 12, 2019

Genetic analysis of 63 Chinese patients with mucopolysaccharidosis type II: Functional characterization of seven novel IDS variants.

Genetic analysis of 63 Chinese patients with mucopolysaccharidosis type II: Functional characterization of seven novel IDS variants.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: December 12, 2018

Clinical features, molecular characteristics, and treatments of a Chinese girl with sitosterolemia: A case report and literature review.

Clinical features, molecular characteristics, and treatments of a Chinese girl with sitosterolemia: A case report and literature review.

Journal: Journal of clinical lipidology

Published: July 19, 2018

Early prenatal diagnosis of lysosomal storage disorders by enzymatic and molecular analysis.

Early prenatal diagnosis of lysosomal storage disorders by enzymatic and molecular analysis.

Journal: Prenatal diagnosis

Published: September 14, 2017

Genetic and clinical characteristics of Chinese children with Glucokinase-maturity-onset diabetes of the young (GCK-MODY).

Genetic and clinical characteristics of Chinese children with Glucokinase-maturity-onset diabetes of the young (GCK-MODY).

Journal: BMC pediatrics

Published: April 09, 2017

Showing 1-12 of 19

Last Updated: 09/26/2026