
NeurologyLive® Friday 5 — April 3, 2026
Key Takeaways
- Real-world and ECTRIMS analyses indicate the 2024 McDonald criteria may improve earlier multiple sclerosis diagnosis, supporting closer alignment between trial-era definitions and routine clinical presentation.
- Individualized multiple sclerosis management requires integrating disease activity, risk tolerance, comorbidities, lifestyle, and patient preferences to optimize sequencing and long-term outcomes amid expanding therapeutic options.
Take 5 minutes to catch up on NeurologyLive®'s highlights from the week ending April 3, 2026.
Welcome to NeurologyLive®'s Friday 5! Every week, the staff compiles 5 highlights of NeurologyLive's widespread coverage in neurology, ranging from newsworthy study findings and FDA action to expert interviews and peer-to-peer panel discussions.
Click the read more or watch now buttons for more details and information about each highlight.
1: From Trial to Practice: How the 2024 Criteria Perform in Real-World Settings
In this episode of our latest NeurologyLive Roundtable Discussion, Adnan Subei, DO, FAAN, Lilyana Amezcua, MD, and Samantha Roman, MD, reviewed emerging real-world and ECTRIMS data demonstrating that the updated McDonald criteria improve earlier MS diagnosis. [WATCH TIME: 6 minutes]
2: Personalizing Treatment Decision-Making in Multiple Sclerosis Care: Constance V. Katsafanas, DO
In honor of National MS Awareness Month, held each March, Constance V. Katsafanas, DO, director of the Neurology Residency Program at the Marcus Neuroscience Institute, detailed the importance of tailoring treatment to patients with multiple sclerosis. [WATCH TIME: 5 minutes]
3: What Clinicians Should Know About Extended Dosing of Pegunigalsidase Alfa
In a recent Q&A, Rachele Berria, MD, PhD, Medical Affairs at Chiesi Global Rare Diseases, discussed the clinical data and implications of newly approved every-4-week dosing of pegunigalsidase alfa for Fabry disease in Europe.
4: Understanding the History Behind Down Syndrome and Dementia
In honor of National Down Syndrome Awareness Day, this new feature discussed how adults with Down syndrome face a high lifetime risk of early-onset Alzheimer disease linked to the triplication of chromosome 21, driving ongoing clinical investigations into therapies for this population.
5: Positioning Gene Therapy in SMA: Insights From 64-Week STEER Study Outcomes
In a recent Q&A, Nazem Atassi, MD, SVP and Global Development Head of Neurology & Gene Therapy at Novartis, discussed 64-week STEER data and the evolving role of one-time gene therapy in spinal muscular atrophy care.


















