Meeting report: the 2023 FSHD international research congress

dc.contributor.authorid0000-0001-8202-5313
dc.contributor.coauthorArjomand, Jamshid
dc.contributor.coauthorGabellini, Davide
dc.contributor.coauthorVoermans, Nicol
dc.contributor.coauthorBelayew, Alexandra
dc.contributor.coauthorBosnakovski, Darko
dc.contributor.coauthorEichinger, Katy
dc.contributor.coauthorMonforte, Mauro
dc.contributor.coauthorOflazer, Piraye
dc.contributor.coauthorRosa, Alberto Luis
dc.contributor.departmentN/A
dc.contributor.kuauthorOflazer, Piraye
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.date.accessioned2025-01-19T10:33:23Z
dc.date.issued2023
dc.description.abstractFacioscapulohumeral 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.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessAll Open Access; Green Open Access
dc.description.publisherscopeInternational
dc.description.sponsorsFunding 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.volume35
dc.identifier.doi10.1016/j.nmd.2023.10.018
dc.identifier.eissn1873-2364
dc.identifier.issn9608966
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85177759655
dc.identifier.urihttps://doi.org/10.1016/j.nmd.2023.10.018
dc.identifier.urihttps://hdl.handle.net/20.500.14288/26571
dc.identifier.wos1168065000001
dc.keywordsChild
dc.keywordsEurope
dc.keywordsHumans
dc.keywordsItaly
dc.keywordsMuscular Dystrophy, Duchenne
dc.keywordsMuscular Dystrophy, Facioscapulohumeral
dc.languageen
dc.publisherElsevier Ltd
dc.relation.grantnoChris 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.sourceNeuromuscular Disorders
dc.subjectMedicine
dc.titleMeeting report: the 2023 FSHD international research congress
dc.typeConference proceeding

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