Yafei Wen

Changsha, China

Last Updated: 09/26/2026

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Found 9 publications

Reduced synaptic density in patients with progressive supranuclear palsy: An 18F-SynVest-1 PET study.

Reduced synaptic density in patients with progressive supranuclear palsy: An 18F-SynVest-1 PET study.

Journal: Parkinsonism & related disorders

Published: December 28, 2025

Differentiating progressive supranuclear palsy from other movement disorders using transcranial sonography: a systematic review and meta-analysis.

Differentiating progressive supranuclear palsy from other movement disorders using transcranial sonography: a systematic review and meta-analysis.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: July 26, 2023

Clinical features of progressive supranuclear palsy.

Clinical features of progressive supranuclear palsy.

Journal: Frontiers in aging neuroscience

Published: May 26, 2023

Ultrasonography-based radiomics and computer-aided diagnosis in thyroid nodule management: performance comparison and clinical strategy optimization.

Ultrasonography-based radiomics and computer-aided diagnosis in thyroid nodule management: performance comparison and clinical strategy optimization.

Journal: Frontiers in endocrinology

Published: January 09, 2023

Genetics of progressive supranuclear palsy in a Chinese population.

Genetics of progressive supranuclear palsy in a Chinese population.

Journal: Neurobiology of disease

Published: January 29, 2022

The Application of Deep Brain Stimulation for Progressive Supranuclear Palsy: A Systematic Review.

The Application of Deep Brain Stimulation for Progressive Supranuclear Palsy: A Systematic Review.

Journal: Frontiers in neurology

Published: December 02, 2021

Genetic effect of MTHFR C677T, A1298C, and A1793G polymorphisms on the age at onset, plasma homocysteine, and white matter lesions in Alzheimer's disease in the Chinese population.

Genetic effect of MTHFR C677T, A1298C, and A1793G polymorphisms on the age at onset, plasma homocysteine, and white matter lesions in Alzheimer's disease in the Chinese population.

Journal: Aging

Published: January 13, 2021

First case report of cerebral folate deficiency caused by a novel mutation of FOLR1 gene in a Chinese patient.

First case report of cerebral folate deficiency caused by a novel mutation of FOLR1 gene in a Chinese patient.

Journal: BMC medical genetics

Published: July 30, 2020

Lack of association between LGMN and Alzheimer's disease in the Southern Han Chinese population.

Lack of association between LGMN and Alzheimer's disease in the Southern Han Chinese population.

Journal: The European journal of neuroscience

Published: April 09, 2020

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Last Updated: 09/26/2026