Background: Late-onset Pompe disease (LOPD) is an autosomal-recessive metabolic myopathy caused by deficiency of the lysosomal enzyme Acid Alpha—Glucosidase (GAA), leading to glycogen accumulation in proximal and axial muscles, and in the diaphragm. Enzyme Replacement Therapy (ERT) with recombinant GAA became available in 2006. Since then, several outcome measures have been investigated for the adequate follow-up of disease progression and treatment response, usually focusing on respiratory and motor function. Prognostic factors predicting outcome have not been identified till now. Methods: In this single Centre, prospective study, we evaluate the response to enzyme replacement therapy in 15 patients (7 males) with LOPD in different stages ...
OBJECTIVE: A multicentre observational study was aimed to assess the prevalence of late-onset Pom...
Pompe disease is a rare inherited metabolic disorder due to the deficiency of the lysosomal enzyme a...
AIMS: Pompe disease is an autosomal recessive lysosomal storage disorder resulting from deficiency ...
Background: Late-onset Pompe disease (LOPD) is an autosomal-recessive metabolic myopathy caused by d...
We reported the long-term follow-up of a population of Late onset Pompe disease treated with enzyme ...
Late onset Pompe disease (LOPD) is a slow, progressive disorder characterized by skeletal and respir...
Objective: To examine respiratory muscle function among late-onset Pompe disease (LOPD) patients in ...
OBJECTIVE The objective of this study was to evaluate a quantitative method based on conventional T...
AIMS: Pompe disease is an autosomal recessive lysosomal storage disorder resulting from deficien...
Background Late-onset Pompe disease (LOPD) is a rare, hereditary, progressive disorder that is usual...
Introduction Late-onset Pompe disease (LOPD) is a progressive metabolic myopathy, affecting skeletal...
Aims: Pompe disease is an autosomal recessive lysosomal storage disorder resulting from deficiency o...
Late onset Pompe disease (LOPD) is characterized by significant motor disabilities, which affect in ...
Background Late-onset Pompe disease is characterized by progressive skeletal myopathy followed by re...
Altres ajuts: This investigation was sponsored by the following grants, one from Sanofi Genzyme and ...
OBJECTIVE: A multicentre observational study was aimed to assess the prevalence of late-onset Pom...
Pompe disease is a rare inherited metabolic disorder due to the deficiency of the lysosomal enzyme a...
AIMS: Pompe disease is an autosomal recessive lysosomal storage disorder resulting from deficiency ...
Background: Late-onset Pompe disease (LOPD) is an autosomal-recessive metabolic myopathy caused by d...
We reported the long-term follow-up of a population of Late onset Pompe disease treated with enzyme ...
Late onset Pompe disease (LOPD) is a slow, progressive disorder characterized by skeletal and respir...
Objective: To examine respiratory muscle function among late-onset Pompe disease (LOPD) patients in ...
OBJECTIVE The objective of this study was to evaluate a quantitative method based on conventional T...
AIMS: Pompe disease is an autosomal recessive lysosomal storage disorder resulting from deficien...
Background Late-onset Pompe disease (LOPD) is a rare, hereditary, progressive disorder that is usual...
Introduction Late-onset Pompe disease (LOPD) is a progressive metabolic myopathy, affecting skeletal...
Aims: Pompe disease is an autosomal recessive lysosomal storage disorder resulting from deficiency o...
Late onset Pompe disease (LOPD) is characterized by significant motor disabilities, which affect in ...
Background Late-onset Pompe disease is characterized by progressive skeletal myopathy followed by re...
Altres ajuts: This investigation was sponsored by the following grants, one from Sanofi Genzyme and ...
OBJECTIVE: A multicentre observational study was aimed to assess the prevalence of late-onset Pom...
Pompe disease is a rare inherited metabolic disorder due to the deficiency of the lysosomal enzyme a...
AIMS: Pompe disease is an autosomal recessive lysosomal storage disorder resulting from deficiency ...