Aim To investigate the psychiatric and cognitive phenotype in young individuals with the
childhood form of myotonic dystrophy type 1 (DM1). Method Twenty‐eight individuals (15 …

Increasing evidences indicate that in Myotonic Dystrophy type 1 (DM1 or Steinert disease),
an autosomal dominant multisystem disorder caused by a (CTG) n expansion in DMPK gene …

Chaque âge de la vie présente ses spécificités: le fonctionnement psychique n'y échappe
pas. Du nourrisson au sujet âgé, la psychopathologie ne peut se comprendre en fonction …

Not much is known about the neurocognitive deficits in the childhood phenotypic expression
of DM1. Twenty-four children and adolescents with no mental retardation were administered …

Abstract Myotonic dystrophy type 1 (DM1) is the most frequent inherited neuromuscular
disorder. The juvenile form has been associated with cognitive and psychiatric dysfunction …

Abstract Introduction/Aims There is clear evidence for brain involvement in childhood
myotonic dystrophy type 1 (DM1) from imaging studies and the prevalence of intellectual …

Introduction Despite the increased prevalence of comorbid attention deficit hyperactivity
disorder (ADHD) in children with myotonic dystrophy type 1, the effects of methylphenidate …

Background Cognitive impairments in patients with myotonic dystrophy type 1 (DM1) have
often been described, however, there are only few studies differentiating between partial …

Myotonic syndromes (MS) include two main groups of diseases characterized by myotonia
and a variable degree of myopathy: congenital myotonias (CM) and myotonic dystrophies …

Résumé Les maladies neuromusculaires ont longtemps été considérées comme des
pathologies du système nerveux périphérique, pourtant de nombreuses études ont suggéré …