Introduction:In Duchenne muscular dystrophy (DMD) muscle is replaced by adipose tissue. The role of dietary intake (DI) in DMD has not been evaluated. We examined body composition , BMI and adequacy of DI in patients with DMD and evaluated the influence of DI on body composition.Methods:Patients (n=101; age 3 to 18 years; BMI 11.8 to 29.5 kg/m2) completed a dietary recall to determine DI and underwent dual‐energy x‐ray absorptiometry to determine body composition.Results:Preschool‐age and school‐age boys with DMD had high total energy intake. Protein intake/kg exceeded recommendations. As age increased, the percentage of boys with abnormal BMI and fat mass increased, while lean mass decreased. Dietary intake did not predict body fat or lean...
The purpose of this study is to determine the influence of the fat mass percentage and age on the mo...
The skeletal muscles in Duchenne muscular dystrophy and the mdx mouse model lack functional dystroph...
The skeletal muscles in Duchenne muscular dystrophy and the mdx mouse model lack functional dystroph...
Objective: To investigate the relationship between resting energy expenditure (REE) and body composi...
An abnormal nutritional state is often found in Duchenne muscular dystrophy: 54% of dystrophic child...
Duchenne muscular dystrophy (DMD) is the most common and the most severe of the neuromuscular disord...
Duchenne muscular dystrophy (DMD) is a recessive X linked genetic disorder characterised by progress...
Neuromuscular diseases (NMDs) represent a heterogeneous group of acquired or inherited conditions. N...
We aimed to investigate BMI-z course in patients with Duchenne muscular dystrophy (DMD) during trans...
PurposeMuscular dystrophy (MD) is an umbrella term for muscle wasting conditions, for which longitud...
The aim of this study is to investigate the relationship between body composition, anthropometry, an...
hosted at online.sagepub.com Invited Review Duchenne muscular dystrophy (DMD) is a recessive X-linke...
Purpose: Muscular dystrophy (MD) is an umbrella term for muscle wasting conditions, for which longit...
The purpose of this study is to determine the influence of the fat mass percentage and age on the mo...
The aim of this study was to propose a quantitative MR protocol with very short acquisition time and...
The purpose of this study is to determine the influence of the fat mass percentage and age on the mo...
The skeletal muscles in Duchenne muscular dystrophy and the mdx mouse model lack functional dystroph...
The skeletal muscles in Duchenne muscular dystrophy and the mdx mouse model lack functional dystroph...
Objective: To investigate the relationship between resting energy expenditure (REE) and body composi...
An abnormal nutritional state is often found in Duchenne muscular dystrophy: 54% of dystrophic child...
Duchenne muscular dystrophy (DMD) is the most common and the most severe of the neuromuscular disord...
Duchenne muscular dystrophy (DMD) is a recessive X linked genetic disorder characterised by progress...
Neuromuscular diseases (NMDs) represent a heterogeneous group of acquired or inherited conditions. N...
We aimed to investigate BMI-z course in patients with Duchenne muscular dystrophy (DMD) during trans...
PurposeMuscular dystrophy (MD) is an umbrella term for muscle wasting conditions, for which longitud...
The aim of this study is to investigate the relationship between body composition, anthropometry, an...
hosted at online.sagepub.com Invited Review Duchenne muscular dystrophy (DMD) is a recessive X-linke...
Purpose: Muscular dystrophy (MD) is an umbrella term for muscle wasting conditions, for which longit...
The purpose of this study is to determine the influence of the fat mass percentage and age on the mo...
The aim of this study was to propose a quantitative MR protocol with very short acquisition time and...
The purpose of this study is to determine the influence of the fat mass percentage and age on the mo...
The skeletal muscles in Duchenne muscular dystrophy and the mdx mouse model lack functional dystroph...
The skeletal muscles in Duchenne muscular dystrophy and the mdx mouse model lack functional dystroph...