Han-lin Chiang
Taipei, TNQ, Taiwan
Last Updated: 09/26/2026
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Found 25 publications
Dystonia: from phenotypes to genetics and therapeutic advances.
Journal: Current opinion in neurology
Published: June 11, 2026
Parkinson's disease in transition: Genetics, biomarkers, and emerging therapeutics.
Journal: Journal of the Formosan Medical Association = Taiwan yi zhi
Published: September 29, 2025
Neuronal-specific antibody in patients with multiple system atrophy and progressive supranuclear palsy.
Journal: Journal of the Formosan Medical Association = Taiwan yi zhi
Published: September 12, 2025
The Effects of Biofeedback Therapy on Anxiety and Depression in Parkinson's Disease: A Pilot Study.
Journal: Journal of movement disorders
Published: April 14, 2025
NOTCH2NLC Repeat Expansions in Parkinsonian Disorders: Clinical and Neuroimaging Characteristics.
Journal: Annals of clinical and translational neurology
Published: April 02, 2025
Management of Gastrointestinal Symptoms in Parkinson's Disease.
Journal: Journal of central nervous system disease
Published: March 27, 2025
Prevalence of NOTCH2NLC and FMR1 Repeat Expansions in Atypical Parkinsonism Compared to Asymptomatic Elderly Individuals.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 17, 2025
A Randomized, Double-Blind, Placebo Controlled, Crossover Trial of incobotulinumtoxinA Treatment for Upper Limb Tremor.
Journal: Movement disorders clinical practice
Published: December 17, 2024
A single centre prospective study of three device-assisted therapies for Parkinson's disease.
Journal: NPJ Parkinson's disease
Published: November 30, 2022
Colonic Leucine-Rich Repeat Kinase 2 Expression Is Increased and Associated With Disease Severity in Patients With Parkinson's Disease.
Journal: Frontiers in aging neuroscience
Published: November 21, 2021
Transcranial Direct Current Stimulation on Different Targets to Modulate Cortical Activity and Dual-Task Walking in Individuals With Parkinson's Disease: A Double Blinded Randomized Controlled Trial.
Journal: Frontiers in aging neuroscience
Published: November 01, 2021
Expanding the phenotype of AFG3L2 mutations: Late-onset autosomal recessive spinocerebellar ataxia.
Journal: Journal of the neurological sciences
Published: April 18, 2021
Last Updated: 09/26/2026