Background In this large observational study population of 105 myotonic dystrophy type 1 (DM1) patients, we investigate whether bodyweight is a contributor of total lung capacity (TLC) independent of the impaired inspiratory muscle strength. Methods Body composition was assessed using the combination of body mass index (BMI) and fat-free mass index. Pulmonary function tests and respiratory muscle strength measurements were performed on the same day. Patients were stratified into normal (BMI = 25 kg/m(2)) groups. Multiple linear regression was used to find significant contributors for TLC. Results Overweight was present in 59% of patients, and body composition was abnormal in almost all patients. In overweight patients, TLC was significantly...
To evaluate sensitivity/specificity of the maximum relaxation rate (MRR) of inspiratory muscles, amp...
Duchenne muscular dystrophy (DMD) is characterised by progressive loss of muscular strength that le...
Duchenne muscular dystrophy (DMD) is characterised by progressive loss of muscular strength that lea...
BACKGROUND: In this large observational study population of 105 myotonic dystrophy type 1 (DM1) pati...
In this large observational study population of 105 myotonic dystrophy type 1 (DM1) patients, we inv...
Background Myotonic Dystrophy 1 (DM1) causes progressive myopathy of extremity muscl...
Background: Myotonic dystrophy type 1 (DM1) patients are at risk for metabolic abnormalities and com...
International audienceQuality of life and prognosis of patients with myotonic dystrophy type 1 (MD1)...
Introduction: Respiratory complications are relevant in DM1, leading to a significantly increased mo...
BackgroundDuchenne muscular dystrophy (DMD) is an X-linked recessive disorder associated with progre...
<p>Respiratory function in 105 monotonic dystrophy type 1 (DM1) patients, normal weight (body mass i...
Myotonic dystrophy type 1 (DM1) is one of the most common muscular dystrophies in adults. This revie...
Myotonic dystrophy type 1 (DM1) is one of the most common muscular dystrophies in adults. This revie...
Objective To evaluate sensitivity/specificity of the maximum relaxation rate (MRR) of in...
To evaluate sensitivity/specificity of the maximum relaxation rate (MRR) of inspiratory muscles, amp...
Duchenne muscular dystrophy (DMD) is characterised by progressive loss of muscular strength that le...
Duchenne muscular dystrophy (DMD) is characterised by progressive loss of muscular strength that lea...
BACKGROUND: In this large observational study population of 105 myotonic dystrophy type 1 (DM1) pati...
In this large observational study population of 105 myotonic dystrophy type 1 (DM1) patients, we inv...
Background Myotonic Dystrophy 1 (DM1) causes progressive myopathy of extremity muscl...
Background: Myotonic dystrophy type 1 (DM1) patients are at risk for metabolic abnormalities and com...
International audienceQuality of life and prognosis of patients with myotonic dystrophy type 1 (MD1)...
Introduction: Respiratory complications are relevant in DM1, leading to a significantly increased mo...
BackgroundDuchenne muscular dystrophy (DMD) is an X-linked recessive disorder associated with progre...
<p>Respiratory function in 105 monotonic dystrophy type 1 (DM1) patients, normal weight (body mass i...
Myotonic dystrophy type 1 (DM1) is one of the most common muscular dystrophies in adults. This revie...
Myotonic dystrophy type 1 (DM1) is one of the most common muscular dystrophies in adults. This revie...
Objective To evaluate sensitivity/specificity of the maximum relaxation rate (MRR) of in...
To evaluate sensitivity/specificity of the maximum relaxation rate (MRR) of inspiratory muscles, amp...
Duchenne muscular dystrophy (DMD) is characterised by progressive loss of muscular strength that le...
Duchenne muscular dystrophy (DMD) is characterised by progressive loss of muscular strength that lea...