Comparison of Two Questionnaires for Sleep‐Related Symptoms in Pediatric and Adult Patients With Myotonic Dystrophy Type 1

The integration of the ESS and the FOSQ-10 allowed for a more comprehensive assessment of fatigue, a well-documented symptom in DM1 and one that the ESS alone might not fully capture. Our findings highlight the importance of incorporating multiple tools to assess sleep-related symptoms in DM1 patients.

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Publication Details

Journal
Muscle & Nerve
Published
2025-02-07
DOI
https://doi.org/10.1002/mus.28371
Citations
1
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.91
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article

Comparison of Two Questionnaires for Sleep‐Related Symptoms in Pediatric and Adult Patients With Myotonic Dystrophy Type 1

Grace Paul, Megan A. Waldrop, Eleonora S. D’Ambrosio, Shannon Chagat et al.
1 citations
Muscle & Nerve
Genetic Neurodegenerative Diseases
0.91
article

Comparison of Two Questionnaires for Sleep‐Related Symptoms in Pediatric and Adult Patients With Myotonic Dystrophy Type 1

Grace Paul, Megan A. Waldrop, Eleonora S. D’Ambrosio, Shannon Chagat, Megan Rose
article en
1 citations

Abstract

The integration of the ESS and the FOSQ-10 allowed for a more comprehensive assessment of fatigue, a well-documented symptom in DM1 and one that the ESS alone might not fully capture. Our findings highlight the importance of incorporating multiple tools to assess sleep-related symptoms in DM1 patients.

Muscle & NerveVol. 71(4)
Nationwide Children's Hospital (US), The Ohio State University Wexner Medical Center (US)
Good health and well-being
Openalex Percentile: Top 31%
Genetic Neurodegenerative Diseases
0.91
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