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Late-onset Pompe disease (LOPD) in Belgium : clinical characteristics and outcome measures
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The nutritional status in CF : being certain about the uncertainties
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Two successfully completed pregnancies in adult onset Pompe disease, under continued treatment with alglucosidase alfa
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ESPEN-ESPGHAN-ECFS guidelines on nutrition care for infants, children, and adults with cystic fibrosis
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- Journal Article
- A1
- open access
Biomanufacturing of protective antibodies and other therapeutics in edible plant tissues for oral applications
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Long-term outcome of Hurler syndrome patients after hematopoietic cell transplantation : an international multicenter study
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ESPGHAN and NASPGHAN report on the assessment of exocrine pancreatic function and pancreatitis in children
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- Journal Article
- A1
- open access
Belgian consensus on chronic pancreatitis in adults and children : statements on diagnosis and nutritional, medical, and surgical treatment
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Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophy
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Treatment of infants and toddlers with cystic fibrosis-related pancreatic insufficiency and fat malabsorption with pancrelipase MT