Myotonic dystrophy type 1 as a major risk factor for severe COVID-19?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s13760-020-01514-z.pdf
Reference23 articles.
1. Buxton J, Shelbourne P, Davies J et al (1992) Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy. Nature 355:547–548. https://doi.org/10.1038/355547a0
2. Wenninger S, Montagnese F, Schoser B (2018) Core clinical phenotypes in Myotonic Dystrophies. Front. Neurol. 9:303. https://doi.org/10.3389/fneur.2018.00303
3. Poponick JM, Jacobs I, Supinski G, Dimarco AF (1997) Effect of upper respiratory tract infection in patients with neuromuscular disease. Am J Respir Crit Care Med 156:659–664. https://doi.org/10.1164/ajrccm.156.2.9611029
4. Reardon W, Newcombe R, Fenton I et al (1993) The natural history of congenital myotonic dystrophy: mortality and long term clinical aspects. Arch Dis Child 68:177–181. https://doi.org/10.1136/adc.68.2.177
5. Mier-Jedrzejowicz A, Brophy C, Green M (1988) Respiratory muscle weakness during upper respiratory tract infections. Am Rev Respir Dis 138:5–7. https://doi.org/10.1164/ajrccm/138.1.5
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