Shao-lun Hsu
TPQ, Taiwan
Last Updated: 09/26/2026
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Found 16 publications
Association of imaging-defined brain age with disease severity and adverse outcomes in CADASIL.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: February 03, 2026
Diagnostic Value and Clinical Significance of Temporopolar White-Matter Hyperintensities in CADASIL and Sporadic Small-Vessel Disease.
Journal: Journal of clinical neurology (Seoul, Korea)
Published: December 26, 2025
Commissural Fiber Disruption Is Associated With Symptom Onset in Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy.
Journal: Journal of the American Heart Association
Published: August 29, 2025
Disease Severity Staging System for NOTCH3-Associated Small Vessel Disease, Including CADASIL.
Journal: JAMA neurology
Published: November 29, 2024
Cerebral microbleeds in Taiwanese patients with neuronal intranuclear inclusion disease.
Journal: Brain : a journal of neurology
Published: September 22, 2024
Impaired cerebral interstitial fluid dynamics in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy.
Journal: Brain communications
Published: August 30, 2023
Biallelic DDHD2 mutations in patients with adult-onset complex hereditary spastic paraplegia.
Journal: Annals of clinical and translational neurology
Published: May 03, 2023
NOTCH2NLC GGC Repeat Expansion in Patients With Vascular Leukoencephalopathy.
Journal: Stroke
Published: March 21, 2023
Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 06, 2023
Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia.
Journal: Annals of clinical and translational neurology
Published: October 01, 2022
Investigating KIF1A mutations in a Taiwanese cohort with hereditary spastic paraplegia.
Journal: Parkinsonism & related disorders
Published: June 14, 2022
Assessing the NOTCH2NLC GGC repeat expansion in Taiwanese patients with hereditary spastic paraplegia.
Journal: Parkinsonism & related disorders
Published: December 19, 2021
Last Updated: 09/26/2026