BACKGROUND
DYT-THAP1 is a recognized cause of early-onset isolated dystonia. However, available data are largely derived from European cohorts, limiting understanding of genetic diversity, phenotype variability, and treatment response in underrepresented populations.
OBJECTIVES
To characterize the clinical spectrum,...
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The comprehensive understanding of triplet repeat expansion (TRE) disorders as monogenic neurodegenerative diseases presents a fundamental challenge for developing treatments capable of modifying the disease course, as neurogenetic research indicates. The past 30 years reveal that preclinical results demonstrating stro...
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This narrative review provides a concise, clinically oriented overview of DBS tailored for neurologists, residents, and trainees involved in the evaluation and longitudinal management of advanced PD.
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