Objective To examine the cognitive profile of patients with myotonic dystrophy type 1 (DM1)
on the basis of a systematic review and meta-analysis of the literature. Methods Embase …

Objective: To systematically review brain imaging studies in myotonic dystrophy type 1
(DM1). Methods: We searched Embase (index period 1974–2016) and MEDLINE (index …

Neuroimaging in myotonic dystrophies provided a major contribution to the insight into brain
involvement which is highly prevalent in these multisystemic disorders. Particular in …

Objectives Central nervous system involvement is one important clinical aspect of myotonic
dystrophy type 1 and 2 (DM1 and DM2). We assessed CNS involvement DM1 and DM2 by …

Brain involvement in myotonic dystrophy type 1 (DM1) is characterized by heterogeneous
cognitive, behavioral, and affective symptoms and imaging alterations indicative of …

Myotonic dystrophy type-1 (DM1) is a genetic multi-systemic disorder involving several
organs including the brain. Despite the heterogeneity of this condition, some patients with …

Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy that affects
multiple systems including the muscle and heart. The mutant CTG expansion at the 3′-UTR …

Antecedentes y objetivos La enfermedad de Steinert o distrofia miotónica tipo 1
(DM1),(OMIM 160900) es la miopatía más prevalente en el adulto. Es una enfermedad …

Background and objectives Steinert's disease or myotonic dystrophy type 1 (MD1),(OMIM
160900), is the most prevalent myopathy in adults. It is a multisystemic disorder with …

Abstract Myotonic Dystrophy Type 1 (DM1) is a multisystemic disease that affects gray and
white matter (WM) tissues. WM changes in DM1 include increased hyperintensities and …