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 …

Myotonic dystrophy is an autosomal dominant muscular dystrophy not only associated with
muscle weakness, atrophy, and myotonia but also prominent multisystem involvement …

Myotonic dystrophy (DM) encompasses a spectrum of neuromuscular diseases
characterized by myotonia, muscle weakness, and wasting. Recent research has led to the …

Introduction Neuromuscular diseases may be of neuropsychological interest insofar as they
may affect representations based on embodied cognition theories. Previous studies have …

The myriad of neuropsychiatric manifestations reported in myotonic dystrophy type 1 may
have its origin in alterations of complex brain network interactions at the structural level. In …

Background Myotonic dystrophy type 1 (DM1) is an autosomal dominant genetic multisystem
disorder and the commonest adult-onset form of muscular dystrophy. DM1 results from the …

Background: Central nervous system involvement in myotonic dystrophy type 1 (DM1) is
associated with cognitive deficits, impaired social performance and excessive somnolence …

Abstract Myotonic Dystrophy Type 1 (DM1) is the most frequent hereditary, adult-onset
muscular dystrophy. Nevertheless, DM1-associated cognitive-motor impairments have not …

Background: In contrast to myotonic dystrophy type 1, the cognitive and radiologic profile of
myotonic dystrophy type 2 (DM2) is relatively poorly characterized. Objective: To conduct a …

Abnormalities of sleep are common in myotonic dystrophy type 1 (DM1), but few previous
studies have combined polysomnography with detailed clinical measures and brain …