

MDS Podcast
International Parkinson and Movement Disorder Society
Stay up to date on novel, clinically-relevant research findings in Parkinson's disease and other movement disorders. Each episode of the International Parkinson and Movement Disorder Society podcast discusses a relevant development in the field, including highlighted journal articles and interviews with the authors.
Episodes
Mentioned books

Jul 1, 2024 • 0sec
Lixisenatide in Parkinson's: A Diabetes Drug to Slow Disease Progression?
Dr. Michele Matarazzo interviews Dr. Olivier Rascol on the results of the clinical trial recently published in the New England Journal of Medicine. Tune in to learn about the mechanisms of action and potential of lixisenatide and other GLP-1 receptor agonists in impacting the progression of Parkinson's disease.
Read the article »

Jun 24, 2024 • 0sec
Functional Tic-Like Behaviors: A Common Comorbidity in Patients with Tourette Syndrome
Dr. Müller-Vahl joins the podcast to discuss her retrospective study examining the key features in differentiating Tourette syndrome and Functional tic-like behaviors and that comorbidity is far more common than originally thought.
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Jun 17, 2024 • 0sec
Hot Topic: Limitations of phenomenology in functional movement disorders: what can we learn?
In this Hot Topic episode, Dr. Sarah Lidstone moderates a discussion with Dr. Mark Hallett and Prof. Mark Edwards on the limitations of phenomenology in movement disorders. Drawn from a recent viewpoint by Prof. Edwards and using functional movement disorder as an example, they discuss the benefits and drawbacks of a phenotype equaling disease paradigm, the voluntary vs. involuntary movement disorder, and what we can learn from functional movement disorders.

Jun 10, 2024 • 0sec
Understanding corticobasal syndrome: Clinical and neuroimaging characteristics to unlock the underlying pathology
Dr. Michele Matarazzo interviews Dr. Jacy Parmera about her recently published article on the clinical and neuroimaging characteristics of patients with corticobasal syndrome, with a focus on the potential correlation with the underlying neuropathological causes. Read the article »

Jun 3, 2024 • 0sec
Chorea Series: Exploring medical and surgical management for chorea
Profs. Elena Moro and Ruth Walker discuss the management of chorea, including when this is appropriate. They focus on Huntington’s disease and the role of deep brain stimulation and other surgical interventions, in addition to medical management.

May 28, 2024 • 0sec
CSF1R-related disorder in China
Dr. Sara Schaefer speaks with Doctors Xiaojun Huang and Jingying Wu about the phenotypic and genotypic spectrum of CSF1R-related disorder in a Chinese population, including unique clinical and radiographic characteristics.
Journal CME is available until May 21, 2025
Read the article.

May 20, 2024 • 0sec
Chorea Series: Approach to patients with acquired choreas
Dr. Ruth Walker and Dr. Molly Cincotta discuss causes of acquired chorea and approach to the work-up of a patient with an acquired chorea.

May 13, 2024 • 0sec
Hot Topic: Focused Ultrasound in Movement Disorders - Brain ablations as a therapeutic tool
In this Hot Topic episode, Dr. Michele Matarazzo interviews Dr. Raul Martinez on the recent evidence and future applications of focused ultrasound-based ablations in movement disorders, such as Parkinson's disease and essential tremors. Discover how this innovative approach is improving patient care and what it could mean for the future of medical treatment.

May 6, 2024 • 0sec
Chorea Series: Update on therapies for Huntington's disease
In the latest installment of the Chorea Special Series, Dr. Ruth Walker interviews Prof. Sarah Tabrizi about the current state of therapies for Huntington’s disease, and what is coming down the pipeline.

Apr 29, 2024 • 0sec
A new pathway to find structural variations in inherited neurological cases - the SCA4 example
Dr. Sarah Camargos interviews Dr. Zhonghbo Chen and Prof. Henry Houlden, first and senior author of a MDJ paper exploring a GGC repeat expansion in the ZFHX3 gene associated with spinocerebellar ataxia type 4. They describe a criative methodology to find a gene in a family with a Swedish ancestry.
Journal CME is available until April 04, 2025
Read the article.


