Year: 2024

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Biomarkers in CMT2A patients

A new research project is underway, supported by our association and carried out by the team of Professor Stefania Corti of the Dino Ferrari Centre/University of Milan (Doctors Rizzo, Abati and Anastasia). The project aims to detect in the blood of patients with CMT2A (or other pathologies due to mutation

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Interview with Professor Comi, Director of the “Dino Ferrari Centre”

🎙️On the occasion of Rare Disease Day, which was celebrated on 29 February (“a day of a leap year, rare as the diseases we are talking about”), Professor Comi, Director of the “Dino Ferrari Centre” gave an interesting interview about rare diseases (likeCMT2A) which is, to us, like a ray of sunshine warming our

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Neuromuscular Diseases’ Day: GMN 2024

The Seventh Day of Neuromuscular Diseases – GMN 2024- will be held on April 13, 2024. The event will take place simultaneously in 19 Italian cities linked to the most important centers for the study of neuromuscular diseases: Ancona, Bari, Bologna, Brescia, Cagliari, Chieti, Genoa, Messina, Milan, Naples, Palermo, Parma,

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Rare Disease Day 2024

The countdown to celebrate Rare Disease Day 2024 has begun. Patient organizations around the world have already scheduled many events and many more are about to. Common goal? Raising public awareness and generating change for the 300 million people around the world living with a rare disease (such as CMT2A),

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CM2A: identification of a potential therapeutic approach

Before the end of the year, a very important news was given to you: the scientific journal “Cellular and Molecular Life Sciences” published the study carried out by Dr Rizzo together with the team directed by Prof.ssa Corti of the Dino Ferrari Centre/University of Milan. Combined RNA interference and gene

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