Search Results - "Smiers, W"

Parental experiences in end-of-life decision-making in allogeneic pediatric stem cell transplantation: "Have I been a good parent?" by Mekelenkamp, Hilda, Lankester, Arjan C, Bierings, Marc B, Smiers, Frans J W, de Vries, Martine C, Kars, Marijke C

“…In pediatric hematopoietic stem cell transplantation (HSCT), the end-of-life (EOL) phase and the loss of the child is often characterized by a sudden…”
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Treosulfan-induced myalgia in pediatric hematopoietic stem cell transplantation identified by an electronic health record text mining tool by van der Stoep, M. Y. Eileen C., Berghuis, Dagmar, Bredius, Robbert G. M., Buddingh, Emilie P., Mohseny, Alexander B., Smiers, Frans J. W., Guchelaar, Henk-Jan, Lankester, Arjan C., Zwaveling, Juliette

“…Treosulfan is increasingly used as myeloablative agent in conditioning regimen prior to allogeneic hematopoietic stem cell transplantation (HSCT). In our…”
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Usefulness of NGS for Diagnosis of Dominant Beta-Thalassemia and Unstable Hemoglobinopathies in Five Clinical Cases by Rizzuto, Valeria, Koopmann, Tamara T, Blanco-Álvarez, Adoración, Tazón-Vega, Barbara, Idrizovic, Amira, Díaz de Heredia, Cristina, Del Orbe, Rafael, Pampliega, Miriam Vara, Velasco, Pablo, Beneitez, David, Santen, Gijs W E, Waisfisz, Quinten, Elting, Mariet, Smiers, Frans J W, de Pagter, Anne J, Kerkhoffs, Jean-Louis H, Harteveld, Cornelis L, Mañú-Pereira, Maria Del Mar

“…Unstable hemoglobinopathies (UHs) are rare anemia disorders (RADs) characterized by abnormal hemoglobin (Hb) variants with decreased stability. UHs are…”
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Plasma levels of plasminogen activator inhibitor‐1 and bleeding phenotype in patients with von Willebrand disease by Abdul, S., Boender, J., Malfliet, J. J. M. C., Eikenboom, J., Fijn van Draat, K., Mauser‐Bunschoten, E. P., Meijer, K., Meris, J., Laros‐van Gorkom, B. A. P., Bom, J. G., Leebeek, F. W. G., Rijken, D. C., Uitte de Willige, S., Fijnvandraat, K, Coppens, M, Kors, A, Jonkers, H, Boersma, R, Beckers, A, Granzen, B, Tamminga, J, Linden, W, Ypma, F, Smiers, W, Brons, P, Nijziel, M, Cnossen, H

“…Introduction von Willebrand disease (VWD) is the most common inherited bleeding disorder. In VWD patients, large variations in bleeding tendency are observed,…”
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Human Bocavirus in an Immunocompromised Child Presenting with Severe Diarrhea by de Vries, Jutte J.C, Bredius, Robbert G.M, van Rheenen, Patrick F, Smiers, Frans J.W, Schölvinck, Elisabeth H, Vossen, Ann C.T.M, Claas, Eric C.J, Niesters, Hubert G.M

“…Human bocavirus (HBoV) is frequently detected in young children with respiratory symptoms. However, the prevalence and pathogenicity of HBoV in…”
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Successful mismatched hematopoietic stem cell transplantation for pediatric hemoglobinopathy by using ATG and post-transplant cyclophosphamide by Oostenbrink, Lisa V. E., Pool, Emma S., Jol-van der Zijde, Cornelia M., Jansen-Hoogendijk, Anja M., Vervat, Carly, van Halteren, Astrid G. S., Bredius, Robbert G. M., Smiers, Frans J. W., van Tol, Maarten J. D., Schilham, Marco W., Lankester, Arjan C., Mohseny, Alexander B.

