Objective: To determine the survival in a population of German patients with Duchenne muscular dystrophy. Patients and methods: Information about 94 patients born between 1970 and 1980 was obtained by telephone interviews and questionnaires. In addition to age of death or actual age during the investigation, data concerning clinical course and medical interventions were collected. Results: 67 patients with molecularly confirmed diagnoses had a median survival of 24.0 years. Patients without molecular confirmation (clinical diagnosis only) had a chance of 67 % to reach that age. Grouping of our patient cohort according to the year of death (before and after 2000), ventilation was recognized as main intervention affecting survival with v...
Background: Recent short-term clinical trials in patients with Duchenne Muscular Dystrophy (DMD) hav...
Background: Recent short-term clinical trials in patients with Duchenne Muscular Dystrophy (DMD) hav...
Objectives: To assess life expectancy and cardiovascular mortality in carriers of Duchenne and Becke...
Duchenne Muscular Dystrophy (DMD) is the most common muscle disease in children. Historically, DMD r...
We reviewed the notes of 197 patients with Duchenne muscular dystrophy whose treatment was managed a...
We reviewed the notes of 197 patients with Duchenne muscular dystrophy whose treatment was managed a...
Background: Duchenne muscular dystrophy (DMD) is a progressive muscle disease. No curative therapy i...
BACKGROUND: Duchenne muscular dystrophy (DMD) leads to progressive impairment of muscle function, re...
Background: Duchenne muscular dystrophy (DMD) is a progressive muscle disease. No curative therapy i...
Background: Duchenne muscular dystrophy (DMD) is a progressive muscle disease. No curative therapy i...
Objective: Duchenne Muscular Dystrophy (DMD) is a rare progressive disease, which is often diagnosed...
OBJECTIVE: To find out which patients with Duchenne muscular dystrophy are eligible for starting hom...
OBJECTIVE: To find out which patients with Duchenne muscular dystrophy are eligible for starting hom...
BACKGROUND: Recent short-term clinical trials in patients with Duchenne Muscular Dystrophy (DMD) ha...
OBJECTIVE: To find out which patients with Duchenne muscular dystrophy are eligible for starting hom...
Background: Recent short-term clinical trials in patients with Duchenne Muscular Dystrophy (DMD) hav...
Background: Recent short-term clinical trials in patients with Duchenne Muscular Dystrophy (DMD) hav...
Objectives: To assess life expectancy and cardiovascular mortality in carriers of Duchenne and Becke...
Duchenne Muscular Dystrophy (DMD) is the most common muscle disease in children. Historically, DMD r...
We reviewed the notes of 197 patients with Duchenne muscular dystrophy whose treatment was managed a...
We reviewed the notes of 197 patients with Duchenne muscular dystrophy whose treatment was managed a...
Background: Duchenne muscular dystrophy (DMD) is a progressive muscle disease. No curative therapy i...
BACKGROUND: Duchenne muscular dystrophy (DMD) leads to progressive impairment of muscle function, re...
Background: Duchenne muscular dystrophy (DMD) is a progressive muscle disease. No curative therapy i...
Background: Duchenne muscular dystrophy (DMD) is a progressive muscle disease. No curative therapy i...
Objective: Duchenne Muscular Dystrophy (DMD) is a rare progressive disease, which is often diagnosed...
OBJECTIVE: To find out which patients with Duchenne muscular dystrophy are eligible for starting hom...
OBJECTIVE: To find out which patients with Duchenne muscular dystrophy are eligible for starting hom...
BACKGROUND: Recent short-term clinical trials in patients with Duchenne Muscular Dystrophy (DMD) ha...
OBJECTIVE: To find out which patients with Duchenne muscular dystrophy are eligible for starting hom...
Background: Recent short-term clinical trials in patients with Duchenne Muscular Dystrophy (DMD) hav...
Background: Recent short-term clinical trials in patients with Duchenne Muscular Dystrophy (DMD) hav...
Objectives: To assess life expectancy and cardiovascular mortality in carriers of Duchenne and Becke...