Yuning X. Sun
No.1665, Kongjiang Road
Shanghai, 200092, China
Shanghai, 200092, China
Last Updated: 09/26/2026
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Found 23 publications
Assessment of blood cobalt levels and safety of long-term hydroxocobalamin therapy in patients with cblC defect.
Journal: Frontiers in nutrition
Published: March 31, 2026
Energy Compensation Strategy: The Frontier of Neurodegenerative Disease Treatment.
Journal: ACS chemical neuroscience
Published: March 12, 2026
Sequential Mitochondrial Transplantation for Myocardial Ischemia-Reperfusion Injury Treatment.
Journal: ACS nano
Published: December 01, 2025
Clinical and genetic analyses of 17 Chinese patients with glycogen storage disease type IXc.
Journal: Orphanet journal of rare diseases
Published: August 05, 2025
Clinical, biochemical and genetic characteristics of patients with argininosuccinate lyase deficiency from a single center cohort in China.
Journal: Orphanet journal of rare diseases
Published: April 16, 2025
Long-Read Sequencing Solves Complex Structure of CYP21A2 in a Large 21-Hydroxylase Deficiency Cohort.
Journal: The Journal of clinical endocrinology and metabolism
Published: March 07, 2024
Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndrome.
Journal: Orphanet journal of rare diseases
Published: October 11, 2023
Clinical profile, genetic spectrum and therapy evaluation of 19 Chinese pediatric patients with lipoprotein lipase deficiency.
Journal: Journal of clinical lipidology
Published: February 09, 2023
Genetic and phenotypic spectrum of non-21-hydroxylase-deficiency primary adrenal insufficiency in childhood: data from 111 Chinese patients.
Journal: Journal of medical genetics
Published: September 19, 2022
Clinical and genetic characteristics of 42 Chinese paediatric patients with X-linked adrenal hypoplasia congenita.
Journal: Orphanet journal of rare diseases
Published: July 12, 2022
Last Updated: 09/26/2026