Search Results - "Smiers, F J"

A neonate with spontaneous arterial limb ischemia and an aneurysm of the oval foramen: a case report by van Vonderen, J. J, Keus, J. M. H, van Schaik, J, Smiers, F. J, ten Harkel, D. J, Lopriore, E

“…Background In this case report, we describe a very rare case of severe limb ischemia due to an arterial embolus caused by an aneurysm of the oval foramen in a…”
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Antibodies to anti-thymocyte globulin in aplastic anemia patients have a negative impact on hematopoietic SCT by Jol-van der Zijde, C M, Bredius, R G M, Jansen-Hoogendijk, A M, Smiers, F J, Lankester, A C, van Tol, M J D

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Suppression of Hb Bart's to improve tissue oxygenation and fetal development in homozygous alpha‐thalassemia by Lugthart, G., Verweij, E. J. T., Harteveld, C. L., Tan, R. N. G. B., Knapen, M. F. C. M., Slaghekke, F., Haak, M. C., Mohseny, A. B., Smiers, F. J.

“…Intra‐uterine reduction of Hb Bart's only reached with exchange transfusions…”
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Management and Outcome in 32 Neonates with Thrombotic Events by Walther, Frans J., Lopriore, Enrico, van Elteren, H. A., Sramek, A., Kollen, W. J., Smiers, F. J., Veldt, H. S., te Pas, Arjan B., Roest, Arno A. W.

“…Objective. To determine the incidence, management, complications, and outcome in neonates with thrombotic events. Study Design. We performed a retrospective…”
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Anti-CD20 monoclonal antibody (rituximab) for refractory autoimmune thrombocytopenia in a girl with systemic lupus erythematosus by ten Cate, R., Smiers, F. J., Bredius, R. G. M., Lankester, A. C., van Suijlekom-Smit, L. W. A., Huizinga, T. W., Egeler, R. M.

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Paediatric allogeneic bone marrow transplantation for homozygous β-thalassaemia, the Dutch experience by BALL, L. M, LANKESTER, A. C, GIORDANO, P. C, VAN WEEL, M. H, HARTEVELD, C. L, BREDIUS, R. G. M, SMIERS, F. J, EGELER, R. M, VOSSEN, Jmjj

“…We reviewed the results of the Dutch paediatric bone marrow transplant (BMT) program for children receiving HLA-identical BMT for beta-thalassaemia major over…”
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Management of cerebral azole-resistant Aspergillus fumigatus infection: A role for intraventricular liposomal-amphotericin B by Schauwvlieghe, A.F.A.D., Bredius, R.G.M., Verdijk, R.M., Smiers, F.J.W., van der Beek, M.T., Goemans, B.F., Zwaan, C.M., Brüggemann, R.J., Rijnders, B.J.A.

“…•Azole-resistant aspergillosis is an emerging global problem.•CNS infections with azole-resistant Aspergillus have a dismal outcome.•Three patients were…”
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Impact of von Willebrand disease on health‐related quality of life in a pediatric population by 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.

“…Background: Von Willebrand disease (VWD) is the most frequent inherited bleeding disorder. Whether VWD is associated with health‐related quality of life…”
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Heterogeneity of proliferative responses of human B cell precursor acute lymphoblastic leukemia (BCP-ALL) cells to interleukin 7 (IL-7): no correlation with immunoglobulin gene status and expression of IL-7 receptor or IL-2/IL-4/IL-7 receptor common gamma chain genes by Smiers, F J, van Paassen, M, Pouwels, K, Beishuizen, A, Hählen, K, Löwenberg, B, Touw, I P

“…Interleukin 7 (IL-7) stimulates proliferation of normal human and murine B cell precursor (BCP) cells in a distinct fashion, depending on the stage of…”
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CD20 and CD40 mediated mitogenic responses in B-lineage acute lymphoblastic leukaemia by Smiers, F J, van Paassen, M, Hählen, K, Löwenberg, B, Touw, I P

“…Activation of CD20, a cross-membrane ion channel, induces cell cycle progression from G0 to G1 in B lymphocytes. Subsequent activation of CD40, a membrane…”
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Sickle cell disease: Clinical presentation and management of a global health challenge by Houwing, M.E., de Pagter, P.J., van Beers, E.J., Biemond, B.J., Rettenbacher, E., Rijneveld, A.W., Schols, E.M., Philipsen, J.N.J., Tamminga, R.Y.J., van Draat, K. Fijn, Nur, E., Cnossen, M.H.

“…Sickle cell disease is an autosomal recessive, multisystem disorder, characterised by chronic haemolytic anaemia, painful episodes of vaso-occlusion,…”
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Inhibitor development and mortality in non‐severe hemophilia A by Eckhardt, C. L., Loomans, J. I., Velzen, A. S., Peters, M., Mauser‐Bunschoten, E. P., Schwaab, R., Mazzucconi, M. G., Tagliaferri, A., Siegmund, B., Reitter‐Pfoertner, S. E., Bom, J. G., Fijnvandraat, K., Fijnvandraat, K., Peters, M., Kamphuisen, P. W., Kamphuisen, P. W., Bom, J. G., Peerlinck, K., Oldenburg, J., Santagostino, E., Astermark, J., Eckhardt, C.L, Velzen, A.S, Streefkerk, N., Loomans, J. L., Eijkelenburg, A., Jansen, A. J., Kruijt, C. C., Tienoven, B., Baar, A. C. G., Corten, I. W., Meijer, K., Nijziel, M. R., Dors, N., Hamulyak, K., Beckers, E., Brons, P. P., Laros‐van Gorkom, B. A. P., Heerde, W. L., Leebeek, F., Kruip, M., Cnossen, M. H., Mauser‐Bunschoten, E., Fischer, K., Smiers, F. J., Hermans, C., Schwaab, R., Siegmund, B., Klamroth, R., Escuriola‐Ettingshausen, C., Königs, C., Petrini, P., Holmström, M., Mäkipernaa, A., Male, C., Pabinger, I., Reitter‐Pfoertner, S. E., Keenan, R. D., Liesner, R., Khair, K., Yee, T. T., Hart, D. P., Rangarajan, S., Mitchell, M., Thompson, G., Haya, S., Moret, A., Cid, A. R., Jimenez‐Yuste, V., Mancuso, M. E., Mazzuconni, M. G., Santoro, C., Morfini, M., Castaman, G., Schinco, P., Tagliaferri, A., Rivolta, G. F., Platokouki, H., McRae, S.

