SUMMARY Twenty-nine patients with myotonic dystrophy from 14 families were tested with the Wechsler and Shipley measures of cognitive function. Forty-one per cent of the subjects had little or no physical handicap. Approximately one-third had low Wechsler scores, whereas 7 % had relatively high scores. There was a trend for affected females to have poorer cognitive function than males. Limited cognitive ability correlated with maternal inheritance of the gene and severe physical handicap, but there were individual exceptions. Strongest cognitive abilities were verbal and informational, whereas the weakest were immediate recall, abstraction and spatial manipula-tion and orientation. There was no evidence of intellectual decline with time. Si...
A previous study in proximal myotonic myopathy (PROMM/DM-2) and myotonic dystrophy type 1 (DM-1) usi...
To characterize the progression of the cognitive involvement in patients affected by myotonic dystro...
Background: Myotonic dystrophy (DM) is a genetic multisystemic disease with muscular, endocrine, ocu...
SUMMARY Twenty-nine patients with myotonic dystrophy from 14 families were tested with the Wechsler ...
Cognitive functions were investigated in 37 patients with myotonic dystrophy (MD) and correlated wit...
Background and purpose: Studies on cognitive decline in myotonic dystrophy type 1 (DM1) are characte...
The aim of the present study is to explore whether affective and cognitive social cognition impairme...
To examine the cognitive profile of patients with myotonic dystrophy type 1 (DM1) on the basis of a ...
We evaluated 40 patients suffering from a severe form a myotonic dystrophy (MD) with neuropsychologi...
Duchenne muscular dystrophy and myotonic dystrophy are genetic, progressive muscle diseases. These m...
Twenty-two adults with myotonic dystrophy were assessed for evidence of intellectual impairment and ...
Background: Central nervous system involvement occurs in most patients with myotonic dystrophy type ...
AIMS:The cognitive profile of Myotonic Dystrophy type 1 (DM1) has been described in recent decades. ...
Myotonic dystrophy type 1 (DM1), the most common muscular dystrophy observed in adults, is a genetic...
Twenty-seven patients with myotonic dystrophy (MD) and 20 control subjects were tested using neurops...
A previous study in proximal myotonic myopathy (PROMM/DM-2) and myotonic dystrophy type 1 (DM-1) usi...
To characterize the progression of the cognitive involvement in patients affected by myotonic dystro...
Background: Myotonic dystrophy (DM) is a genetic multisystemic disease with muscular, endocrine, ocu...
SUMMARY Twenty-nine patients with myotonic dystrophy from 14 families were tested with the Wechsler ...
Cognitive functions were investigated in 37 patients with myotonic dystrophy (MD) and correlated wit...
Background and purpose: Studies on cognitive decline in myotonic dystrophy type 1 (DM1) are characte...
The aim of the present study is to explore whether affective and cognitive social cognition impairme...
To examine the cognitive profile of patients with myotonic dystrophy type 1 (DM1) on the basis of a ...
We evaluated 40 patients suffering from a severe form a myotonic dystrophy (MD) with neuropsychologi...
Duchenne muscular dystrophy and myotonic dystrophy are genetic, progressive muscle diseases. These m...
Twenty-two adults with myotonic dystrophy were assessed for evidence of intellectual impairment and ...
Background: Central nervous system involvement occurs in most patients with myotonic dystrophy type ...
AIMS:The cognitive profile of Myotonic Dystrophy type 1 (DM1) has been described in recent decades. ...
Myotonic dystrophy type 1 (DM1), the most common muscular dystrophy observed in adults, is a genetic...
Twenty-seven patients with myotonic dystrophy (MD) and 20 control subjects were tested using neurops...
A previous study in proximal myotonic myopathy (PROMM/DM-2) and myotonic dystrophy type 1 (DM-1) usi...
To characterize the progression of the cognitive involvement in patients affected by myotonic dystro...
Background: Myotonic dystrophy (DM) is a genetic multisystemic disease with muscular, endocrine, ocu...