Quantitative myotonia assessment with a commercially available dynamometer in myotonic dystrophy types 1 and 2
Author:
Affiliation:
1. Department of Neurology; University Hospital Brno; Jihlavská 20, Brno, 625 00 Czech Republic
2. Faculty of Medicine; Masaryk University; Brno Czech Republic
Funder
Ministerstvo Školství, Mládeže a Tělovýchovy
Ministerstvo Zdravotnictví Ceské Republiky
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.26401/fullpdf
Reference12 articles.
1. Prospective measurement of quality of life in myotonic dystrophy type 1;Peric;Acta Neurol Scand,2017
2. Drug treatment for myotonia;Trip;Cochrane Database Syst Rev,2006
3. Computerized hand grip myometry reliably measures myotonia and muscle strength in myotonic dystrophy (DM1);Moxley;Muscle Nerve,2007
4. Mexiletine is an effective antimyotonia treatment in myotonic dystrophy type 1 (LOE Classification);Logigian;Neurology,2010
5. A quantitative measure of handgrip myotonia in nondystrophic myotonia;Statland;Muscle Nerve,2012
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1. Tissue Doppler ultrasound of arm muscles to assess myotonia in myotonic dystrophies: An exploratory study;Muscle & Nerve;2024-08-13
2. Simple and economical HandClench Relaxometer device for reliable and sensitive measurement of grip myotonia in myotonic dystrophy;Neuromuscular Disorders;2022-04
3. Muscle Ultrasound Shear Wave Elastography as a Non-Invasive Biomarker in Myotonia;Diagnostics;2021-01-23
4. The Association of methylprednisolone dosing to cessation of myotonia in a patient with myotonic dystrophy type 1;Neuromuscular Disorders;2020-05
5. Validation of Motor Outcome Measures in Myotonic Dystrophy Type 2;Frontiers in Neurology;2020-04-21
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