Min-ting H. Lin
Fuzhou, China
Last Updated: 09/26/2026
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Found 54 publications
A Novel Homozygous RRP12 Variant in a Chinese Patient with Early-Onset Cerebellar Ataxia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 02, 2026
Peripheral metabolic profiles in spinocerebellar ataxia type 3: Features and genotype-phenotype links.
Journal: Parkinsonism & related disorders
Published: December 08, 2025
De Novo Facioscapulohumeral Muscular Dystrophy: A Severe Subtype Driven by D4Z4 Repeat Contractions.
De Novo Facioscapulohumeral Muscular Dystrophy: A Severe Subtype Driven by D4Z4 Repeat Contractions.
Journal: Neurology. Genetics
Published: November 10, 2025
Peripheral inflammation in spinocerebellar ataxia type 3: associations with genetic and clinical manifestations.
Journal: Inflammation research : official journal of the European Histamine Research Society ... [et al.]
Published: June 20, 2025
Parkinson's Paradox: Alpha-synuclein's Selective Strike on SNc Dopamine Neurons over VTA.
Journal: bioRxiv : the preprint server for biology
Published: April 16, 2025
Comprehensive Profiling of Annexins in Neuromuscular Disorders Reveals a Unique Signature in Dysferlinopathy.
Journal: European journal of neurology
Published: April 10, 2025
Clinical and Genetic Findings in a Chinese Cohort of Dentatorubral-Pallidoluysian Atrophy Patients.
Journal: Annals of neurology
Published: January 07, 2025
Fatigue in the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type 3.
Journal: European journal of neurology
Published: October 05, 2024
Associations between CAG repeat size, brain and spinal cord volume loss, and motor symptoms in spinocerebellar ataxia type 3: a cohort study.
Journal: Orphanet journal of rare diseases
Published: June 19, 2024
Static Posture Instability as a Sensitive Biomarker for Motor Abnormalities in Pre-ataxic Spinocerebellar Ataxia Type 3 Patients.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: May 07, 2024
Comprehensive Proteomic Analysis of Dysferlinopathy Unveiling Molecular Mechanisms and Biomarkers Linked to Pathological Progression.
Journal: CNS neuroscience & therapeutics
Published: April 11, 2024
Detection of pTDP-43 via routine muscle biopsy: A promising diagnostic biomarker for amyotrophic lateral sclerosis.
Journal: Brain pathology (Zurich, Switzerland)
Published: November 10, 2023
Last Updated: 09/26/2026