OBJECTIVE The objective of this study was to evaluate a quantitative method based on conventional T1-weighted magnetic resonance (MR) imaging to assess fatty muscular degeneration in patients with late-onset Pompe disease and to compare it with semi-quantitative visual evaluation (the Mercuri score). In addition, a long-term retrospective data analysis was performed to evaluate treatment response to enzyme replacement therapy with alglucosidase alfa. METHODS MR images of the lumbar spine were acquired in 41 patients diagnosed with late-onset Pompe disease from 2006 through 2015. Two independent readers retrospectively evaluated fatty degeneration of the psoas and paraspinal muscles by applying the Mercuri score. Quantitative semi-automat...
Late-onset Pompe disease is characterized by progressive weakness involving proximal limb and respir...
MRI is a helpful tool for monitoring disease progression in late-onset Pompe disease (LOPD). Our stu...
(1) Background and Purpose: The skeletal muscles of patients suffering from neuromuscular diseases (...
OBJECTIVE: The objective of this study was to evaluate a quantitative method based on conventional ...
Altres ajuts: This investigation was sponsored by the following grants, one from Sanofi Genzyme and ...
Late onset Pompe disease (LOPD) is a slow, progressive disorder characterized by skeletal and respir...
Altres ajuts: Asociación Española de Enfermos de Glucogenosis (AEEG)Quantitative MRI is an increasin...
Background: Late-onset Pompe disease (LOPD) is an autosomal-recessive metabolic myopathy caused by d...
Abstract Adult late-onset Pompe disease is most often a slowly progressive limb-girdle and spine ext...
Altres ajuts: Sanofi GenzymeObjectives: Magnetization transfer (MT) imaging exploits the interaction...
textabstractBackground Late-onset Pompe disease is characterized by progressive skeletal myopathy fo...
Enzyme replacement therapy has shown to be effective for childhood/adult onset Pompe disease (AOPD)....
Objectives: Pompe disease is a rare genetic disease produced by mutations in the GAA gene leading to...
Enzyme replacement therapy has shown to be effective for childhood/adult onset Pompe disease (AOPD)....
Objectives To evaluate changes in diaphragmatic function in Pompe disease using MRI over time, both ...
Late-onset Pompe disease is characterized by progressive weakness involving proximal limb and respir...
MRI is a helpful tool for monitoring disease progression in late-onset Pompe disease (LOPD). Our stu...
(1) Background and Purpose: The skeletal muscles of patients suffering from neuromuscular diseases (...
OBJECTIVE: The objective of this study was to evaluate a quantitative method based on conventional ...
Altres ajuts: This investigation was sponsored by the following grants, one from Sanofi Genzyme and ...
Late onset Pompe disease (LOPD) is a slow, progressive disorder characterized by skeletal and respir...
Altres ajuts: Asociación Española de Enfermos de Glucogenosis (AEEG)Quantitative MRI is an increasin...
Background: Late-onset Pompe disease (LOPD) is an autosomal-recessive metabolic myopathy caused by d...
Abstract Adult late-onset Pompe disease is most often a slowly progressive limb-girdle and spine ext...
Altres ajuts: Sanofi GenzymeObjectives: Magnetization transfer (MT) imaging exploits the interaction...
textabstractBackground Late-onset Pompe disease is characterized by progressive skeletal myopathy fo...
Enzyme replacement therapy has shown to be effective for childhood/adult onset Pompe disease (AOPD)....
Objectives: Pompe disease is a rare genetic disease produced by mutations in the GAA gene leading to...
Enzyme replacement therapy has shown to be effective for childhood/adult onset Pompe disease (AOPD)....
Objectives To evaluate changes in diaphragmatic function in Pompe disease using MRI over time, both ...
Late-onset Pompe disease is characterized by progressive weakness involving proximal limb and respir...
MRI is a helpful tool for monitoring disease progression in late-onset Pompe disease (LOPD). Our stu...
(1) Background and Purpose: The skeletal muscles of patients suffering from neuromuscular diseases (...