Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Kroos, M.A."'
Autor:
Ausems, M.G.E.M., Berg, K. ten, Kroos, M.A., van Diggelen, O.P., Wevers, R.A., Poorthuis, B.J.H.M., Niezen-Koning, K.E., van der Ploeg, A.T., Beemer, F.A., Reuser, A.J.J., Sandkuijl, L.A., Wokke, J.H.J.
Publikováno v:
Community Genetics, 1999 Jan 01. 2(2/3), 91-96.
Externí odkaz:
https://www.jstor.org/stable/26664451
Autor:
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.
Publikováno v:
In Journal of the Neurological Sciences 15 December 2008 275(1-2):46-50
Autor:
Ausems, M.G.E.M., Kroos, M.A., Kraan, M. van der, Smeitink, J.A.M., Kleijer, W.J., Ploos van Amstel, J.K., Reuser, A.J.J.
Publikováno v:
Clinical Genetics, 49, 325-328
Clinical Genetics, 49, pp. 325-328
Clinical Genetics, 49, 6, pp. 325-328
Clinical Genetics, 49, pp. 325-328
Clinical Genetics, 49, 6, pp. 325-328
Contains fulltext : 24033___.PDF (Publisher’s version ) (Open Access)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::725aebcaf03dac51d737992fa69946db
https://hdl.handle.net/2066/24033
https://hdl.handle.net/2066/24033
Autor:
Jongen, S.P., Gerwig, G.J., Leeflang, B.R., Koles, K., Mannesse, M.L.M, van Berkel, P.H.C., Pieper, F.R., Kroos, M.A., Reuser, A.J.J., Zhou, Q., Jin, X., Zhang, K., Edmunds, T., Kamerling, J.P.
Pompe disease is a lysosomal glycogen storage disorder characterized by acid α-glucosidase (GAA) deficiency. More than 110 different pathogenic mutations in the gene encoding GAA have been observed. Patients with this disease are being treated by in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______101::2a9834564bd98931a716069017789bef
https://dspace.library.uu.nl/handle/1874/27471
https://dspace.library.uu.nl/handle/1874/27471
Autor:
Kroos, M.A., Kraan, M. van der, Diggelen, O.P. van, Kleijer, W.J., Reuser, A.J.J., Boogaard, M.J. van den, Ausems, M.G.E.M., Ploos van Amstel, J.K., Poenaru, L., Nicolino, M., Wevers, R.A.
Publikováno v:
Journal of Medical Genetics, 32, pp. 836-837
Journal of Medical Genetics, 32, 836-837
Journal of Medical Genetics, 32, 836-837
Item does not contain fulltext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::38c52676d035fee3d066a83993415ceb
https://hdl.handle.net/2066/188466
https://hdl.handle.net/2066/188466
Autor:
de Vries, J.M., Kuperus, E., Hoogeveen-Westerveld, M., Wens, S.C.A., Kroos, M.A., Kruijshaar, M.E., van Doorn, P.A., van der Ploeg, A.T., Pijnappel, W.W.M.
Publikováno v:
In Neuromuscular Disorders October 2014 24(9-10):870-870
Autor:
Nilsson, M.I.1, Kroos, M.A.2, Reuser, A.J.2,3, Hatcher, E.1, Akhtar, M.1, McCready, M.E.4, Tarnopolsky, M.A.1 tarnopol@mcmaster.ca
Publikováno v:
Gene. Mar2014, Vol. 537 Issue 1, p41-45. 5p.
Autor:
Ausems, M.G.E.M., ten Berg, K., Kroos, M.A., van Diggelen, O.P., Wevers, R.A., Poorthuis, B.J.H.M., Niezen-Koning, K.E., van der Ploeg, A.T., Beemer, F.A., Reuser, A.J.J., Sandkuijl, L.A., Wokke, J.H.J.
Publikováno v:
Community Genetics; 2000, Vol. 2 Issue 2/3, p91-96, 6p
Autor:
de Vries, J.M., Brugma, J.C., Ozkan, L., Kroos, M.A., Steegers, E.A.P., Reuser, A.J.J., van Doorn, P.A., van der Ploeg, A.T.
Publikováno v:
In Neuromuscular Disorders October 2011 21(9-10):716-716
Publikováno v:
In Neuromuscular Disorders October 2011 21(9-10):699-699