Carine I. van Capelle

A Randomized Study of Alglucosidase Alfa in Late-Onset Pompe's Disease

Ans T. van der Ploeg, Paula R. Clemens, Deyanira Corzo et al. · New England Journal of Medicine · 2010 · 726 citations · Full text

Rate of progression and predictive factors for pulmonary outcome in children and adults with Pompe disease

Nadine A. M. E. van der Beek, Carine I. van Capelle, K.I. van der Velden-van Etten et al. · Molecular Genetics and Metabolism · 2011 · 99 citations

Pompe Disease, Epidemiology, Advanced Lung Disease +9

Eight years experience with enzyme replacement therapy in two children and one adult with Pompe disease

Carine I. van Capelle, Léon P. F. Winkel, M.L.C. Hagemans et al. · Neuromuscular Disorders · 2008 · 98 citations

Pompe Disease, Enzyme Replacement Therapy, Inherited Metabolic Disease +3

Facial‐muscle weakness, speech disorders and dysphagia are common in patients with classic infantile Pompe disease treated with enzyme therapy

Carin M. Van Gelder, Carine I. van Capelle, Berendine J. Ebbink et al. · Journal of Inherited Metabolic Disease · 2011 · 89 citations · Full text

Enzyme Therapy, Motor Development, Otorhinolaryngology +27

Childhood Pompe disease: clinical spectrum and genotype in 31 patients

Carine I. van Capelle, Jan C. van der Meijden, Johanna M. P. van den Hout et al. · Orphanet Journal of Rare Diseases · 2016 · 63 citations · Full text