Multiorgan Involvement and Mortality in Individuals With Adult‐Onset Myotonic Dystrophy (<scp>DM1</scp>)—A Danish Register‐Based Study I
Despite adult-onset DM1 often being characterized as mild, comorbidities and an excess risk of death are major concerns. This calls for attention from health professionals to improve rehabilitation and survival for this population.
Authors
- John Vissing (ORCID: https://orcid.org/0000-0001-6144-8544)
- Pia Dreyer (ORCID: https://orcid.org/0000-0002-3581-7438)
- Charlotte Handberg (ORCID: https://orcid.org/0000-0002-1378-2449)
- Ulla Werlauff (ORCID: https://orcid.org/0000-0002-5294-2046)
- Hanne Aagaard (ORCID: https://orcid.org/0000-0002-7810-9298)
- Charlotte Dahl Rossau
- Jens Olsen (ORCID: https://orcid.org/0000-0002-6847-1736)
- Henning Andersen
- Jan Håkon Rudolfsen (ORCID: https://orcid.org/0000-0002-4058-056X)
- Sven Bengtsson
Institutions
- Aarhus University (DK)
- Aarhus University Hospital (DK)
- Copenhagen University Hospital (DK)
- Rigshospitalet (DK)
Publication Details
- Journal
- European Journal of Neurology
- Published
- 2025-04-01
- DOI
- https://doi.org/10.1111/ene.70135
- Citations
- 5
- Primary Topic
- Genetic Neurodegenerative Diseases
- Type
- article
- Field-Weighted Citation Impact
- 4.55