Yu-sen Qiu
Fuzhou, 350005, China
Last Updated: 09/26/2026
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Found 10 publications
Associations between CAG repeat size, brain and spinal cord volume loss, and motor symptoms in spinocerebellar ataxia type 3: a cohort study.
Journal: Orphanet journal of rare diseases
Published: June 19, 2024
Characteristics of tandem repeat inheritance and sympathetic nerve involvement in GAA-FGF14 ataxia.
Journal: Journal of human genetics
Published: February 23, 2024
Cognitive impairment associated with cerebellar volume loss in spinocerebellar ataxia type 3.
Journal: Journal of neurology
Published: July 13, 2023
Alu Retrotransposition Event in SPAST Gene as a Novel Cause of Hereditary Spastic Paraplegia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 31, 2023
Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 06, 2023
Altered brain white matter structural motor network in spinocerebellar ataxia type 3.
Journal: Annals of clinical and translational neurology
Published: August 09, 2022
Expanding the phenotype and genotype spectra of PLIN4-associated myopathy with rimmed ubiquitin-positive autophagic vacuolation.
Journal: Acta neuropathologica
Published: February 22, 2022
GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy.
Journal: Annals of neurology
Published: November 29, 2021
Novel Compound Missense and Intronic Splicing Mutation in ALDH18A1 Causes Autosomal Recessive Spastic Paraplegia.
Journal: Frontiers in neurology
Published: November 09, 2020
Showing 1-10 of 10
Last Updated: 09/26/2026