<div><p>Objectives</p><p>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 3T MRI and correlated clinical and neuocognitive symptoms with brain volumetry and voxel-based morphometry (VBM).</p><p>Methods</p><p>12 patients with juvenile or classical DM1 and 16 adult DM2 patients underwent 3T MRI, a thorough neurological and neuropsychological examination and scoring of depression and daytime sleepiness. Volumes of brain, ventricles, cerebellum, brainstem, cervical cord, lesion load and VBM results of the patient groups were compared to 33 matched healthy subjects.</p><p>Results</p><p>Clinical symptoms were depression (more pronounced...
Myotonic dystrophy type 1 (DM1) is a dominantly inherited, multisystem condition, arising from patho...
It is unknown whether brain affection in myotonic dystrophy type 1 (DM1) and 2 (DM2) is due to neuro...
Background Myotonic dystrophy type 1 (DM1) represents a multisystemic disorder in which diffuse brai...
\(\textbf {Objectives:}\) Central nervous system involvement is one important clinical aspect of my...
[eng] OBJECTIVE: Myotonic dystrophy type 1 (DM1), the most prevalent inherited neuromuscular disease...
Myotonic dystrophy type 1 (DM1) has a wide phenotypic spectrum and potentially may affect central ne...
AbstractMyotonic dystrophy type 1 (DM1) has a wide phenotypic spectrum and potentially may affect ce...
<div><p>Objective</p><p>To investigate grey (GM) and white matter (WM) abnormalities and their effec...
Brain involvement in myotonic dystrophy type 1 (DM1) is characterised by cortical atrophy and white ...
The objective of this study was to determine the degree of brain involvement in a cohort of myotonic...
ObjectivesThe aim of this study was to examine the natural history of brain involvement in adult-ons...
ObjectivesThe aim of this study was to examine the natural history of brain involvement in adult-ons...
The variable phenotypic spectrum of myotonic dystrophy type 1 (DM1) includes central nervous system ...
AbstractBackgroundMyotonic dystrophy type 1 (DM1) represents a multisystemic disorder in which diffu...
Myotonic dystrophy type 1 (DM1) is a dominantly inherited, multisystem condition, arising from patho...
It is unknown whether brain affection in myotonic dystrophy type 1 (DM1) and 2 (DM2) is due to neuro...
Background Myotonic dystrophy type 1 (DM1) represents a multisystemic disorder in which diffuse brai...
\(\textbf {Objectives:}\) Central nervous system involvement is one important clinical aspect of my...
[eng] OBJECTIVE: Myotonic dystrophy type 1 (DM1), the most prevalent inherited neuromuscular disease...
Myotonic dystrophy type 1 (DM1) has a wide phenotypic spectrum and potentially may affect central ne...
AbstractMyotonic dystrophy type 1 (DM1) has a wide phenotypic spectrum and potentially may affect ce...
<div><p>Objective</p><p>To investigate grey (GM) and white matter (WM) abnormalities and their effec...
Brain involvement in myotonic dystrophy type 1 (DM1) is characterised by cortical atrophy and white ...
The objective of this study was to determine the degree of brain involvement in a cohort of myotonic...
ObjectivesThe aim of this study was to examine the natural history of brain involvement in adult-ons...
ObjectivesThe aim of this study was to examine the natural history of brain involvement in adult-ons...
The variable phenotypic spectrum of myotonic dystrophy type 1 (DM1) includes central nervous system ...
AbstractBackgroundMyotonic dystrophy type 1 (DM1) represents a multisystemic disorder in which diffu...
Myotonic dystrophy type 1 (DM1) is a dominantly inherited, multisystem condition, arising from patho...
It is unknown whether brain affection in myotonic dystrophy type 1 (DM1) and 2 (DM2) is due to neuro...
Background Myotonic dystrophy type 1 (DM1) represents a multisystemic disorder in which diffuse brai...