As part of Genetics Month, EURO-NMD is pleased to host a four-episode webinar series bringing together clinicians, researchers and experts involved in genetics and rare neuromuscular diseases.
Throughout every Thursday in February 2026, these webinars will provide an opportunity to share experiences, discuss current practices and explore how genetics is shaping diagnosis, care pathways, emerging therapies, and the impact of newborn screening on rare diseases.
Each session combines scientific insight with practical perspectives, fostering knowledge exchange across the European research and clinical community.
This webinar series is organised in partnership with ERN-RND for Rare Neurological Disorders and the European Academy of Neurology (EAN).
Programme
Episode 1:
Thursday, 5 February 2026 | 16:00 – 17:00 CET
Title: ERDERA Diagnostic Research Workstream
Speaker: Dr. Ana Topf, Newcastle University, UK
Moderator: Dr. Massimiliano Filosto, University of Brescia, Italy
Episode 2:
Thursday, 12 February 2026 | 16:00 – 17:00 CET
Title: CPMS Use and Value for Genetic Case Discussions
Speaker: Dr. Fernanda Fortunato, University Hospital St Anna, Ferrara, Italy
Moderator: Prof. Alessandra Ferlini, University Hospital St Anna, Ferrara, Italy
Episode 3:
Thursday, 19 February 2026 | 16:00 – 17:00 CET
Title: Genetics of Amyotrophic Lateral Sclerosis and Impact on New Therapies
Speaker: Dr. Marcella Neri, University Hospital St Anna, Ferrara, Italy
Moderator: Prof. Gabriele Siciliano, University of Pisa, Italy
Episode 4:
Thursday, 26 February 2026 | 16:00 – 17:00 CET
Title: Newborn Screening and Impact on Rare Diseases
Speaker: Prof. Jim Bonham, President of the International Society of Neonatal Screening
Moderator: Prof. Alessandra Ferlini, University Hospital St Anna, Ferrara, Italy