“…The use of HLA-mismatched (un)related donors is historically associated with a higher incidence of transplant-related complications and mortality. However, the…”
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Pediatric Bone Marrow Failure: A Broad Landscape in Need of Personalized Management by Vissers, Lotte T W, van der Burg, Mirjam, Lankester, Arjan C, Smiers, Frans J W, Bartels, Marije, Mohseny, Alexander B

“…Irreversible severe bone marrow failure (BMF) is a life-threatening condition in pediatric patients. Most important causes are inherited bone marrow failure…”
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Heterozygous Beta‐Thalassaemia in Pregnancy: Two Rare Causes of Severe Fetal Anemia Requiring Intrauterine Blood Transfusions by van der Meij, Eva, Smiers, Frans J. W., Koopmann, Tamara T., Krapels, Ingrid, LePoole, Kaatje, Lopriore, Enrico, Middeldorp, Johanna M., Ootjers, Claudia S., Scharnhorst, Volkher, Scheepers, Hubertina C. J., Harteveld, Cornelis L., Verweij, E. J. T. (Joanne)

“…ABSTRACT Aim In this article, we present two cases of severe fetal hemolytic anemia based on a beta‐thalassaemia trait inherited from a single parent. Results…”
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Haplo‐identical or mismatched unrelated donor hematopoietic cell transplantation for Fanconi anemia: Results from the Severe Aplastic Anemia Working Party of the EBMT by Zubicaray, Josune, Pagliara, Daria, Sevilla, Julian, Eikema, Dirk‐Jan, Bosman, Paul, Ayas, Mouhab, Zecca, Marco, Yesilipek, Akif, Kansoy, Savas, Renard, Cécile, Dalle, Jean H., Campos, Antonio, Faraci, Maura, Kupesiz, Alphan, Smiers, Frans J. W., Velardi, Andrea, Abecasis, Manuel, Corti, Paola, Fagioli, Franca, González Muñiz, Soledad, Kriván, Gergely, Dufour, Carlo, Risitano, Antonio, Corbacioglu, Selim, Peffault de Latour, Régis

“…Allogeneic hematopoietic cell transplantation (HCT) is the only curative option for bone marrow failure or hematopoietic malignant diseases for Fanconi anemia…”
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Impact of Treosulfan Exposure on Early and Long-Term Clinical Outcomes in Pediatric Allogeneic Hematopoietic Stem Cell Transplantation Recipients: A Prospective Multicenter Study by van der Stoep, M.Y. Eileen C., Bertaina, Alice, Moes, Dirk Jan A.R., Algeri, Mattia, Bredius, Robbert G.M., Smiers, Frans J.W., Berghuis, Dagmar, Buddingh, Emilie P., Mohseny, Alexander B., Guchelaar, Henk-Jan, Locatelli, Franco, Zwaveling, Juliette, Lankester, Arjan C.

“…•In a cohort of pediatric patients who underwent transplantation for nonmalignant diseases, treosulfan exposure was not correlated with 2-year overall survival…”
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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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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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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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Management of cerebral azole-resistant A. fumigatus infection. A role for intraventricular liposomal-amphotericin B? by Schauwvlieghe, A F A D, Bredius, R G M, Verdijk, Rob M, Smiers, Frans J W, van der Beek, Martha T, Goemans, Bianca F, Zwaan, C Michel, Brüggemann, Roger J, Rijnders, Bart J A

“…In the pre-azole era, central nervous system (CNS) infections with Aspergillus had a dismal outcome. Survival improved with voriconazole but CNS infections…”
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Proceeding of the European Group for Blood and Marrow Transplantation (EBMT) congress on sickle cell disease, 16-17 may 2019, Regensburg, Germany: What is the impact of antithymocyte globulin pharmacokinetics on haploidentical hematopoietic stem cell transplantation? by Oostenbrink, Lisa V E, Jol-van der Zijde, Cornelia M, Jansen-Hoogendijk, Anja M, Pool, Emma S, van Halteren, Astrid G S, Moes, Dirk Jan A R, Bredius, Robbert G M, Mohseny, Alex B, Smiers, Frans J W, van Tol, Maarten J D, Schilham, Marco W, Lankester, Arjan C

“…Antithymocyte globulin (ATG) is a widely accepted part of the conditioning regimen applied in the setting of hematopoietic stem cell transplantation (HSCT) to…”
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