eanCast: Weekly Neurology

Moderator: Natalia Szejko (Warsaw, Poland)
Guests: Tammy Hedderly (London, UK), Alexander Münchau (Lübeck, Germany)

In this episode, Natalia Szejko speaks with Tammy Hedderly and Alexander Münchau about the similarities and differences in movement disorders across the lifespan. They discuss the clinical evolution of tics and stereotypies from childhood to adulthood, the distinct diagnostic implications of dystonia and parkinsonism in pediatric versus adult populations, and the importance of multidisciplinary care and acceptance-based strategies in neurological practice.

Moderator: Meagan Watson (Denver, USA)
Guests: Pavlina Danhofer (Brno, Czech Republic), Natalia Szejko (Warsaw, Poland)

In this episode, Meagan Watson speaks with Pavlína Danhofer and Natalia Szejko about whether functional neurological disorders (FNDs) present differently in children and adults. They discuss age-specific clinical features, comorbidities, developmental and family context, diagnostic challenges, and the role of early, tailored multidisciplinary management to improve outcomes in neurological practice.

In this episode, Yıldız Değirmenci speaks with Julie Hall and Marit Ruitenberg about non-motor symptoms in Parkinson’s disease, focusing on anxiety and cognitive impairment. They examine their clinical profiles, early detection challenges including neuropsychological markers, interactions with motor manifestations, and implications for comprehensive assessment and individualized management in neurological practice.

Moderator: João Durães (Coimbra, Portugal)
Guests: Paola Giunti (London, UK), Lidia Sarro (Milan, Italy)

In this episode, João Durães, Paola Giunti and Lidia Sarro provide a rigorous examination of the diagnostic and therapeutic landscape of treatable ataxias, focusing on rare variants. The discussion first delineates autoimmune etiologies, such as anti-GAD, paraneoplastic, and gluten-related syndromes, before transitioning to a detailed review of acquired and genetic metabolic disorders, including vitamin deficiencies, NPC, Refsum disease, Glut1 deficiency, CTX, and Wilson’s disease among others. By highlighting critical clinical and paraclinical "red flags," the contributors offer a framework for accelerating differential diagnosis. The session concludes...