College of Medicine
Subramony Lab
Led by Sub Subramony · Neurology
What we study
The lab studies inherited neuromuscular diseases like Friedreich ataxia and muscular dystrophies, focusing on phenotype-genotype links, biomarkers, and therapies. They run clinical trials and observational studies to improve patient care.
What working here is like
- Clinical
- Human participants
- Project
- 1
- Papers
- 5
Current projects
MOVE+ substudy
Using wearable devices to track movement in people with facioscapulohumeral muscular dystrophy.
Summaries are written by AI in plain language from public symposium abstracts and may be imperfect.
Recent papers, explained
- Effectiveness of Levodopa/Carbidopa in Slowing the Progression of MJD/SCA3
2026 · Neurology Open Access
Looks at whether levodopa/carbidopa slows disease progression in MJD/SCA3 by studying patients' natural history.
- Longitudinal Psychometric Properties of the Myotonic Dystrophy Health Index in a Large Multicenter Cohort of People Living With Myotonic Dystrophy Type 1
2026 · Muscle & Nerve
Checks how well a health survey works over time in myotonic dystrophy patients to measure disease impact.
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- Neurochemical Endpoints to Inform Early‐Stage Trials of Spinocerebellar Ataxia 2 and 3 in a Multisite Setting
2026 · Annals of Clinical and Translational Neurology
Tests brain chemical levels in SCA2 and SCA3 patients using MRI to check if they can be used as trial markers.
- Assessing airway clearance dysfunction in Friedreich’s ataxia: A focus on peak cough flow
2026 · Journal of Neuromuscular Diseases
Measures cough strength in Friedreich’s ataxia patients to see if it relates to lung or mouth strength, disease severity, or genetics.
- A deep learning framework for automated cervical spinal cord vertebral labeling and morphometric extraction from brain MRI with large-scale multicenter validation
2026 · npj Digital Medicine
Developed an AI system to automatically label and measure spinal cord vertebrae in brain scans.
Plain-language summaries are AI-written and reviewed by us; check the paper for details.
How to reach out
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