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6 Most Recent Publications
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Facial-muscle weakness, speech disorders and dysphagia are common in patients with classic infantile Pompe disease treated with enzyme therapy
(Article)
Gelder, C.M. van Capelle, C.I. van Ploeg, A.T. van der Ebbink, B.J. Moor-van Nugteren, I. Hout, J.M.P. van den Hakkesteegt, M.M. Doorn, P.A. van Coo, I.F.M. de Reuser, A.J.J. Gier, H.H.W. de |
2011-10-18
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Low bone mass in Pompe disease. Muscular strength as a predictor of bone mineral density
(Article)
Berg, L.E.M. van den Zandbergen, A.A.M. Capelle, C.I. van Vries, J.M. de Hop, W.C.J. Hout, J.M.P. van den Reuser, A.J.J. Zillikens, M.C. Ploeg, A.T. van der |
2010-09-01
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Reply to the letter to the editor by Papadimas et al.: "Bone mineral density in adult patients with Pompe disease"
(Article)
Berg, L.E.M. van den Zandbergen, A.A.M. Capelle, C.I. van Vries, J.M. de Hop, W.C.J. Hout, J.M.P. van den Reuser, A.J.J. Zillikens, M.C. Ploeg, A.T. van der |
2010-01-01
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Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk
(Article)
Hout, J.M.P. van den Sibbles, B. Corven, E.J. van Hirtum, H. van Kamphoven, J.H.J. Ploeg, A.T. van der Hove, J. van Arts, W.F.M. Doorn, P.A. van Klerk, J.B. de Loonen, M.C.B. Vulto, A.G. Brakenhoff, J.P. Kroos, M.A. Hop, W.C.J. Winkel, L.P.F. Jong, G. de Cromme-Dijkhuis, A.H. Weisglas-Kuperus, N. Reuser, A.J.J. Boer, M. Smeitink, J.A. Diggelen, O.P. van Voort, E. van der |
2004-01-01
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Enzyme Therapy in Infantyle Pompe's Disease: a clinical study of the effects of human alpha-glucosidase produced in the milk of transgenic rabbits
(Doctoral Thesis)
Hout, J.M.P. van den |
2003-09-24
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The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature
(Article)
Hout, J.M.P. van den Ploeg, A.T. van der Hop, W.C.J. Diggelen, O.P. van Smeitink, J.A. Smit, G.P. Poll-The, B.T. Bakker, H.D. Loonen, M.C.B. Klerk, J.B. Reuser, A.J.J. |
2003-01-01
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