Share4Rare webinar: Medical imaging in rare disease diagnosis
On the next Share4Rare webinar they will talk about the potential of clinical imaging in rare disease diagnosis and research. The guest speaker will be…
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On the next Share4Rare webinar they will talk about the potential of clinical imaging in rare disease diagnosis and research. The guest speaker will be…
Click here for slides Next webinar organised by ERN-RND will be on : ‘Basal ganglia diseases in childhood’ by Belén Perez Dueñas 12 April 2022,…
Thursday 7th April 2022 16:00-17:15 Paris Time by: Alessandra Ferlini, Rita Selvatici, Francesca Gualandi and Carl Fratter Dystrophin (DMD) gene pathogenic variations cause dystrophinopathies, a…
Next webinar organised by ERN-RND will be on : ‘The logopenic variant of primary progressive aphasia (lvPPA): language, cognitive, neuroradiological issues’ by Robert Rusina and…
‘Antisense oligonucleotide mediated exon skipping therapy development for Duchenne muscular dystrophy takes more than an oligonucleotide’ by Annemieke Aartsma-Rus 29 March 2022, 3-4pm CEST The…
Muscular Dystrophy UK will host a Muscles Matter Seminar on Congenital Muscular Dystrophy on Tuesday the 29th of March from 10am – 12pm CET. The…
Next webinar organised by ERN-RND will be on : ‘Measuring disease severity in chronic progressive myelopathy’ by Marc Engelen 15 March 2022, 3-4pm CET The…
Delivered by Prof Nens van Alfen Nens van Alfen MD PhD is an associate professor of Neurology and clinical neurophysiologist from the Radboud university medical…
Click here to view the webinar ‘Brain Development in Huntington’s Disease’ by Peggy Nopoulos 8 March 2022, 3-4pm CET The speaker is Professor of Psychiatry…
In the context of EJP RD’s ERN Workshops, a hybrid workshop on “contemporary outcome measures in neuromuscular diseases” aimed at understanding the advancement of technologies with digital outcome measures in neuromuscular…
Every year, Eurordis, the European Federation of Rare Disease Organizations, coordinates Rare Disease Day – the International Day for Rare Diseases – on the last…
Delivered by Prof. Rita Horvath and Dr May Yung Tiet From their paper: “Leigh syndrome (LS) is the most frequent paediatric clinical presentation of mitochondrial…