Background: In Pompe disease, an inherited metabolic muscle disorder, severe diaphragmatic weakness often occurs. Enzyme replacement treatment is relatively ineffective for respiratory function, possibly because of irreversible damage to the diaphragm early in the disease course. Mildly impaired diaphragmatic function may not be recognized by spirometry, which is commonly used to study respiratory function. In this cross-sectional study, we aimed to identify early signs of diaphragmatic weakness in Pompe patients using chest MRI. Methods: Pompe patients covering the spectrum of disease severity, and sex and age matched healthy controls were prospectively included and studied using spirometry-controlled sagittal MR images of both mid-hemidia...
Pompe disease is an inherited disorder due to a mutation in the gene that encodes acid α-glucosidase...
Enzyme replacement therapy has shown to be effective for childhood/adult onset Pompe disease (AOPD)....
Pompe disease is a progressive metabolic myopathy. It is caused by a deficiency of the enzyme acid α...
Background: In Pompe disease, an inherited metabolic muscle disorder, severe diaphragmatic weakness ...
Background: Pompe disease is a progressive metabolic myopathy. Involvement of respiratory muscles le...
Objectives To evaluate changes in diaphragmatic function in Pompe disease using MRI over time, both ...
The aim of this exploratory study was to evaluate diaphragmatic function across various neuromuscula...
Background: Diaphragm weakness is the main reason for respiratory dysfunction in patients with Pompe...
BACKGROUND: Diaphragm weakness is the main reason for respiratory dysfunction in patients with Pomp...
Objectives: Pompe disease is a rare genetic disease produced by mutations in the GAA gene leading to...
Background Diaphragm weakness is the main reason for respiratory dysfunction in patients with Pompe ...
Pompe disease is a rare autosomal recessive neuromuscular disorder caused by acid α-glucosidase enzy...
PurposeThe diaphragm is the most important muscle of respiration. Disorders of the diaphragm can hav...
Background: Duchenne muscular dystrophy (DMD) is characterized by progressive weakness and wasting o...
Pompe disease is an inherited disorder due to a mutation in the gene that encodes acid α-glucosidase...
Enzyme replacement therapy has shown to be effective for childhood/adult onset Pompe disease (AOPD)....
Pompe disease is a progressive metabolic myopathy. It is caused by a deficiency of the enzyme acid α...
Background: In Pompe disease, an inherited metabolic muscle disorder, severe diaphragmatic weakness ...
Background: Pompe disease is a progressive metabolic myopathy. Involvement of respiratory muscles le...
Objectives To evaluate changes in diaphragmatic function in Pompe disease using MRI over time, both ...
The aim of this exploratory study was to evaluate diaphragmatic function across various neuromuscula...
Background: Diaphragm weakness is the main reason for respiratory dysfunction in patients with Pompe...
BACKGROUND: Diaphragm weakness is the main reason for respiratory dysfunction in patients with Pomp...
Objectives: Pompe disease is a rare genetic disease produced by mutations in the GAA gene leading to...
Background Diaphragm weakness is the main reason for respiratory dysfunction in patients with Pompe ...
Pompe disease is a rare autosomal recessive neuromuscular disorder caused by acid α-glucosidase enzy...
PurposeThe diaphragm is the most important muscle of respiration. Disorders of the diaphragm can hav...
Background: Duchenne muscular dystrophy (DMD) is characterized by progressive weakness and wasting o...
Pompe disease is an inherited disorder due to a mutation in the gene that encodes acid α-glucosidase...
Enzyme replacement therapy has shown to be effective for childhood/adult onset Pompe disease (AOPD)....
Pompe disease is a progressive metabolic myopathy. It is caused by a deficiency of the enzyme acid α...