Yi-chung Lee

Taipei, TNQ, Taiwan

Last Updated: 09/26/2026

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Found 136 publications

Clinical and genetic characterization of hereditary spastic paraplegia type 4 in a Taiwanese cohort.

Clinical and genetic characterization of hereditary spastic paraplegia type 4 in a Taiwanese cohort.

Journal: Parkinsonism & related disorders

Published: May 25, 2026

Clinical and electrophysiological features for differentiating MMN from hand-onset ALS.

Clinical and electrophysiological features for differentiating MMN from hand-onset ALS.

Journal: Journal of the Chinese Medical Association : JCMA

Published: May 12, 2026

An in trans NOTCH3 loss-of-function variant modifies disease severity in CADASIL: A family-based study.

An in trans NOTCH3 loss-of-function variant modifies disease severity in CADASIL: A family-based study.

Journal: Journal of the Chinese Medical Association : JCMA

Published: April 08, 2026

FUS-associated ALS in Taiwan: genetic spectrum, clinical features, and a founder haplotype of p.H517D.

FUS-associated ALS in Taiwan: genetic spectrum, clinical features, and a founder haplotype of p.H517D.

Journal: Journal of neurology

Published: March 15, 2026

Association of imaging-defined brain age with disease severity and adverse outcomes in CADASIL.

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.

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

SOD1 mutations in Taiwanese ALS patients: Clinical characteristics, frequency, and a p.T138R founder effect.

SOD1 mutations in Taiwanese ALS patients: Clinical characteristics, frequency, and a p.T138R founder effect.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: December 22, 2025

Efficacy and Safety of Vutrisiran in Patients with Hereditary Transthyretin-mediated Amyloidosis with Polyneuropathy: Analysis of the East Asian Subpopulation from HELIOS-A.

Efficacy and Safety of Vutrisiran in Patients with Hereditary Transthyretin-mediated Amyloidosis with Polyneuropathy: Analysis of the East Asian Subpopulation from HELIOS-A.

Journal: Neurology and therapy

Published: December 05, 2025

Dietary restriction mitigates cognitive impairments in a mouse model of SCA19/22.

Dietary restriction mitigates cognitive impairments in a mouse model of SCA19/22.

Journal: Mechanisms of ageing and development

Published: October 17, 2025

Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia.

Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: September 24, 2025

Commissural Fiber Disruption Is Associated With Symptom Onset in Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy.

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

Small Vessel Disease Phenotype Associated With Monoallelic NOTCH3 Loss-of-Function Variants.

Small Vessel Disease Phenotype Associated With Monoallelic NOTCH3 Loss-of-Function Variants.

Journal: Neurology

Published: August 29, 2025

Showing 1-12 of 136

Last Updated: 09/26/2026