Efficacy and safety of respiratory strength and endurance training in patients with myotonic dystrophy type 1 (DM1): a randomized controlled trial

Regular IMT is a feasible, safe, and effective intervention for improving respiratory function in patients with DM1. Regular RMT can enhance respiratory muscle strength and endurance and should be incorporated into the multidisciplinary care of DM1 patients showing initial signs of restrictive ventilatory insufficiency.

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Publication Details

Journal
Journal of Neurology
Published
2025-09-01
DOI
https://doi.org/10.1007/s00415-025-13362-z
Citations
2
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
1.82
Controls
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article

Efficacy and safety of respiratory strength and endurance training in patients with myotonic dystrophy type 1 (DM1): a randomized controlled trial

Stephan Wenninger, Kristina Gutschmidt, Benedikt G. H. Schoser, Natalia García-Angarita et al.
2 citations
Journal of Neurology
Genetic Neurodegenerative Diseases
1.82
article

Efficacy and safety of respiratory strength and endurance training in patients with myotonic dystrophy type 1 (DM1): a randomized controlled trial

Stephan Wenninger, Kristina Gutschmidt, Benedikt G. H. Schoser, Natalia García-Angarita, Marko Mijic, Corinna Wirner-Piotrowski, Eva Heidsieck, Daniel H Mendelshohn
article en
2 citations

Abstract

Regular IMT is a feasible, safe, and effective intervention for improving respiratory function in patients with DM1. Regular RMT can enhance respiratory muscle strength and endurance and should be incorporated into the multidisciplinary care of DM1 patients showing initial signs of restrictive ventilatory insufficiency.

Journal of NeurologyVol. 272(9)
Ludwig-Maximilians-Universität München (DE)
Openalex Percentile: Top 13%
Genetic Neurodegenerative Diseases
1.82
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