Enzyme replacement therapy has shown to be effective for childhood/adult onset Pompe disease (AOPD). The discovery of biomarkers useful for monitoring disease progression is one of the priority research topics in Pompe disease. Muscle MRI could be one possible test but the correlation between muscle MRI and muscle strength and function has been only partially addressed so far.We studied 34 AOPD patients using functional scales (Manual Research Council scale, hand held myometry, 6 minutes walking test, timed to up and go test, time to climb up and down 4 steps, time to walk 10 meters and Motor Function Measure 20 Scale), respiratory tests (Forced Vital Capacity seated and lying, Maximun Inspiratory Pressure and Maximum Expiratory Pressure), ...
Background: In Pompe disease, an inherited metabolic muscle disorder, severe diaphragmatic weakness ...
Abstract Quantitative muscle MRI is increasingly important in the non-invasive evaluation of neuromu...
Late onset Pompe disease(LOPD) or glycogen storage disease typeⅡis an autosomal recessive disorder c...
Enzyme replacement therapy has shown to be effective for childhood/adult onset Pompe disease (AOPD)....
Late-onset Pompe disease is characterized by progressive weakness involving proximal limb and respir...
Background: Patients with infantile-onset Pompe disease (IOPD) can be identified through newborn scr...
Introduction: The aim of this study was to evaluate the muscle MRI pattern of 9 patients (median age...
Late onset Pompe disease (LOPD) is a slow, progressive disorder characterized by skeletal and respir...
Abstract Adult late-onset Pompe disease is most often a slowly progressive limb-girdle and spine ext...
MRI is a helpful tool for monitoring disease progression in late-onset Pompe disease (LOPD). Our stu...
Pompe disease is a progressive metabolic myopathy. It is caused by a deficiency of the enzyme acid α...
Objectives: Magnetization transfer (MT) imaging exploits the interaction between bulk water protons ...
<p>We observed mild fatty infiltration in muscles of hyperCKemia patients: Tongue (Tin A), paraspina...
Background: Due partly to physicians' unawareness, many adults with Pompe disease are diagnosed with...
Objectives: Pompe disease is a rare genetic disease produced by mutations in the GAA gene leading to...
Background: In Pompe disease, an inherited metabolic muscle disorder, severe diaphragmatic weakness ...
Abstract Quantitative muscle MRI is increasingly important in the non-invasive evaluation of neuromu...
Late onset Pompe disease(LOPD) or glycogen storage disease typeⅡis an autosomal recessive disorder c...
Enzyme replacement therapy has shown to be effective for childhood/adult onset Pompe disease (AOPD)....
Late-onset Pompe disease is characterized by progressive weakness involving proximal limb and respir...
Background: Patients with infantile-onset Pompe disease (IOPD) can be identified through newborn scr...
Introduction: The aim of this study was to evaluate the muscle MRI pattern of 9 patients (median age...
Late onset Pompe disease (LOPD) is a slow, progressive disorder characterized by skeletal and respir...
Abstract Adult late-onset Pompe disease is most often a slowly progressive limb-girdle and spine ext...
MRI is a helpful tool for monitoring disease progression in late-onset Pompe disease (LOPD). Our stu...
Pompe disease is a progressive metabolic myopathy. It is caused by a deficiency of the enzyme acid α...
Objectives: Magnetization transfer (MT) imaging exploits the interaction between bulk water protons ...
<p>We observed mild fatty infiltration in muscles of hyperCKemia patients: Tongue (Tin A), paraspina...
Background: Due partly to physicians' unawareness, many adults with Pompe disease are diagnosed with...
Objectives: Pompe disease is a rare genetic disease produced by mutations in the GAA gene leading to...
Background: In Pompe disease, an inherited metabolic muscle disorder, severe diaphragmatic weakness ...
Abstract Quantitative muscle MRI is increasingly important in the non-invasive evaluation of neuromu...
Late onset Pompe disease(LOPD) or glycogen storage disease typeⅡis an autosomal recessive disorder c...