Fangfei Li
Beijing, China
Last Updated: 09/26/2026
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Found 10 publications
Machine learning models for the prediction of levodopa response to tremor in Parkinson's disease.
Journal: Frontiers in aging neuroscience
Published: August 21, 2025
Dorsal hyperintensity and iron deposition patterns in the substantia nigra of Parkinson's disease, idiopathic REM sleep behavior disorder, and Parkinson-plus syndromes at 7T MRI: a prospective diagnostic study.
Journal: Translational neurodegeneration
Published: February 24, 2025
Method of Tremor Levodopa Responsiveness Assessment and Its Correlation With Clinical Factors in Parkinson's Disease: Outcomes of the Acute Levodopa Challenge Test.
Journal: Parkinson's disease
Published: June 22, 2024
Prevalence and Clinical Characteristics of Dementia and Cognitive Impairment in Multiple System Atrophy: A Systematic Review and Meta-Analysis.
Journal: Journal of Parkinson's disease
Published: November 07, 2022
Prevalence of axial postural abnormalities and their subtypes in Parkinson's disease: a systematic review and meta-analysis.
Journal: Journal of neurology
Published: June 21, 2022
Association with CYP2C19 polymorphisms and Clopidogrel in treatment of elderly stroke patients.
Journal: BMC neurology
Published: December 20, 2020
Detection of α-synuclein oligomers in red blood cells as a potential biomarker of Parkinson's disease.
Journal: Neuroscience letters
Published: March 03, 2015
The diagnostic value of minor salivary gland biopsy in clinically diagnosed patients with Parkinson's disease: comparison with DAT PET scans.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: January 31, 2015
Risk factors and safe dosage of levodopa for wearing-off phenomenon in Chinese patients with Parkinson's disease.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: December 08, 2014
Molecular analysis of the SMN gene mutations in spinal muscular atrophy patients in China.
Journal: Genetics and molecular research : GMR
Published: October 03, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026