Xiaoqin Yuan

Mianyang, China

Last Updated: 09/26/2026

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Found 27 publications

Adult-onset neuronal intranuclear inclusion disease initially presenting with prominent gastrointestinal symptoms: a case report.

Adult-onset neuronal intranuclear inclusion disease initially presenting with prominent gastrointestinal symptoms: a case report.

Journal: BMC neurology

Published: November 07, 2025

Expanding the clinical phenotype of DYNC1H1 -associated mutations: a Chinese family with autosomal dominant complex hereditary spastic paraplegia.

Expanding the clinical phenotype of DYNC1H1 -associated mutations: a Chinese family with autosomal dominant complex hereditary spastic paraplegia.

Journal: BMC medical genomics

Published: September 22, 2025

Asymmetric hand deformities with limited mobility.

Asymmetric hand deformities with limited mobility.

Journal: Annals of the rheumatic diseases

Published: July 19, 2025

A novel mutation in SORD gene associated with distal hereditary motor neuropathies.

A novel mutation in SORD gene associated with distal hereditary motor neuropathies.

Journal: BMC medical genomics

Published: September 26, 2023

White Matter Characteristics of Cognitive Impairment in Tap-Test Positive Idiopathic Normal Pressure Hydrocephalus: A Diffusion Tensor Tract-Based Spatial Study.

White Matter Characteristics of Cognitive Impairment in Tap-Test Positive Idiopathic Normal Pressure Hydrocephalus: A Diffusion Tensor Tract-Based Spatial Study.

Journal: Frontiers in neuroscience

Published: September 12, 2021

Different resting-state network disruptions in newly diagnosed drug-naïve Parkinson's disease patients with mild cognitive impairment.

Different resting-state network disruptions in newly diagnosed drug-naïve Parkinson's disease patients with mild cognitive impairment.

Journal: BMC neurology

Published: April 16, 2021

Clinical Reasoning: A 24-year-old man with head tremor and decreased ceruloplasmin level.

Clinical Reasoning: A 24-year-old man with head tremor and decreased ceruloplasmin level.

Journal: Neurology

Published: August 06, 2020

Contribution of Five Functional Loci of Dopamine Metabolism-Related Genes to Parkinson's Disease and Multiple System Atrophy in a Chinese Population.

Contribution of Five Functional Loci of Dopamine Metabolism-Related Genes to Parkinson's Disease and Multiple System Atrophy in a Chinese Population.

Journal: Frontiers in neuroscience

Published: June 12, 2020

Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11.

Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11.

Journal: BMC neurology

Published: October 10, 2019

Gibberellins modulate shade-induced soybean hypocotyl elongation downstream of the mutual promotion of auxin and brassinosteroids.

Gibberellins modulate shade-induced soybean hypocotyl elongation downstream of the mutual promotion of auxin and brassinosteroids.

Journal: Plant physiology and biochemistry : PPB

Published: September 28, 2019

Primary disruption of the default mode network subsystems in drug-naïve Parkinson's disease with mild cognitive impairments.

Primary disruption of the default mode network subsystems in drug-naïve Parkinson's disease with mild cognitive impairments.

Journal: Neuroradiology

Published: September 09, 2019

Clinical disease stage related changes of serological factors in amyotrophic lateral sclerosis.

Clinical disease stage related changes of serological factors in amyotrophic lateral sclerosis.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: February 21, 2019

Showing 1-12 of 27

Last Updated: 09/26/2026