Long-term enzyme-replacement therapy (ERT) with alglucosidase alfa: Evolution of two siblings with juvenile late-onset Pompe disease

6533b7d6fe1ef96bd1266df1

RESEARCH PRODUCT

Long-term enzyme-replacement therapy (ERT) with alglucosidase alfa: Evolution of two siblings with juvenile late-onset Pompe disease

J. Rafael Bretón Martínez Andrés Cánovas Martínez

subject

medicine.medical_specialty business.industry Late onset Enzyme replacement therapy Disease medicine.disease Gastroenterology Neurology Alpha-Glucosidases Internal medicine Glycogen storage disease type II medicine Juvenile Neurology (clinical)business Alglucosidase alfa medicine.drug

year	journal	country	edition	language
2015-11-01	Journal of the Neurological Sciences

https://doi.org/10.1016/j.jns.2015.08.007

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