Effects of a higher dose of alglucosidase alfa on ventilator-free survival and motor outcome in classic infantile Pompe disease: an open-label single-center study von van Gelder, C. M., Poelman, E., Plug, I., Hoogeveen-Westerveld, M., van der Beek, N. A. M. E., Reuser, A. J. J., van der Ploeg, A. T.

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Childhood Pompe disease: clinical spectrum and genotype in 31 patients von van Capelle, C I, van der Meijden, J C, van den Hout, J M P, Jaeken, J, Baethmann, M, Voit, T, Kroos, M A, Derks, T G J, Rubio-Gozalbo, M E, Willemsen, M A, Lachmann, R H, Mengel, E, Michelakakis, H, de Jongste, J C, Reuser, A J J, van der Ploeg, A T

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Facial-muscle weakness, speech disorders and dysphagia are common in patients with classic infantile Pompe disease treated with enzyme therapy von van Gelder, C. M., van Capelle, C. I., Ebbink, B. J., Moor-van Nugteren, I., van den Hout, J. M. P., Hakkesteegt, M. M., van Doorn, P. A., de Coo, I. F. M., Reuser, A. J. J., de Gier, H. H. W., van der Ploeg, A. T.

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Clinical manifestation and natural course of late-onset Pompe's disease in 54 Dutch patients von Hagemans, M. L. C., Winkel, L. P. F., Van Doorn, P. A., Hop, W. J. C., Loonen, M. C. B., Reuser, A. J. J., Van der Ploeg, A. T.

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Broad spectrum of Pompe disease in patients with the same c.-32-13T→G haplotype von KROOS, M. A, POMPONIO, R. J, HALLEY, D. J. J, VAN DER PLOEG, A. T, REUSER, A. J. J, HAGEMANS, M. L, KEULEMANS, J. L. M, PHIPPS, M, DERISO, M, PALMER, R. E, AUSEMS, M. G. E. M, VAN DER BEEK, N. A. M. E, VAN DIGGELEN, O. P

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The natural course of non-classic Pompe's disease; a review of 225 published cases von WINKEL, Eon P. F, HAGEMANS, Marloes L. C, VAN DOORN, Pieter A, LOONEN, M. Christa B, HOP ARNOLD, Wim J. C, REUSER, J. J, VAN DER PLOEG, Ans T

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Muscle fiber-type distribution, fiber-type-specific damage, and the Pompe disease phenotype von van den Berg, L. E. M., Drost, M. R., Schaart, G., de Laat, J., van Doorn, P. A., van der Ploeg, A. T., Reuser, A. J. J.

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Cardiac evaluation in children and adults with Pompe disease sharing the common c.−32-13T>G genotype rarely reveals abnormalities von van der Beek, N.A.M.E, Soliman, O.I.I, van Capelle, C.I, Geleijnse, M.L, Vletter, W.B, Kroos, M.A, Reuser, A.J.J, Frohn-Mulder, I.M.E, van Doorn, P.A, van der Ploeg, A.T

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Enzyme therapy for Pompe disease with recombinant human α‐glucosidase from rabbit milk von Van den Hout, J. M. P., Reuser, A. J. J., Klerk, J. B. C., Arts, W. F., Smeitink, J. A. M., Van der Ploeg, A. T.

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Bone, joint and tooth development in mucopolysaccharidoses: Relevance to therapeutic options von Oussoren, E., Brands, M.M.M.G., Ruijter, G.J.G., der Ploeg, A.T. van, Reuser, A.J.J.

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Enzyme analysis for Pompe disease in leukocytes; superior results with natural substrate compared with artificial substrates von van Diggelen, O. P, Oemardien, L. F, van der Beek, N. A. M. E, Kroos, M. A, Wind, H. K, Voznyi, Y. V, Burke, D, Jackson, M, Winchester, B. G, Reuser, A. J. J

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Rate of progression and predictive factors for pulmonary outcome in children and adults with Pompe disease von van der Beek, N.A.M.E., van Capelle, C.I., van der Velden-van Etten, K.I., Hop, W.C.J., van den Berg, B., Reuser, A.J.J., van Doorn, P.A., van der Ploeg, A.T., Stam, H.

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Rate of disease progression during long-term follow-up of patients with late-onset Pompe disease von Van der Beek, N.A.M.E, Hagemans, M.L.C, Reuser, A.J.J, Hop, W.C.J, Van der Ploeg, A.T, Van Doorn, P.A, Wokke, J.H.J

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Inconsistent reporting about dosing, dosing regimen, and immunomodulation therapy in Pompe disease von Reuser, AJJ

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Disease severity in children and adults with Pompe disease related to age and disease duration von HAGEMANS, M. L. C, WINKEL, L. P. F, HOP, W. C. J, REUSER, A. J. J, VAN DOOM, P. A, VAN DER PLOEG, A. T

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Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe disease von BIJVOET, A. G. A, VAN DE KAMP, E. H. M, VAN DER PLOEG, A. T, KROOS, M. A, DING, J.-H, YANG, B. Z, VISSER, P, BAKKER, C. E, VERBEET, M. P, OOSTRA, B. A, REUSER, A. J. J

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Recombinant human α-glucosidase from rabbit milk in Pompe patients von Van den Hout, Hannerieke, Reuser, Arnold JJ, Vulto, Arnold G, Christa B Loonen, M, Cromme-Dijkhuis, Adri, Van der Ploeg, Ans T

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Enzyme therapy in Pompe disease: questions remain von Reuser, A.J.J.

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Eight years experience with enzyme replacement therapy in two children and one adult with Pompe disease von van Capelle, C.I, Winkel, L.P.F, Hagemans, M.L.C, Shapira, S.K, Arts, W.F.M, van Doorn, P.A, Hop, W.C.J, Reuser, A.J.J, van der Ploeg, A.T

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Fatigue : an important feature of late-onset Pompe disease von HAGEMANS, Marloes L. C, VAN SCHIE, Sabine P. M, JANSSENS, A. Cecile J. W, VAN DOORN, Pieter A, REUSER, Arnold J. J, VAN DER PLOEG, Ans T

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