textabstractBackground: Pompe disease is a rare metabolic myopathy. In adult patients, progressive weakness of limb-girdle and respiratory muscles often leads to wheelchair and respirator dependency. Clinical studies have shown enzyme replacement therapy (ERT) to positively affect motor and respiratory outcomes. Here we investigate whether ERT reduces patients' risk of needing a wheelchair or respirator. Methods: Data were collected as part of a prospective international survey, the IPA/Erasmus MC Pompe survey, which was conducted annually between 2002 and 2016. We excluded patients who were already using a wheelchair or respirator, those under 18 at survey entry, and those who had missing information. Time-dependent Cox proportional hazard...
BACKGROUND Late-onset Pompe disease (LOPD) is a rare autosomal recessive disorder caused by mutation...
Enzyme replacement therapy (ERT) with recombinant human alglucosidase alfa (rhGAA) in late-onset Pom...
Background: Enzyme replacement therapy (ERT) in adults with Pompe disease, a progressive neuromuscul...
Abstract Background Pompe disease is a rare metabolic myopathy. In adult patients, progressive weakn...
textabstractBackground: Pompe disease is a rare metabolic myopathy for which disease-specific enzyme...
Contains fulltext : 111047.pdf (publisher's version ) (Open Access)ABSTRACT: BACKG...
Background: Pompe disease is an inheritable metabolic disorder for which enzyme replacement therapy ...
International audienceThe efficacy of enzyme replacement therapy (ERT) in patients at an advanced st...
textabstractAbstract. Background: Enzyme replacement therapy (ERT) in adults with Pompe disease, a p...
BACKGROUND AND PURPOSE: Pompe disease is a rare inheritable muscle disorder for which enzyme replace...
textabstractObjectives: Pompe disease is a progressive metabolic myopathy for which enzyme replaceme...
textabstractBackground: Pompe disease is a rare lysosomal storage disorder characterized by muscle w...
PURPOSE: Enzyme replacement therapy (ERT) has been shown to improve outcome in classical infantile P...
Background: Pompe disease, first described in 1932, is a glycogen storage disorder as well as a lyso...
In patients with late-onset Pompe disease (LOPD), the efficacy of the enzyme replacement therapy (ER...
BACKGROUND Late-onset Pompe disease (LOPD) is a rare autosomal recessive disorder caused by mutation...
Enzyme replacement therapy (ERT) with recombinant human alglucosidase alfa (rhGAA) in late-onset Pom...
Background: Enzyme replacement therapy (ERT) in adults with Pompe disease, a progressive neuromuscul...
Abstract Background Pompe disease is a rare metabolic myopathy. In adult patients, progressive weakn...
textabstractBackground: Pompe disease is a rare metabolic myopathy for which disease-specific enzyme...
Contains fulltext : 111047.pdf (publisher's version ) (Open Access)ABSTRACT: BACKG...
Background: Pompe disease is an inheritable metabolic disorder for which enzyme replacement therapy ...
International audienceThe efficacy of enzyme replacement therapy (ERT) in patients at an advanced st...
textabstractAbstract. Background: Enzyme replacement therapy (ERT) in adults with Pompe disease, a p...
BACKGROUND AND PURPOSE: Pompe disease is a rare inheritable muscle disorder for which enzyme replace...
textabstractObjectives: Pompe disease is a progressive metabolic myopathy for which enzyme replaceme...
textabstractBackground: Pompe disease is a rare lysosomal storage disorder characterized by muscle w...
PURPOSE: Enzyme replacement therapy (ERT) has been shown to improve outcome in classical infantile P...
Background: Pompe disease, first described in 1932, is a glycogen storage disorder as well as a lyso...
In patients with late-onset Pompe disease (LOPD), the efficacy of the enzyme replacement therapy (ER...
BACKGROUND Late-onset Pompe disease (LOPD) is a rare autosomal recessive disorder caused by mutation...
Enzyme replacement therapy (ERT) with recombinant human alglucosidase alfa (rhGAA) in late-onset Pom...
Background: Enzyme replacement therapy (ERT) in adults with Pompe disease, a progressive neuromuscul...