“…Summary Background The life expectancy of non‐severe hemophilia A (HA) patients equals the life expectancy of the non‐hemophilic population. However, data on…”
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Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients by Swinkels, Maurice, Atiq, Ferdows, Bürgisser, Petra E., Moort, Iris, Meijer, Karina, Eikenboom, Jeroen, Fijnvandraat, Karin, Galen, Karin P. M., Meris, Joke, Schols, Saskia E. M., Bom, Johanna G., Cnossen, Marjon H., Voorberg, Jan, Leebeek, Frank W. G., Bierings, Ruben, Jansen, A. J. Gerard, Fijnvandraat, K., Coppens, M., Meris, J., Nieuwenhuizen, L., Meijer, K., Tamminga, R. Y. J., Ypma, P. F., Eikenboom, H. C. J., Bom, J. G., Smiers, F. J. W., Granzen, B., Moenen, F., Brons, P., Schols, S. E. M., Leebeek, F. W. G., Cnossen, M. H., Atiq, F., Kwawegen, C. B., Galen, K. P. M.

“…Summary Von Willebrand disease (VWD) is a bleeding disorder caused by quantitative (type 1 or 3) or qualitative (type 2A/2B/2M/2N) defects of circulating von…”
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Back to base pairs: What is the genetic risk for red bloodcell alloimmunization? by Gerritsma, J.J., Oomen, I., Meinderts, S., van der Schoot, C.E., Biemond, B.J., van der Bom, J.G., Fijnvandraat, K., van Beers, E.J., Biemond, B.J., Beijlevelt, M., Brons, P.P.T., Cnossen, M.H., Dovern, L., Fijnvandraat, K., Heijboer, H., Hofstede, F., Kerkhoffs, J.L.H., Nur, E., Ootjers, C., de Pagter, P.J., Rijneveld, A.W., Schols, S.E.M., Smiers, F.J., Suiker, M.H., Teuben, S.A.M.C., van Tuijn, C.F.J., van Vliet, I., Zwagemaker, E.

“…Red blood cell (RBC) alloimmunization is a serious complication of blood transfusions, challenging selection of compatible units for future transfusions…”
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BMI is an important determinant of VWF and FVIII levels and bleeding phenotype in patients with von Willebrand disease by Atiq, Ferdows, Fijnvandraat, Karin, Galen, Karin P. M., Laros‐Van Gorkom, Britta A. P., Meijer, Karina, Meris, Joke, Coppens, Michiel, Mauser‐Bunschoten, Eveline P., Cnossen, Marjon H., Bom, Johanna G., Eikenboom, Jeroen, Leebeek, Frank W. G.

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CLEC4M and STXBP5 gene variations contribute to von Willebrand factor level variation in von Willebrand disease by Sanders, Y. V., Bom, J. G., Isaacs, A., Cnossen, M. H., Maat, M. P. M., Laros‐van Gorkom, B. A. P., Fijnvandraat, K., Meijer, K., Duijn, C. M., Mauser‐Bunschoten, E. P., Eikenboom, J., Leebeek, F. W. G., Coppens, M., Kors, A., Meris, J., Nijziel, M. R., Tamminga, R. Y. J., Ypma, P. F., Smiers, F. J. W., Granzen, B., Hamulyák, K., Brons, P.

“…Summary Background von Willebrand factor (VWF) levels in healthy individuals are influenced by variations in genetic loci other than the VWF gene, whose…”
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Paediatric allogeneic bone marrow transplantation for homozygous -thalassaemia, the Dutch experience by Ball, L M, Lankester, A C, Giordano, P C, van Weel, M H, Harteveld, C L, Bredius, R G M, Smiers, F J, Egeler, R M, J M J J Vossen

“…We reviewed the results of the Dutch paediatric bone marrow transplant (BMT) program for children receiving HLA-identical BMT for beta-thalassaemia major over…”
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Further characterization of the 5'-flanking region of the rat lactase-phlorizin hydrolase gene by Verhave, M, Krasinski, S D, Maas, S M, Smiers, F J, Mishra, K, Breeuwsma, N G, Naim, H Y, Grand, R J

“…The lactase-phlorizin hydrolase gene is widely used as a marker of intestinal differentiation. Recent evidence demonstrating that transcription plays a major…”
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Anti-CD20 monoclonal antibody (rituximab) for refractory autoimmune thrombocytopenia in a girl with systemic lupus erythematosus by ten Cate, R, Smiers, F J, Bredius, R G M, Lankester, A C, van Suijlekom-Smit, L W A, Huizinga, T W, Egeler, R M

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