Tongyue Li
Beijing, China
Last Updated: 09/26/2026
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Found 10 publications
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease.
Journal: Annals of clinical and translational neurology
Published: February 14, 2026
Clinical Spectrum, Heteroplasmy-Phenotype Correlation, and Prognosis of the MT-ND3 m.10191 T > C Mutation.
Journal: CNS neuroscience & therapeutics
Published: February 10, 2026
Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease.
Journal: Orphanet journal of rare diseases
Published: July 25, 2025
Clinical, metabolic, and genetic characteristics of 42 children with mitochondrial short-chain enoyl-CoA hydratase 1 deficiency in China.
Journal: Molecular genetics and metabolism
Published: March 19, 2025
Preliminary investigation on the economic cost of mitochondrial disease in Chinese children.
Journal: Orphanet journal of rare diseases
Published: December 30, 2024
Clinical characteristics and long-term prognosis of 150 children with MELAS syndrome in China.
Journal: Journal of neurology
Published: December 18, 2024
Gender and region disparities in plasma PCSK9 levels: a systematic review and meta-analysis.
Journal: BMJ public health
Published: November 20, 2024
Posterior condylar canal dural arteriovenous fistulas.
Journal: Brain circulation
Published: May 21, 2024
Phenotypic spectrum of iron-sulfur cluster assembly gene IBA57 mutations: c.286 T > C identified as a hotspot mutation in Chinese patients with a stable natural history.
Journal: Journal of human genetics
Published: March 10, 2024
A case report of dural arteriovenous fistula with concomitant petroclival meningioma: clinical implications.
Journal: Acta neurologica Belgica
Published: January 13, 2023
Showing 1-10 of 10
Last Updated: 09/26/2026