Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Janneke I. Loomans"'
Autor:
Janneke I. Loomans, Marieke J.H.A. Kruip, Manuel Carcao, Shannon Jackson, Alice S. van Velzen, Marjolein Peters, Elena Santagostino, Helen Platokouki, Erik Beckers, Jan Voorberg, Johanna G. van der Bom, Karin Fijnvandraat, for the RISE consortium
Publikováno v:
Haematologica, Vol 103, Iss 3 (2018)
Desmopressin increases endogenous factor VIII levels in hemophilia A. Large inter-individual variation in the response to desmopressin is observed. Patients with a lower baseline factor VIII activity tend to show a reduced response, therefore, desmop
Externí odkaz:
https://doaj.org/article/acbe979985fc47ecba83394ab98d4cc2
Publikováno v:
Journal of clinical and translational research, 3(Suppl 2), 351-357
Journal of Clinical and Translational Research
Journal of Clinical and Translational Research
Background: The half-life and mean residence time (MRT) of infused recombinant factor VIII (FVIII) concentrate are associated with pre-infusion levels of von Willebrand factor (VWF) in severely affected hemophilia A patients. It is currently unknown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58b1398fef8850114d031b389205260e
https://pure.amc.nl/en/publications/administration-of-ddavp-did-not-improve-the-pharmacokinetics-of-fviii-concentrate-in-a-clinically-significant-manner(edf0fa13-bd60-4d63-942c-2933af43334b).html
https://pure.amc.nl/en/publications/administration-of-ddavp-did-not-improve-the-pharmacokinetics-of-fviii-concentrate-in-a-clinically-significant-manner(edf0fa13-bd60-4d63-942c-2933af43334b).html
Autor:
Natasja Dors, Paul P. T. Brons, J. G. van der Bom, Anne Mäkipernaa, Saturnino Haya, M. Peters, Jan Voorberg, A S van Velzen, M. Holmström, Corien L. Eckhardt, Karin Fijnvandraat, Janneke I. Loomans
Publikováno v:
Journal of Thrombosis and Haemostasis, 15, 246-254
Journal of Thrombosis and Haemostasis, 15(2), 246-254
Journal of thrombosis and haemostasis : JTH
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Journal of thrombosis and haemostasis, 15(2), 246-254. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 15, 2, pp. 246-254
Journal of Thrombosis and Haemostasis, 15(2), 246-254
Journal of thrombosis and haemostasis : JTH
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Journal of thrombosis and haemostasis, 15(2), 246-254. Wiley-Blackwell
Journal of Thrombosis and Haemostasis, 15, 2, pp. 246-254
Contains fulltext : 170609.pdf (Publisher’s version ) (Closed access) Essentials Factor VIII levels vary in mild and moderate hemophilia A (MHA) patients with the same mutation. We aimed to estimate the variation and determinants of factor VIII lev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d4c2189f4edbfae1214b417bc106651
https://doi.org/10.1111/jth.13581
https://doi.org/10.1111/jth.13581
Autor:
Janneke I, Loomans, Janske, Lock, Marjolein, Peters, Frank W G, Leebeek, Marjon H, Cnossen, Karin, Fijnvandraat
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 158
Haemophilia is an X-linked inherited clotting disorder with a prevalence of 1 per 5000 men. A deficiency of clotting factor VIII (FVIII; haemophilia A) or IX (FIX; haemophilia B) causes haemophilia patients to suffer from spontaneous bleeding and exc
Autor:
Karin Fijnvandraat, Corien L. Eckhardt, A.C.G. van Baar, Elena Santagostino, Giancarlo Castaman, Janneke I. Loomans, M. Peters, A S van Velzen, Marieke J. H. A. Kruip
Publikováno v:
Tijdschrift voor Kindergeneeskunde. 81:81-81
s ingediend voor het Amsterdam Kindersymposium 2013 81 RISE: Response to DDAVP In mild Hemophilia A patients: in Search for dEterminants J.I. Loomans (1), A.C.G. van Baar (1), A.S. van Velzen (1), M. Kruip (3), E. Santagostino (4), C.L. Eckhardt (1,2