Xutong Zhao
Beijing, China
Last Updated: 09/26/2026
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Found 9 publications
Demographic characteristics, diagnostic challenges, treatment patterns, and caregiver burden of mitochondrial diseases: a retrospective cross-sectional study.
Journal: Orphanet journal of rare diseases
Published: February 06, 2024
The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions.
Journal: Molecular genetics & genomic medicine
Published: May 12, 2023
Patterns of myelinated nerve fibers loss in transthyretin amyloid polyneuropathy and mimics.
Journal: Annals of clinical and translational neurology
Published: February 15, 2022
Widespread Mislocalization of FUS Is Associated With Mitochondrial Abnormalities in Skeletal Muscle in Amyotrophic Lateral Sclerosis With FUS Mutations.
Journal: Journal of neuropathology and experimental neurology
Published: February 09, 2022
Circulating cell-free mtDNA release is associated with the activation of cGAS-STING pathway and inflammation in mitochondrial diseases.
Journal: Journal of neurology
Published: January 24, 2022
Skeletal Muscle Involvement Pattern of Hereditary Transthyretin Amyloidosis: A Study Based on Muscle MRI.
Journal: Frontiers in neurology
Published: January 09, 2022
Novel and recurrent nuclear gene variations in a cohort of Chinese progressive external ophthalmoplegia patients with multiple mtDNA deletions.
Journal: Molecular genetics & genomic medicine
Published: October 13, 2021
Appendicular skeletal muscle mass: A more sensitive biomarker of disease severity than BMI in adults with mitochondrial diseases.
Journal: PloS one
Published: March 24, 2019
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Last Updated: 09/26/2026