Variation in baseline factor VIII concentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identical F8 mutations

Autor: Loomans, J.I. ^*, van Velzen, A.S., Eckhardt, C.L., Peters, M., Mäkipernaa, A., Holmstrom, M., Brons, P.P., Dors, N., Haya, S., Voorberg, J., van der Bom, J.G., Fijnvandraat, K.

Publikováno v: In Journal of Thrombosis and Haemostasis February 2017 15(2):246-254

Impact of von Willebrand disease on health‐related quality of life in a pediatric population

Autor: DE WEE, E.M., FIJNVANDRAAT, K., DE GOEDE‐BOLDER, A., MAUSER‐BUNSCHOTEN, E.P., EIKENBOOM, J.C.J., BRONS, P.P., SMIERS, F.J., TAMMINGA, R., OOSTENBRINK, R., RAAT, H., VAN DER BOM, J.G., LEEBEEK, F.W.G. ^*

Publikováno v: In Journal of Thrombosis and Haemostasis March 2011 9(3):502-509

Factor VIII gene (F8) mutation and risk of inhibitor development in nonsevere hemophilia A

Autor: Eckhardt, C.L., Velzen, A.S. van, Peters, M., Astermark, J., Brons, P.P., Castaman, G., Cnossen, M.H., Dors, N., Escuriola-Ettingshausen, C., Hamulyak, K., Hart, D.P., Hay, C.R.M., Haya, S., Heerde, W.L. van, Hermans, C., Holmstrom, M., Jimenez-Yuste, V., Keenan, R.D., Klamroth, R., Gorkom, B.A.P., Leebeek, F.W.G., Liesner, R., Makipernaa, A., Male, C., Mauser-Bunschoten, E., Mazzucconi, M.G., Mcrae, S., Meijer, K., Mitchell, M., Morfini, M., Nijziel, M., Oldenburg, J., Peerlinck, K., Petrini, P., Platokouki, H., Reitter-Pfoertner, S.E., Santagostino, E., Schinco, P., Smiers, F.J., Siegmund, B., Tagliaferri, A., Yee, T.T., Kamphuisen, P.W., Bom, J.G. van der, Fijnvandraat, K., INSIGHT Study Grp

Publikováno v: Blood, Vol. 122, no. 11, p. 1954-1962 (2013)
Blood, 122(11), 1954-1962. AMER SOC HEMATOLOGY
Blood
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Blood, 122(11), 1954-1962. The American Society of Hematology
Blood, 122(11), 1954-1962. American Society of Hematology
Blood, 122, 1954-62
Blood, 122, 11, pp. 1954-62
Blood, 122(11), 1954-1962

Neutralizing antibodies (inhibitors) toward factor VIII form a severe complication in nonsevere hemophilia A, profoundly aggravating the bleeding pattern. Identification of high-risk patients is hampered by lack of data that take exposure days to the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::743d96f24835da6cdd8c7ba8de20c1d8
https://doi.org/10.1182/blood-2013-02-483263

School-aged children after the end of successful treatment of non-central nervous system cancer: longitudinal assessment of health-related quality of life, anxiety and coping

Autor: Maurice-Stam, H., Oort, F.J., Last, B.F., Brons, P.P., Caron, H.N., Grootenhuis, M.A.

Publikováno v: Maurice-Stam, H, Oort, F J, Last, B F, Brons, P P, Caron, H N & Grootenhuis, M A 2009, ' School-aged children after the end of successful treatment of non-central nervous system cancer: Longitudinal assessment of health-related quality of life, anxiety and coping ', European Journal of Cancer Care, vol. 18, no. 4, pp. 401-410 . https://doi.org/10.1111/j.1365-2354.2008.01041.x
European Journal of Cancer Care, 18(4), 401-410. Wiley-Blackwell
European journal of cancer care, 18(4), 401-410. Wiley-Blackwell
European Journal of Cancer Care, 18, 401-10
European Journal of Cancer Care, 18, 4, pp. 401-10

Contains fulltext : 81585.pdf (Publisher’s version ) (Closed access) The aim of the study was to investigate: (1) health-related quality of life (HRQoL) and anxiety in school-aged cancer survivors during the first 4 years of continuous remission af

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5751f2322a69f27351fbc9938bb7fad
https://hdl.handle.net/11245/1.318222

Von Willebrand Factor antigen and age explain variation in baseline FVIII:C among nonsevere hemophilia A patients with the same F8 genotype (Arg593Cys and Asn618Ser)

Autor: Loomans, J.I., Velzen, A.S. van, Eckhardt, C.L., Peters, M., Astermark, J., Brons, P.P., Castaman, G., Cnossen, M.H., Dors, N., Escuriola-Ettingshausen, C., Hamulyak, K., Hart, D.P., Hay, C.R.M., Haya, S., Heerde, W.L. van, Hermans, C., Holmstroom, M., Jimenez-Yuste, V., Keenan, R.D., Klamroth, R., Konigs, C., Kruip, M.J.H.A., Laros-Van Gorkom, B.A.P., Leebeek, F.W.G., Liesner, R., Makipernaa, A., Male, C., Mauser-Bunschoten, E., Mazzucconi, M.G., Mcrae, S., Meijer, K., Mitchell, M., Morfini, M., Nijziel, M., Oldenburg, J., Peerlinck, K., Petrini, P., Platokouki, H., Rangarajan, S., Reitter-Pfoertner, S.E., Santagostino, E., Schinco, P., Smiers, F.J., Siegmund, B., Tagliaferri, A., Yee, T.T., Kamphuisen, P.W., Bom, J.G. van der, Fijnvandraat, K., Insight Rise Study Grp

Publikováno v: Haemophilia, 20, 56-56

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::66f2b6ade1925acca356a552e8ca18af
https://hdl.handle.net/1887/107333