Rinaldi, Elena
Puleo, Elisa
Di Maro, Angela
Fusco, Raffaele
Canciello, Amalia
Giacopuzzi Grigoli, Eleonora
Frangiamore, Rita
Cheli, Marta
Vanoli, Fiammetta
Bonanno, Silvia
Mantegazza, Renato
Antozzi, Carlo
Baggi, Fulvio
Andreetta, Francesca
Maggi, Lorenzo https://orcid.org/0000-0002-0932-5173
Funding for this research was provided by:
Ministero della Salute
Article History
Received: 16 January 2026
Revised: 27 March 2026
Accepted: 31 March 2026
First Online: 18 April 2026
Declarations
:
: ML received honoraria for speaking, advisory boards and compensation for congress participations from Sanofi, Roche, Biogen, Amicus Therapeutics, Alexion Astrazeneca, Johnson & Johnson, Lupin, Argenx, and UCB, outside the submitted work. LM also received funding for a fellowship from Biogen and Alexion Astrazeneca. CM received honoraria for speaking from Alexion Astrazeneca, Argenx, and UCB, outside the submitted work. GGE received honoraria for participation in advisory boards for Amicus Therapeutics. MR received support for attending meetings or participation in data safety monitoring board/advisory board fees from Alexion, Argenx, Johnson & Johnson, and UCB Pharma. VF received funding for travel, speaking and advisory board from Alexion, UCB Pharma, Argenx. FR received funding for travel, consulting, meeting attendance and advisory board participation by Alexion, UCB, Argenx, Biogen, Sanofi Genzyme. CA received funding for meeting attendance, travel and advisory board participation from Alexion, UCB, Argenx, Johnson&Johnoson. BS received honoraria for speaking, advisory boards and compensation for congress participations from Sanofi, Roche, Biogen, Alexion Astrazeneca, outside the submitted work. RE, PE, FR, BF, AF, DMA, CA, have no relevant financial or non-financial interests to disclose. The authors are also part of the European Reference Network Euro-NMD.
: This retrospective study was submitted for approval to the Comitato Etico Territoriale (CET) Lombardia 4 (approval n. CET 87/24), and conducted in accordance with the principles laid down by the 18th World Medical Assembly (Declaration of Helsinki, 1964) and subsequent amendments. Due to the retrospective nature of the study, data were collected anonymously and analyzed as aggregated data. All patients signed informed consent for using their biological samples for research.