Background: Myotonic dystrophy type 1 (Steinert’s disease or DM1), the most common form of autosomal dominant muscular dystrophy in adults, is a multisystem disorder, affecting skeletal muscle as well as eyes, heart, gastrointestinal tract, endocrine system, and central nervous system, finally responsible of increasing disabilities and secondary social consequences. To date, DM1-related brain involvement represents a challenging field of research. It is well known that DM1 patients frequently present neuropsychological disturbances and psychiatric comorbidities among which reduced awareness of disease burden and its progression, also defined as anosognosia, is common in clinical practice, this leading to secondary misattribution of symptom...
Myotonic Dystrophy (DM) is a progressive multi-systemic disorder characterized by myotonia and muscl...
Purpose of review Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that affe...
Purpose of review Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that aff...
Background: Myotonic dystrophy type 1 (Steinert's disease or DM1), the most common form of autosomal...
Objective: The objective of this cross-sectional, observational study was to investigate the dise...
Myotonic dystrophy type 1 (DM1) is a dominantly inherited, multisystem condition, arising from patho...
Lack of insight or unawareness of disease could be a typical feature in myotonic dystrophy type 1 (D...
Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy worldwide with complex, mult...
Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy worldwide with complex, mult...
Objective: The goal of the study was to identify brain and functional features associated with prema...
Aims The cognitive profile of Myotonic Dystrophy type 1 (DM1) has been described in recent decade...
AbstractMyotonic dystrophy type 1 (DM1) has a wide phenotypic spectrum and potentially may affect ce...
Myotonic dystrophy type 1 (DM1) has a wide phenotypic spectrum and potentially may affect central ne...
Myotonic dystrophy type-1 (DM1) is a genetic multi-systemic disorder involving several organs includ...
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) represent the most frequent multisystemic muscular ...
Myotonic Dystrophy (DM) is a progressive multi-systemic disorder characterized by myotonia and muscl...
Purpose of review Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that affe...
Purpose of review Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that aff...
Background: Myotonic dystrophy type 1 (Steinert's disease or DM1), the most common form of autosomal...
Objective: The objective of this cross-sectional, observational study was to investigate the dise...
Myotonic dystrophy type 1 (DM1) is a dominantly inherited, multisystem condition, arising from patho...
Lack of insight or unawareness of disease could be a typical feature in myotonic dystrophy type 1 (D...
Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy worldwide with complex, mult...
Myotonic dystrophy type 1 (DM1) is the most frequent muscular dystrophy worldwide with complex, mult...
Objective: The goal of the study was to identify brain and functional features associated with prema...
Aims The cognitive profile of Myotonic Dystrophy type 1 (DM1) has been described in recent decade...
AbstractMyotonic dystrophy type 1 (DM1) has a wide phenotypic spectrum and potentially may affect ce...
Myotonic dystrophy type 1 (DM1) has a wide phenotypic spectrum and potentially may affect central ne...
Myotonic dystrophy type-1 (DM1) is a genetic multi-systemic disorder involving several organs includ...
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) represent the most frequent multisystemic muscular ...
Myotonic Dystrophy (DM) is a progressive multi-systemic disorder characterized by myotonia and muscl...
Purpose of review Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that affe...
Purpose of review Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that aff...