Luca Marsili, MD
@LucaMarsili1
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Neurologist, Movement Disorders Specialist
Cincinnati, OH
Joined April 2019
RT @UCMovDis: Congratulations to Dr. @LucaMarsili1 and Drs. @MatteoBologn @LuciaRicciard10 on the publication of “Il Volto delle Neuroscien….
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RT @UCMovDis: Teaching case: Cerebellar ataxia and Hypomyelinating Leukodystrophy in POLR3B variant seen in our neurogenetics clinic. Lin….
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RT @NeuroHNetwork: 1/6 Have you thought about what Faces tell us about Neuroscience and what Neuroscience tells us about Faces?. Dr. Luca M….
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Take-home message:.Computer Vision is a powerful ally for diagnosing and tracking movement disorders — but to bring it into everyday care, we need standardization, validation, and clinical integration.
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⚖️ Strong agreement with clinical scales & sensor data.📹 Enables non-invasive, continuous, real-world monitoring.But we’re not there yet:.⚠️ Lack of video recording standards.🌍 Low dataset diversity.🧩 Non-motor symptoms often missed.🔌 Poor interoperability between platforms.
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Here’s what we found:.🔍 CV detects Parkinson’s & more with >80% accuracy.🧠 Most studied disorder: Parkinson’s Disease (75%).🦿 Main motor tasks: gait, finger tapping, facial expressions, tremor.🧰 Most used tools: OpenPose, MediaPipe, DeepLabCut.
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AI is driving a transformative role in movement disorders. In our latest systematic review published in Movement Disorders Clinical Practice, we analyzed 71 studies on Computer Vision (CV) for movement disorders. Pecoraro et al. Mov Disord Clin Practice.
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RT @UCMovDis: Our own Dr. @LucaMarsili1 will be chairing the session titled “From Genetics to Targeted Therapy” at the 30th World Congress….
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The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population | npj Parkinson's Disease
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RT @JackyGanguly: Differentials of L-dopa responsive juvenile onset Dystonia- Parkinsonism.# To keep Juvenile form of NIID in this list wit….
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RT @Marcelokauffman: Just published in Neurology: "Clinical Reasoning: Juvenile-Onset Dopa-Responsive Dystonia—Until It Isn't" - a fascinat….
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We always learn from our errors!.Clinical reasoning is fundamental to achieve the correct diagnosis, also in rare movement disorders.@AlbertoEspay @Marcelokauffman @pasq_peco .
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RT @Marcelokauffman: We are working with @LucaMarsili1 from @UCMovDis in better characterising CACNA1A mutations in #ataxias. Emerging evid….
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RT @Marcelokauffman: We have been discussing during my visit at @UCMovDis with @AlbertoEspay and @LucaMarsili1 about the often under-diag….
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RT @UCMovDis: It has led to a @UCincyMedicine neuro genetics clinic with a comprehensive protocol for the study of rare disorders. @LucaMar….
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RT @UCMovDis: One of our absolute favorite visiting professors, Prof. @Marcelokauffman on his 10th visit to @uofcincy. Diagnosis and caus….
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RT @UCMovDis: Our own Drs. @LucaMarsili1 and @AlbertoEspay join swords with Dr. @MatteoBologn in this review on treatment of motor symptoms….
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RT @AtaxiasARG: Studying Rare Movement Disorders: From WES to New Diagnostic and Therapeutic Approaches in a Modern Genetic Clinic. The mos….
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