Shih-chun Lan
TPQ, Taiwan
Last Updated: 09/26/2026
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Found 9 publications
Mitochondrial complex III deficiency nuclear type 2: a case report and analysis of clinical onset age-related phenotypic features.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: April 17, 2026
Claval Hypertrophy with Persistent Diffusion Restriction in PLA2G6-Associated Neurodegeneration.
Journal: Movement disorders clinical practice
Published: November 04, 2025
CHD8 -Related Neurodevelopmental Disorder Manifesting Adult-Onset Compulsive Behaviors.
Journal: Clinical genetics
Published: October 19, 2025
The genetic landscape of spinocerebellar ataxias in Taiwan: Insights from 876 genetically confirmed cases.
Journal: Parkinsonism & related disorders
Published: June 25, 2025
Spinocerebellar Ataxia 44 Caused by a Novel GRM1 Variant: Reviewing the Contrasting Pathogenic Mechanisms Underlying Two GRM1-Associated Hereditary Ataxias.
Journal: Cerebellum (London, England)
Published: April 02, 2025
Phenotypic and molecular characterization of a recurrent SPTAN1 mutation causing SPG91.
Journal: Molecular biology reports
Published: March 29, 2025
Acute necrotizing encephalopathy in adult patients with influenza: a case report and review of the literature.
Journal: BMC infectious diseases
Published: June 19, 2024
Spontaneous splenic rupture as the first clinical manifestation of Niemann-Pick disease type B: A case report and review of the literature.
Journal: Journal of clinical lipidology
Published: March 10, 2022
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Last Updated: 09/26/2026