Zobrazeno 1 - 10
of 1 150
pro vyhledávání: '"R. van Wijk"'
Autor:
W. C. A. M. van Nieuwburg, B. J. J. van Spreuwel, M. T. K. Tran, M. D. Yang, A. Greidanus, G. Mulder, M. J. Tummers, J. Westerweel, W. Suijker, R. van Wijk
Publikováno v:
Frontiers in Sports and Active Living, Vol 5 (2023)
The principal aim of the work presented here is to investigate and demonstrate that a forward tilted rowing blade would result in a more efficient and effective motion of the blade through the water that would result in a higher boat speed when an eq
Externí odkaz:
https://doaj.org/article/fb4f8c2c8267444aa99581ee1e33b1f9
Autor:
M.J. van Dijk, M.A.E. Rab, B.A. van Oirschot, J.F. Bos, C. Derichs, A.W. Rijneveld, M.H. Cnossen, E. Nur, B.J. Biemond, M. Bartels, J.J.M. Jans, W.W. van Solinge, R.E.G. Schutgens, R. van Wijk, E.J. van Beers
Publikováno v:
HemaSphere, Vol 7, Iss S1, Pp 1-2 (2023)
Externí odkaz:
https://doaj.org/article/bd3ef75f29b54108a2e1002a2243269c
Autor:
M. Rab, C. Kanne, C. Boisson, J. Bos, B. van Oirschot, M. Houwing, C. Renoux, R. Schutgens, M. Bartels, A. Rijneveld, E Nur, M. Cnossen, P. Joly, R. Fort, P. Connes, R. van Wijk, V. Sheehan, E. van Beers
Publikováno v:
HemaSphere, Vol 6, Pp 167-168 (2022)
Externí odkaz:
https://doaj.org/article/d6ea5ea2cb30491cb09c6eefb5cbbb20
P1065: CONGENITAL ERYTHROCYTOSIS DUE TO HETEROZYGOUS VARIANTS IN THE BISPHOSPHOGLYCERATE MUTASE GENE
Autor:
M. J. van Dijk, B. A. van Oirschot, M. C. Stam-Slob, B. van der Zwaag, E. J. van Beers, J. J. Jans, P. van der Linden, J. M. Torregrosa Diaz, B. Gardie, F. Girodon, R. Schots, N. Thielen, R. van Wijk
Publikováno v:
HemaSphere, Vol 6, Pp 955-956 (2022)
Externí odkaz:
https://doaj.org/article/72517628478246cf87fc9a1d00d99ed7
Autor:
A. Idrizovic, A. Collado Gimbert, E. van Beers, R. Colombatti, P. Bartolucci, M. de Montalembert, M. P. Boaro, D. Beneitez, A. Ortuño, A. Ruiz, I. Isola, E. Cela, R. Van Wijk, M. Rab, M. D. M. Mañú Pereira
Publikováno v:
HemaSphere, Vol 6, Pp 1360-1361 (2022)
Externí odkaz:
https://doaj.org/article/6201aa95c21a40c184d6e9896d8109f8
Autor:
M. J. van Dijk, M. A. Rab, B. A. van Oirschot, J. Bos, C. Derichs, A. W. Rijneveld, M. H. Cnossen, E. Nur, B. J. Biemond, M. Bartels, J. J. Jans, W. W. van Solinge, R. E. Schutgens, R. van Wijk, E. J. van Beers
Publikováno v:
HemaSphere, Vol 6, Pp 1382-1383 (2022)
Externí odkaz:
https://doaj.org/article/063dfee7b0054496815fe2b048a8de69
Autor:
S. van der Veen, M. van Dijk, J. Jans, N. Verhoeven-Duif, R. van Wijk, M. Bartels, M. Mañú Pereira, R. Colombatti, M. Martella, V. Munaretto, M. Boaro, P. Bartolucci, M. Cnossen, B. Biemond, E. van Beers
Publikováno v:
HemaSphere, Vol 6, Pp 1381-1382 (2022)
Externí odkaz:
https://doaj.org/article/5093c3c701b14fd2b6b2320a0332ea74
Autor:
A. Van Vuren, J. Kerkhoffs, S. Schols, A. Rijneveld, E. Nur, D. Peereboom, Y. Gandon, P. Welsing, R. van Wijk, R. Schutgens, W. van Solinge, J. Marx, T. Leiner, B. Biemond, E. van Beers
Publikováno v:
HemaSphere, Vol 6, Pp 1447-1448 (2022)
Externí odkaz:
https://doaj.org/article/b0456faf472e4ab6b1a74ce1c0194597
Autor:
M. Rab, M. van Dijk, J. Bos, B. van Oirschot, J. Gerrits, P. Kosinski, C. Kung, J. Jans, E. van Beers, L. Dang, R. van Wijk
Publikováno v:
HemaSphere, Vol 6, Pp 1374-1375 (2022)
Externí odkaz:
https://doaj.org/article/b7de0407c32643a190e95540b074e4f6
Autor:
M. C. Berrevoets, J. Bos, R. Huisjes, T. H. Merkx, B. A. van Oirschot, W. W. van Solinge, J. W. Verweij, M. Y. A. Lindeboom, E. J. van Beers, M. Bartels, R. van Wijk, M. A. E. Rab
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Hereditary spherocytosis (HS) is the most common form of hereditary chronic hemolytic anemia. It is caused by mutations in red blood cell (RBC) membrane and cytoskeletal proteins, which compromise membrane integrity, leading to vesiculation. Eventual
Externí odkaz:
https://doaj.org/article/d0e47726aa1e487ba4c28ffa4ae28c67