European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10‐year experience
Ploeg, A. T., Kruijshaar, M. E., Toscano, A., Laforêt, P., Angelini, C., Lachmann, R. H., Pascual Pascual, S. I., Roberts, M., Rösler, K., Stulnig, T., Doorn, P. A., Van den Bergh, P. Y. K., Vissing, J., Schoser, B., Bembi, Bruno, Broomfield, Alexander, Boentert, Matthias, Desnuelle, Claude, Findling, Oliver, Hahn, Andreas, Díaz‐Manera, Jordi, Hundsberger, Thomas, Kornblum, Cornelia, Labarthé, Franҫois, Laforet, Pascal, Mengel, Karl‐Eugen, Mongini, Tiziana, Muller‐Felber, Wolfgang, Parenti, Giancarlo, Pijnappel, W. Pim, Preisler, Nicolai, Sacconi, Sabrina, Talim, Beril, Tardieu, Marine, Beek, Nadine A.M.E, Wenninger, Stephan
Published in European journal of neurology (01.06.2017)
Published in European journal of neurology (01.06.2017)
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Journal Article
Recommendations for (Discontinuation of) Statin Treatment in Older Adults: Review of Guidelines
Ploeg, Milly A., Floriani, Carmen, Achterberg, Wilco P., Bogaerts, Jonathan M.K., Gussekloo, Jacobijn, Mooijaart, Simon P., Streit, Sven, Poortvliet, Rosalinde K.E., Drewes, Yvonne M.
Published in Journal of the American Geriatrics Society (JAGS) (01.02.2020)
Published in Journal of the American Geriatrics Society (JAGS) (01.02.2020)
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Journal Article
Physical training and high‐protein diet improved muscle strength, parent‐reported fatigue, and physical quality of life in children with Pompe disease
Scheffers, L. E., Somers, O. C., Dulfer, K., Dieleman, G. C., Walet, S., Giessen, L. J., Ploeg, A. T., Hout, J. M. P., Berg, L. E.
Published in Journal of inherited metabolic disease (01.07.2023)
Published in Journal of inherited metabolic disease (01.07.2023)
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Journal Article
Long term survival in patients with classic infantile Pompe disease reveals a spectrum with progressive brain abnormalities and changes in cognitive functioning
Dorpel, J. J. A., Mackenbach, M. J., Dremmen, M. H. G., Vlugt, W. M. C., Rizopoulos, D., Doorn, P. A., Ploeg, A. T., Muetzel, R., Beek, N. A. M. E., Hout, J. M. P.
Published in Journal of inherited metabolic disease (01.07.2024)
Published in Journal of inherited metabolic disease (01.07.2024)
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Journal Article
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
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.
Published in Journal of inherited metabolic disease (01.05.2016)
Published in Journal of inherited metabolic disease (01.05.2016)
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Journal Article
Clinical manifestation and natural course of late-onset Pompe's disease in 54 Dutch patients
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.
Published in Brain (London, England : 1878) (01.03.2005)
Published in Brain (London, England : 1878) (01.03.2005)
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Journal Article
Mild disease course of SARS-CoV-2 infections and mild side effects of vaccination in Pompe disease: a cohort description
Ismailova, G, Mackenbach, M J, van den Hout, J M P, van der Ploeg, A T, Brusse, E, Wagenmakers, M A E M
Published in Orphanet journal of rare diseases (04.03.2022)
Published in Orphanet journal of rare diseases (04.03.2022)
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Journal Article
Effects of immunomodulation in classic infantile Pompe patients with high antibody titers
Poelman, E, Hoogeveen-Westerveld, M, van den Hout, J M P, Bredius, R G M, Lankester, A C, Driessen, G J A, Kamphuis, S S M, Pijnappel, W W M, van der Ploeg, A T
Published in Orphanet journal of rare diseases (22.03.2019)
Published in Orphanet journal of rare diseases (22.03.2019)
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Journal Article
Tomato Mi-gene Resistance-Breaking Populations of Meloidogyne Show Variable Reproduction on Susceptible and Resistant Crop Cultivars
Ploeg, A. T., Stoddard, C. S., Turini, T. A., Nunez, J. J., Miyao, E. M., Subbotin, S. A.
Published in Journal of nematology (01.02.2023)
Published in Journal of nematology (01.02.2023)
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Journal Article
School-based health promotion and physical activity during and after school hours
Vander Ploeg, Kerry A, McGavock, Jonathan, Maximova, Katerina, Veugelers, Paul J
Published in Pediatrics (Evanston) (01.02.2014)
Published in Pediatrics (Evanston) (01.02.2014)
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Journal Article
Presymptomatic treatment of classic late-infantile neuronal ceroid lipofuscinosis with cerliponase alfa
Schaefers, J, van der Giessen, L J, Klees, C, Jacobs, E H, Sieverdink, S, Dremmen, M H G, Spoor, J K H, van der Ploeg, A T, van den Hout, J M P, Huidekoper, H H
Published in Orphanet journal of rare diseases (14.05.2021)
Published in Orphanet journal of rare diseases (14.05.2021)
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Journal Article
Severe tracheal and bronchial collapse in adults with type II mucopolysaccharidosis
Rutten, M, Ciet, P, van den Biggelaar, R, Oussoren, E, Langendonk, J G, van der Ploeg, A T, Langeveld, M
Published in Orphanet journal of rare diseases (26.04.2016)
Published in Orphanet journal of rare diseases (26.04.2016)
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Journal Article
Cognitive outcome of patients with classic infantile Pompe disease receiving enzyme therapy
Ebbink, B J, Aarsen, F K, van Gelder, C M, van den Hout, J M P, Weisglas-Kuperus, N, Jaeken, J, Lequin, M H, Arts, W F M, van der Ploeg, A T
Published in Neurology (08.05.2012)
Published in Neurology (08.05.2012)
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Journal Article
Prognosis in patients with sentinel node-positive melanoma without immediate completion lymph node dissection
van der Ploeg, A. P. T., van Akkooi, A. C. J., Rutkowski, P., Cook, M., Nieweg, O. E., Rossi, C. R., Testori, A., Suciu, S., Verhoef, C., Eggermont, A. M. M.
Published in British journal of surgery (01.10.2012)
Published in British journal of surgery (01.10.2012)
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Journal Article
Distal muscle weakness is a common and early feature in long-term enzyme-treated classic infantile Pompe patients
van den Dorpel, J J A, Poelman, E, Harlaar, L, van Kooten, H A, van der Giessen, L J, van Doorn, P A, van der Ploeg, A T, van den Hout, J M P, van der Beek, N A M E
Published in Orphanet journal of rare diseases (14.09.2020)
Published in Orphanet journal of rare diseases (14.09.2020)
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Journal Article
Facial-muscle weakness, speech disorders and dysphagia are common in patients with classic infantile Pompe disease treated with enzyme therapy
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.
Published in Journal of inherited metabolic disease (01.05.2012)
Published in Journal of inherited metabolic disease (01.05.2012)
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Journal Article
The intellectual disability‐associated CAMK2G p.Arg292Pro mutation acts as a pathogenic gain‐of‐function
Proietti Onori, Martina, Koopal, Balwina, Everman, David B., Worthington, Jessica D., Jones, Julie R., Ploeg, Melissa A., Mientjes, Edwin, Bon, Bregje W., Kleefstra, Tjitske, Schulman, Howard, Kushner, Steven A., Küry, Sébastien, Elgersma, Ype, Woerden, Geeske M.
Published in Human mutation (01.12.2018)
Published in Human mutation (01.12.2018)
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