Meeting report: the 2023 FSHD international research congress
dc.contributor.authorid | 0000-0001-8202-5313 | |
dc.contributor.coauthor | Arjomand, Jamshid | |
dc.contributor.coauthor | Gabellini, Davide | |
dc.contributor.coauthor | Voermans, Nicol | |
dc.contributor.coauthor | Belayew, Alexandra | |
dc.contributor.coauthor | Bosnakovski, Darko | |
dc.contributor.coauthor | Eichinger, Katy | |
dc.contributor.coauthor | Monforte, Mauro | |
dc.contributor.coauthor | Oflazer, Piraye | |
dc.contributor.coauthor | Rosa, Alberto Luis | |
dc.contributor.department | N/A | |
dc.contributor.kuauthor | Oflazer, Piraye | |
dc.contributor.kuprofile | Faculty Member | |
dc.contributor.schoolcollegeinstitute | School of Medicine | |
dc.date.accessioned | 2025-01-19T10:33:23Z | |
dc.date.issued | 2023 | |
dc.description.abstract | Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common inherited muscular dystrophies. As part of the FSHD Society's commitment to promote global communication and collaboration among researchers, the Society collaborated with FSHD Europe and convened its 30th annual International Research Congress (IRC) on June 15–16, 2023, in the city of Milan, Italy. Over 240 researchers, clinicians, patients and pharmaceutical company representatives from a wide geographical background participated to hear about the latest developments and breakthroughs in the field. The meeting was structured to provide a mix of basic and clinical research in five sessions: 1. Discovery research & genetics; 2. Outcome assessments; 3. Disease mechanisms & interventional strategies; 4. Clinical studies & trial design; and 5. Pediatric FSHD. The keynote speakers were Professor Baziel van Engelen (on the importance of incorporating the patient's voice to help refine and improve basic laboratory and clinical research) and Dr. Bénédict Chazaud (on the role of the immune system in normal muscle regeneration and in Duchenne muscular dystrophy). The FSHD IRC was preceded by the Industry Collaborative for Therapeutic Development in FSHD meeting and followed by the World FSHD Alliance network of national patient groups and advocacy organizations for FSHD summit. The Congress concluded with the announcement for the 2024 International Research Congress, which will take place on June 13–14, 2024 in Denver, Colorado, USA, and followed by the FSHD Society's flagship educational conference for the FSHD community, the Patient Connect Conference, on June 15–16, 2024. © 2023 | |
dc.description.indexedby | WoS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.openaccess | All Open Access; Green Open Access | |
dc.description.publisherscope | International | |
dc.description.sponsors | Funding text 1: We would like to thank the following sponsors for supporting this congress: AFM Téléthon, Andrew Graham and Friends, Armatus Bio, Avidity Biosciences, Dyne Therapeutics, FSHD Europe, FSHD Global, FHSD Stichting, Fulcrum Therapeutics, James Chin, Sr. Scholarship Fund, Kate Therapeutics, miRecule, Muscular Dystrophy Association , National Institute of Health , Roche, Sanofi, The Chris Carrino Foundation for FSHD , University of Massachusetts Medical School Wellstone Center for FSHD Research , Ultragenyx, Vita Therapeutics. ; Funding text 2: We would like to thank the following sponsors for supporting this congress: AFM Téléthon, Andrew Graham and Friends, Armatus Bio, Avidity Biosciences, Dyne Therapeutics, FSHD Europe, FSHD Global, FHSD Stichting, Fulcrum Therapeutics, James Chin, Sr. Scholarship Fund, Kate Therapeutics, miRecule, Muscular Dystrophy Association, National Institute of Health, Roche, Sanofi, The Chris Carrino Foundation for FSHD, University of Massachusetts Medical School Wellstone Center for FSHD Research, Ultragenyx, Vita Therapeutics. | |
dc.description.volume | 35 | |
dc.identifier.doi | 10.1016/j.nmd.2023.10.018 | |
dc.identifier.eissn | 1873-2364 | |
dc.identifier.issn | 9608966 | |
dc.identifier.quartile | Q2 | |
dc.identifier.scopus | 2-s2.0-85177759655 | |
dc.identifier.uri | https://doi.org/10.1016/j.nmd.2023.10.018 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/26571 | |
dc.identifier.wos | 1168065000001 | |
dc.keywords | Child | |
dc.keywords | Europe | |
dc.keywords | Humans | |
dc.keywords | Italy | |
dc.keywords | Muscular Dystrophy, Duchenne | |
dc.keywords | Muscular Dystrophy, Facioscapulohumeral | |
dc.language | en | |
dc.publisher | Elsevier Ltd | |
dc.relation.grantno | Chris Carrino Foundation; FSHD; FSHD Europe; Kate Therapeutics; University of Massachusetts Medical School Wellstone Center for FSHD Research , Ultragenyx, Vita Therapeutics; University of Massachusetts Medical School Wellstone Center for FSHD Research, Ultragenyx, Vita Therapeutics; National Institutes of Health, NIH; Roche; Sanofi; Muscular Dystrophy Association, MDA | |
dc.source | Neuromuscular Disorders | |
dc.subject | Medicine | |
dc.title | Meeting report: the 2023 FSHD international research congress | |
dc.type | Conference proceeding |