Afterdischarges in 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/s10072-023-07013-2.pdf
Reference32 articles.
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2. Hermans MC, Faber CG, Vanhoutte EK, Bakkers M, De Baets MH, de Die-Smulders CE, Merkies IS (2011) Peripheral neuropathy in myotonic dystrophy type 1. J Peripher Nerv Syst 16(1):24–29
3. Fournier E, Arzel M, Sternberg D, Vicart S, Laforet P, Eymard B, Willer JC, Tabti N, Fontaine B (2004) Electromyography guides toward subgroups of mutations in muscle channelopathies. Ann Neurol 56(5):650–661
4. Kim DS, Kim EJ, Jung DS, Park KH, Kim IJ, Kwak KY, Kim CM, Ko HY (2002) A Korean family with Arg1448Cys mutation of SCN4A channel causing paramyotonia congenita: electrophysiologic, histopathologic, and molecular genetic studies. J Korean Med Sci 17(6):856–860
5. Harrison TB, Benatar M (2007) Accuracy of repetitive nerve stimulation for diagnosis of the cramp-fasciculation syndrome. Muscle Nerve 35(6):776–780
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1. Further insights into afterdischarges as a diagnostic marker for myotonic dystrophy type 1;Neurological Sciences;2023-10-11
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