Further insights into afterdischarges as a diagnostic marker for myotonic dystrophy type 1
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-023-07121-z.pdf
Reference4 articles.
1. Yang L, Chen X, Wu R (2023) Afterdischarges in myotonic dystrophy type 1. Neurol Sci. https://doi.org/10.1007/s10072-023-07013-2
2. Hutto SK, Harrison TB (2021) Electrodiagnostic Assessment of Hyperexcitable Nerve Disorders. Neurol Clin 39(4):1083–1096. https://doi.org/10.1016/j.ncl.2021.06.009
3. Bae JS, Kim SG, Lim JC, Chung EJ, Kim OK (2011) Peripheral nerve axon involvement in myotonic dystrophy type 1, measured using the automated nerve excitability test. J Clin Neurol 7(2):90–95. https://doi.org/10.3988/jcn.2011.7.2.90
4. Krishnan AV, Kiernan MC (2006) Axonal function and activity-dependent excitability changes in myotonic dystrophy. Muscle Nerve 33(5):627–636. https://doi.org/10.1002/mus.20516
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