Ying Zou

Beijing, China

Last Updated: 09/26/2026

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Found 21 publications

Age-related changes in central corneal thickness and their association with ocular biometric parameters in children.

Age-related changes in central corneal thickness and their association with ocular biometric parameters in children.

Journal: Frontiers in medicine

Published: March 06, 2026

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease.

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.

Clinical Spectrum, Heteroplasmy-Phenotype Correlation, and Prognosis of the MT-ND3 m.10191 T > C Mutation.

Journal: CNS neuroscience & therapeutics

Published: February 10, 2026

Clinical phenotype spectrum and prognostic analysis of DNM1L-related disorders: a single-center cohort study of 18 patients.

Clinical phenotype spectrum and prognostic analysis of DNM1L-related disorders: a single-center cohort study of 18 patients.

Journal: Frontiers in neurology

Published: January 19, 2026

Injectable Thermogel-Loaded Bi2S3 Nanorods for Synergistic Photothermal Bacterial Elimination and Anti‑Inflammation to Remodel Periodontitis Microenvironment.

Injectable Thermogel-Loaded Bi2S3 Nanorods for Synergistic Photothermal Bacterial Elimination and Anti‑Inflammation to Remodel Periodontitis Microenvironment.

Journal: Small (Weinheim an der Bergstrasse, Germany)

Published: November 11, 2025

Genotype-Phenotype Correlations in Chinese Pediatric Patients With Single Large-Scale Mitochondrial DNA Deletion Disorders.

Genotype-Phenotype Correlations in Chinese Pediatric Patients With Single Large-Scale Mitochondrial DNA Deletion Disorders.

Journal: Clinical genetics

Published: August 01, 2025

Deficiency of the NAD(P)HX metabolic repair system: a treatable mitochondrial disease.

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.

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.

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.

Clinical characteristics and long-term prognosis of 150 children with MELAS syndrome in China.

Journal: Journal of neurology

Published: December 18, 2024

Novel pathogenic mtDNA variants in Chinese children with neurological mitochondrial disorders.

Novel pathogenic mtDNA variants in Chinese children with neurological mitochondrial disorders.

Journal: Annals of clinical and translational neurology

Published: July 05, 2024

CEO social capital and implied cost of capital: Based on the empirical evidence of Chinese family businesses.

CEO social capital and implied cost of capital: Based on the empirical evidence of Chinese family businesses.

Journal: PloS one

Published: February 28, 2024

Showing 1-12 of 21

Last Updated: 09/26/2026