Xiaosheng Zheng

88 Jiefang Road
Hangzhou, 310009, China

Last Updated: 09/26/2026

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Found 37 publications

ATP13A2 restrains macrophage NLRP3 inflammasome activation to repress neurodegeneration via modulating mitochondrial homeostasis.

ATP13A2 restrains macrophage NLRP3 inflammasome activation to repress neurodegeneration via modulating mitochondrial homeostasis.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: March 17, 2026

Novel Variants in DCTN1 Associated with Perry Disease: A Case Series from a Chinese Parkinsonism Cohort.

Novel Variants in DCTN1 Associated with Perry Disease: A Case Series from a Chinese Parkinsonism Cohort.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 02, 2026

Brain calcification-associated JAM2 pathogenic mutations impair JAM2-JAM3 tight junction structure and the blood-brain barrier integrity.

Brain calcification-associated JAM2 pathogenic mutations impair JAM2-JAM3 tight junction structure and the blood-brain barrier integrity.

Journal: Brain pathology (Zurich, Switzerland)
Published: November 16, 2025

Independent Validation and Structural Characterization of Expanded HSF1 Intronic Variable Number Tandem Repeats in Essential Tremor.

Independent Validation and Structural Characterization of Expanded HSF1 Intronic Variable Number Tandem Repeats in Essential Tremor.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: November 11, 2025

Biallelic SYNJ1 Variants in a patient with multiple system atrophy mimic syndrome.

Biallelic SYNJ1 Variants in a patient with multiple system atrophy mimic syndrome.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: October 29, 2025

A Complex FGF14 (TTC)/(TGC) Repeat Expansion in Parkinson's Disease.

A Complex FGF14 (TTC)/(TGC) Repeat Expansion in Parkinson's Disease.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 08, 2025

Teaching NeuroImage: X-Linked Adrenoleukodystrophy With Rare Temporal Pole Involvement.

Teaching NeuroImage: X-Linked Adrenoleukodystrophy With Rare Temporal Pole Involvement.

Journal: Neurology
Published: July 22, 2025

Genetic and Phenotypic Overlap Between Primary Brain Calcification and Paroxysmal Dyskinesia.

Genetic and Phenotypic Overlap Between Primary Brain Calcification and Paroxysmal Dyskinesia.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 03, 2025

A case report of a family with Primary familial brain calcification caused by a novel MYORG gene variants

A case report of a family with Primary familial brain calcification caused by a novel MYORG gene variants

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 24, 2025

Correlation of MRI Markers with Clinical Features in Multiple System Atrophy.

Correlation of MRI Markers with Clinical Features in Multiple System Atrophy.

Journal: AJNR. American journal of neuroradiology
Published: April 13, 2025

Expert Commentary for "A case of spinocerebellar ataxia type 8 with clinical manifestations as Parkinson's disease".

Expert Commentary for "A case of spinocerebellar ataxia type 8 with clinical manifestations as Parkinson's disease".

Journal: Parkinsonism & related disorders
Published: April 01, 2025

Novel SPR mutation in first Chinese patient with sepiapterin reductase deficiency: urinary biomarker validation in oldest treated case.

Novel SPR mutation in first Chinese patient with sepiapterin reductase deficiency: urinary biomarker validation in oldest treated case.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: February 12, 2025
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Last Updated: 09/26/2026