[HTML][HTML] Cognitive impairment, neuroimaging abnormalities, and their correlations in myotonic dystrophy: a comprehensive review
Y Wu, Q Wei, J Lin, H Shang, R Ou - Frontiers in Cellular …, 2024 - frontiersin.org
Myotonic dystrophy (DM) encompasses a spectrum of neuromuscular diseases
characterized by myotonia, muscle weakness, and wasting. Recent research has led to the …
characterized by myotonia, muscle weakness, and wasting. Recent research has led to the …
Editorial commentary on “myotonic dystrophy type 1 (Steinert disease): 29 years of experience at a tertiary pediatric hospital”
T Sejersen - European Journal of Paediatric Neurology, 2024 - ejpn-journal.com
In this issue of EJPN, Cascais and colleagues share their longtime experience, spanning
over 29 years, of manifestations of congenital and childhood-onset myotonic dystrophy type …
over 29 years, of manifestations of congenital and childhood-onset myotonic dystrophy type …
Congenital Myotonic Dystrophy type 1: prenatal manifestations regarding a case
DL Otero, MT Licourt, BC Gómez… - SCT Proceedings in …, 2023 - proceedings.ageditor.ar
Introductions: myotonic dystrophy type 1 is a genetic disorder with great clinical variability in
which there is a positive association between the number or size of the cytosine, thymine …
which there is a positive association between the number or size of the cytosine, thymine …