Zobrazeno 1 - 10
of 22 637
pro vyhledávání: '"A. T. Van"'
Autor:
A. C. P. Boskma, F. W. Wolthuis, P. D. D. M. Roelofs, A. T. van Wijlen, J. E. van Schie, J. M. de Man- van Ginkel, E. J. Finnema
Publikováno v:
BMC Nursing, Vol 22, Iss 1, Pp 1-10 (2023)
Abstract Background Due to the nursing shortage, positive work environments are needed to retain (student) nurses. More and attractive internships for students need to be ensured. In order to provide more internship places learning departments were d
Externí odkaz:
https://doaj.org/article/4765e7e2ba6747589e457045fe6cf63d
Autor:
I. R. Joosse, V. J. Wirtz, A. T. van Mourik, B. A. Wagner, A. K. Mantel-Teeuwisse, F. Suleman, H. A. van den Ham
Publikováno v:
BMC Health Services Research, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background Sustainable Development Goal (SDG) indicator 3.b.3 monitors progress in medicines’ accessibility for adults and has significant limitations when applying to medicines for children. An adapted indicator methodology was developed
Externí odkaz:
https://doaj.org/article/c1db9a6e7ba740e29baff81e6a8b6c2e
Autor:
G. Ismailova, M. J. Mackenbach, J. M. P. van den Hout, A. T. van der Ploeg, E. Brusse, M. A. E. M. Wagenmakers
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Introduction Patients with Glycogen Storage Disease type II (GSDII), an inheritable metabolic myopathy also known as Pompe disease, are considered to be at risk for severe COVID-19 due to a reduced respiratory function and a tendency to be o
Externí odkaz:
https://doaj.org/article/94c2d99ae37a49daa8f9cd77e9bb8302
Autor:
Heesterbeek, D. G. J., van Riel, M. H. C., van Leeuwen, T., Berg, C. A. T. van den, Sbrizzi, A.
Finding interpretable biomechanical models can provide insight into the functionality of organs with regard to physiology and disease. However, identifying broadly applicable dynamical models for in vivo tissue remains challenging. In this proof of c
Externí odkaz:
http://arxiv.org/abs/2411.06958
Autor:
Olausson, Thomas E., Terpstra, Maarten L., Huttinga, Niek R. F., Beijst, Casper, Blanken, Niels, Correia, Teresa, Suchá, Dominika, Velthuis, Birgitta K., Berg, Cornelis A. T. van den, Sbrizzi, Alessandro
We present a novel approach for the reconstruction of time-resolved free-running first-pass myocardial perfusion MRI, named CMR-MOTUS. This method builds upon the MR-MOTUS framework and addresses the challenges of a contrast varying reference image.
Externí odkaz:
http://arxiv.org/abs/2410.21011
Autor:
J. Schaefers, L. J. van der Giessen, C. Klees, E. H. Jacobs, S. Sieverdink, M. H. G. Dremmen, J. K. H. Spoor, A. T. van der Ploeg, J. M. P. van den Hout, H. H. Huidekoper
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Neuronal ceroid lipofuscinosis type 2 (CLN2 disease) is a rare rapidly progressive neurodegenerative disorder, resulting in early death. Intracerebroventricular enzyme replacement therapy (ERT) with cerliponase alfa is now availab
Externí odkaz:
https://doaj.org/article/8c57c49f00064c658440a8768520074c
Autor:
J. J. A. van den Dorpel, E. Poelman, L. Harlaar, H. A. van Kooten, L. J. van der Giessen, P. A. van Doorn, A. T. van der Ploeg, J. M. P. van den Hout, N. A. M. E. van der Beek
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Enzyme replacement therapy (ERT; alglucosidase alfa) has improved the prospects for patients with classic infantile Pompe disease considerably. However, over time we noticed that many of these children exhibit distal muscle weakne
Externí odkaz:
https://doaj.org/article/271819d21b264ee4ac3cfc5060e9e962
Autor:
E. Poelman, M. Hoogeveen-Westerveld, J. M. P. van den Hout, R. G. M. Bredius, A. C. Lankester, G. J. A. Driessen, S. S. M. Kamphuis, W. W. M. Pijnappel, A. T. van der Ploeg
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Abstract Purpose To evaluate whether immunomodulation can eliminate high sustained antibody levels, and thereby improve clinical outcome in classic infantile Pompe patients receiving enzyme replacement therapy (ERT) with recombinant human alpha-gluco
Externí odkaz:
https://doaj.org/article/5d08294a08ec4d49bfdeb998c62167fc
Autor:
A. T. van der Ploeg, M. Ую Kruijshaar, A. Toscano, P. Laforet, C. Angelini, R. H. Lachmann, S. I. Pascual Pascual, M. Roberts, K. Rosler, T. Stulnig, P. A. van Doorn, P.Y. K. Van den Bergh, J. Vissing, B. Schoser
Publikováno v:
Нервно-мышечные болезни, Vol 8, Iss 4, Pp 19-34 (2019)
Externí odkaz:
https://doaj.org/article/ce2d7bf9e8664d6a848167c86ae07198
Autor:
Liu, Hongyan, Versteeg, Edwin, Fuderer, Miha, van der Heide, Oscar, Schilder, Martin B., Berg, Cornelis A. T. van den, Sbrizzi, Alessandro
Purpose: Current 3D Magnetic Resonance Spin TomogrAphy in Time-domain (MR-STAT) protocols use transient-state, gradient-spoiled gradient-echo sequences that are prone to cerebrospinal fluid (CSF) pulsation artifacts when applied to the brain. This st
Externí odkaz:
http://arxiv.org/abs/2403.15379