Xiaoyang Lei
Guiyang, China
Last Updated: 09/26/2026
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Found 26 publications
A novel SGCE splicing variant in a Chinese family with Myoclonus-Dystonia: Rare phenotype and phenotypic variability.
Journal: Parkinsonism & related disorders
Published: May 01, 2026
Reply to: Beyond AUC: Advancing clinical interpretability of depression-MRI-machine learning analyses in Alzheimer's disease.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: March 11, 2026
Compound heterozygous PINK1 variants including a novel frameshift in a Chinese family with Parkinson's disease.
Journal: Parkinsonism & related disorders
Published: February 18, 2026
Comprehensive Characterization of Clinical Phenotypes and CTG Repeat-Associated Manifestations in Spinocerebellar Ataxia Type 8.
Journal: Cerebellum (London, England)
Published: February 02, 2026
Ribbon-Like Cortical Calcifications in Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type.
Journal: Neurology
Published: December 04, 2025
Waking up to the truth: Associations between sleep disorders and multidomain functional outcomes in Alzheimer's disease.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: November 24, 2025
Waking up to the truth: Associations between sleep disorders and multidomain functional outcomes in Alzheimer's disease.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: November 24, 2025
Renal function and cognitive performance in older adults: a NHANES-based mediation analysis of methylmalonic acid as a marker of mitochondrial dysfunction.
Journal: Renal failure
Published: November 17, 2025
Association between brain volume and depression in Alzheimer's disease: Neuroimaging insights.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: November 11, 2025
Primary central nervous system T-cell lymphoma: a single-centre retrospective study and literature review.
Journal: BMJ neurology open
Published: November 02, 2025
Ataxia with oculomotor apraxia type 2: two pedigree studies and a comprehensive review.
Journal: Journal of neurology
Published: June 11, 2025
Last Updated: 09/26/2026