Kang-yang Jih
Taipei, TNQ, Taiwan
Last Updated: 09/26/2026
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Found 31 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.
Journal: Journal of the Chinese Medical Association : JCMA
Published: May 12, 2026
FUS-associated ALS in Taiwan: genetic spectrum, clinical features, and a founder haplotype of p.H517D.
Journal: Journal of neurology
Published: March 15, 2026
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
The genetic landscape of spinocerebellar ataxias in Taiwan: Insights from 876 genetically confirmed cases.
Journal: Parkinsonism & related disorders
Published: June 25, 2025
NOTCH2NLC Repeat Expansions in Parkinsonian Disorders: Clinical and Neuroimaging Characteristics.
Journal: Annals of clinical and translational neurology
Published: April 02, 2025
TARDBP variants in Taiwanese ALS patients: Genetic spectrum, clinical features, and founder effects.
TARDBP variants in Taiwanese ALS patients: Genetic spectrum, clinical features, and founder effects.
Journal: Journal of the neurological sciences
Published: March 01, 2025
The role of adiponectin-AMPK axis in TDP-43 mislocalization and disease severity in ALS.
Journal: Neurobiology of disease
Published: September 09, 2024
Investigating ITM2B-associated ataxia in a Taiwanese cerebellar ataxia cohort.
Journal: Annals of clinical and translational neurology
Published: August 23, 2024
Early presentation of spastic paraparesis in individuals carrying PSEN1 mutations: a clinical and genetic analysis.
Journal: Alzheimer's research & therapy
Published: August 13, 2024
TBK1 p.Y153Qfs*9 variant may be associated with young-onset, rapidly progressive amyotrophic lateral sclerosis through a haploinsufficiency mechanism.
Journal: Journal of the Chinese Medical Association : JCMA
Published: August 09, 2024
Neuronal Intranuclear Inclusion Disease Mimicking Chronic Inflammatory Demyelinating Polyradiculoneuropathy: A Case Report.
Journal: Acta neurologica Taiwanica
Published: June 05, 2024
Last Updated: 09/26/2026