A case of myotonic dystrophy type 1 with severe dilated cardiomyopathy: an unusual presenting manifestation of the most common muscular dystrophy in adults
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Springer Science and Business Media LLC
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https://link.springer.com/content/pdf/10.1007/s10072-024-07535-3.pdf
Reference6 articles.
1. Mahadevan MS, Yadava RS, Mandal M (2021) Cardiac pathology in myotonic dystrophy type 1. Int J Mol Sci 22:11874. https://doi.org/10.3390/ijms222111874
2. Russo V, Capolongo A, Bottino R et al (2023) Echocardiographic features of cardiac involvement in myotonic dystrophy 1: Prevalence and prognostic value. J Clin Med 12:1947. https://doi.org/10.3390/jcm12051947
3. Hamel JI (2022) Myotonic dystrophy. Continuum (Minneap Minn). 28(6):1715–1734. https://doi.org/10.1212/CON.0000000000001184
4. Souidi A, Nakamori M, Zmojdzian M, Jagla T, Renaud Y, Jagla K (2023) Deregulations of miR-1 and its target multiplexin promote dilated cardiomyopathy associated with myotonic dystrophy type 1. EMBO Rep 24:e56616. https://doi.org/10.15252/embr.202256616
5. Winters SJ (2021) Endocrine dysfunction in patients with myotonic dystrophy. J Clin Endocrinol Metab 106:2819–2827. https://doi.org/10.1210/clinem/dgab430
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1. Correction to: A case of myotonic dystrophy type 1 with severe dilated cardiomyopathy: an unusual presenting manifestation of the most common muscular dystrophy in adults;Neurological Sciences;2024-04-30
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