Mitochondrial DNA analysis in a cohort of stillbirths with brainstem and cardiac conduction system abnormalities.

Impact of compound heterozygous SDHA variants on mitochondrial function in pediatric with neurological disease.

Quantitative imaging of mitochondrial redox conditions at the single-organelle level.

Overexpression of miR-455-3p enhances mitophagy, synaptic and mitochondrial proteins in Alzheimer's disease.

Late-onset TK2 deficiency in adults: Long-term clinical outcomes of deoxynucleoside therapy.

Integrated molecular and clinical profiling of primary mitochondrial oxidative phosphorylation disorders in an Indian cohort: Insights from genetics, neuroimaging, and machine learning.

Mitochondrial DNA analysis in a cohort of stillbirths with brainstem and cardiac conduction system abnormalities.

Impact of compound heterozygous SDHA variants on mitochondrial function in pediatric with neurological disease.

Quantitative imaging of mitochondrial redox conditions at the single-organelle level.

Overexpression of miR-455-3p enhances mitophagy, synaptic and mitochondrial proteins in Alzheimer's disease.

Late-onset TK2 deficiency in adults: Long-term clinical outcomes of deoxynucleoside therapy.

Integrated molecular and clinical profiling of primary mitochondrial oxidative phosphorylation disorders in an Indian cohort: Insights from genetics, neuroimaging, and machine learning.