Latest News About Lafora Disease and Lafora Disease Gene Therapy Project
Here you’ll find all the latest news about the Lafora Disease and about the Gene Therapy Project. You can learn more about the disease in the Lafora Disease page.
- Rugby Perugia Supports the Baschirotto Association
Rugby Perugia is honored to support the “Mauro Baschirotto” Association for Rare Disease on the occasion of the Serie A Perugia-Prato match on Sunday 10 April 2022 - Rare Disease Day 2022: a New Research Project for Lafora Disease
Monday, 28th February 2022: today is the 15th edition of the INTERNATIONAL RARE DISEASE DAY. The Giornale di Vicenza talks about the “Mauro Baschirotto” Institute for Rare Diseases (B.I.R.D.). Rare Continue Reading - Expert Meeting – Lafora Disease and Innovative Therapies
All the informations about the “Expert Meeting: Progressive Myoclonic Epilepsies – Lafora Disease and Innovative Therapies” that will take place in Perugia and Assisi on October 4th and October 5th, 2021 - Lafora Gene Therapy Project for Federico and others
The Mauro Baschirotto Association for Rare Diseases carries out its activities both nationally and internationally. Hence the need to rethink its organizational structure, taking into account the growing needs associated Continue Reading