eanCast: Weekly Neurology

Official neurology podcast of the European Academy of Neurology (EAN). Expert talks on general neurology, stroke, dementia, epilepsy & many more. New episodes every Monday. For neurology residents, clinicians & researchers. A resource for continuing medical education and lifelong learning.

eanCast: Weekly Neurology

Latest episodes

Ep. 191: FND in children and adults: different or the same?

Ep. 191: FND in children and adults: different or the same?

39m 6s

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.

Ep. 190: Parkinson’s disease – more than a movement disorder

Ep. 190: Parkinson’s disease – more than a movement disorder

20m 29s

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.

Ep. 189: Red flags of treatable (spino)cerebellar ataxias

Ep. 189: Red flags of treatable (spino)cerebellar ataxias

45m 50s

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...

Ep. 188: Red flags of treatable rare myopathies

Ep. 188: Red flags of treatable rare myopathies

32m 53s

Moderator: Olimpia Musumeci (Messina, Italy)
Guests: Antonio Toscano (Messina, Italy), Marianne De Visser (Amsterdam, Netherlands)

In this episode, Olimpia Musumeci speaks with Antonio Toscano and Marianne de Visser about hereditary, particularly metabolic, and acquired myopathies, especially idiopathic inflammatory myopathies amenable to treatment. They review advances in pathophysiology, diagnostic approaches and novel therapies, highlighting clinical red flags and strategies that have a significant impact on timely diagnosis and management in daily neurological practice.