Arnold Reuser

Molecular defect in combined beta-galactosidase and neuraminidase deficiency in man.

Alessandra d’Azzo, A. T. Hoogeveen, Arnold Reuser et al. · Proceedings of the National Academy of Sciences · 1982 · 365 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +10

Long-Term Intravenous Treatment of Pompe Disease With Recombinant Human α-Glucosidase From Milk

Johanna M. P. van den Hout, Joep H. J. Kamphoven, Léon P. F. Winkel et al. · PEDIATRICS · 2004 · 354 citations

Life Sciences, Biochemistry, Molecular Medicine +12

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

Coleta Verheij, Cathy Bakker, Esther de Graaff et al. · Nature · 1993 · 340 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Enzyme replacement therapy in late‐onset Pompe's disease: A three‐year follow‐up

Léon P. F. Winkel, Johanna M. P. van den Hout, Joep H. J. Kamphoven et al. · Annals of Neurology · 2004 · 231 citations

Life Sciences, Biochemistry, Enzymology +12

Disease severity in children and adults with Pompe disease related to age and disease duration

M.L.C. Hagemans, Léon P. F. Winkel, Wim C.J. Hop et al. · Neurology · 2005 · 185 citations

Public Health, Child Health, Pediatrics +11