Search Results - "de Pagter, P.J"

Human herpesvirus type 6 reactivation after haematopoietic stem cell transplantation by de Pagter, P.J, Schuurman, Rob, Meijer, Ellen, van Baarle, Debbie, Sanders, E.A.M, Boelens, J.J

“…Abstract Human herpesvirus type 6 (HHV6) is known to reactivate after hematopoetic stem cell transplantation (HSCT) and has been suggested to be associated…”
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Increased proportion of perforin-expressing CD8+ T-cells indicates control of herpesvirus reactivation in children after stem cell transplantation by de Pagter, P.J, Boelens, J.J, Jacobi, R, Schuurman, R, Nanlohy, N.M, Sanders, E.A.M, van Baarle, D

“…Abstract Hematopoietic stem cell transplantation (HSCT) is frequently complicated by viral reactivations. Early diagnosis of viral reactivations and preemptive…”
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Chromosomally Integrated Human Herpesvirus 6: Transmission via Cord Blood-Derived Unrelated Hematopoietic Stem Cell Transplantation by de Pagter, P.J, Virgili, Anne, Nacheva, Ellie, van Baarle, Debbie, Schuurman, Rob, Boelens, Jaap J

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O.2.8 Human herpes virus 6 reactivation after haematopoietic stem cell transplantation in children: a typing analysis by Keukens, L, de Pagter, P.J, de Vos, N.M, Boelens, J.J, Schuurman, R

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O.6.1 Human Herpesvirus type 6 external quality assessment evaluation among 51 laboratories in Europe by de Pagter, P.J, van Loon, A.M, de Vos, N.M, MacKay, W.G, Pandit, A, Schuurman, R

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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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Human Herpes Virus 6 Plasma DNA Positivity after Hematopoietic Stem Cell Transplantation in Children: an Important Risk Factor for Clinical Outcome by Anne de Pagter, P.J, Schuurman, Rob, Visscher, Henk, de Vos, Machiel, Bierings, Marc, van Loon, Anton M, Uiterwaal, Cuno S.P.M, van Baarle, Debbie, Sanders, Elisabeth A.M, Boelens, JaapJan

“…Abstract Human herpes virus 6 (HHV6) is known to reactivate after hematopoietic stem cell transplantation (HSCT), and has been suggested to be associated with…”
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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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Improving Access to Healthcare for Pediatric Sickle Cell Disease Patients and Their Families by Houwing, Maite E., Buddenbaum, Marit, Verheul, Thijs C.J., de Pagter, Anne P.J., Hazelzet, Jan A, Cnossen, Marjon H.

“…Introduction Sickle cell disease (SCD) is a severe inherited red blood cell disorder with high morbidity requiring integrated comprehensive care. There are not…”
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Long‐term parental distress after pediatric hematopoietic stem cell transplantation for nonmalignant diseases by Bense, Joëll E., Stiggelbout, Anne M., Lankester, Arjan C., de Pagter, Anne P. J.

“…Abstract Background Survival rates have continued to increase for pediatric hematopoietic stem cell transplantation (HSCT) for nonmalignant diseases. Despite…”
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Clonal Hematopoiesis Is Common in Long-Term Survivors of Pediatric Hematopoietic Cell Transplantation, Including Umbilical Cord Blood Transplantation by Müskens, Konradin F., van Bergen, Maaike G.J.M., de Graaf, Aniek O., Wieringa, Nienke, te Pas, Brigit M., Pagter, Anne P.J. de, Bense, Joëll E., Lankester, Arjan C., Kremer, Leontien C.M., Jansen, Joop H., Huls, Geert A., Nierkens, Stefan, Lindemans, Caroline A., Belderbos, Mirjam E.

“…Background 1. Approximately 20.000 to 200.000 hematopoietic stem and progenitor cells (HSPCs) contribute to steady-state adult hematopoiesis. During ageing,…”
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Multicenter External Quality Assessment of Molecular Methods for Detection of Human Herpesvirus 6 by de Pagter, P.J, Schuurman, R, de Vos, N.M, Mackay, W, van Loon, A.M

“…The purpose of this study was to evaluate the performance of laboratories for the detection and quantification of human herpesvirus 6 (HHV-6) by an external…”
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Health Literacy, Self-Efficacy and Knowledge of Sickle Cell Disease Among Caregivers by Houwing, Maite E., Grohssteiner, Rowena, Teuben, Sonja A.M.C., Hazelzet, Jan A, de Pagter, Anne P.J., Fransen, Mirjam P., Cnossen, Marjon H.

“…Introduction Sickle cell disease (SCD) is a hereditary red blood cell disorder characterized by severe anemia, acute and painful vaso-occlusive crises and…”
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The Cost of Healthcare for Pediatric Patients with Sickle Cell Disease by Houwing, Maite E., Thielen, Frederick, Pagter, Anne P.J. de, Hazelzet, Jan A, Blommestein, Hedwig, Uyl-de Groot, Carin A., Cnossen, Marjon H.

“…Introduction Sickle cell disease (SCD) is an autosomally, recessive inherited hemoglobinopathy and multisystem disorder characterized by ongoing hemolytic…”
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Silent Cerebral Infarcts in Sickle Cell Disease: A Systematic Review by Houwing, Maite E., Grohssteiner, Rowena, de Pagter, Anne P.J., Fijnvandraat, Karin, Oosterlaan, Jaap, Haverman, Lotte, Dremmen, Marjolein, White, Tonya, Cnossen, Marjon H.

“…Introduction The most common neurological finding in children and adults with sickle cell disease (SCD) is the presence of silent cerebral infarcts (SCIs)…”
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Late endocrine effects after hematopoietic stem cell transplantation in children with nonmalignant diseases by de Kloet, L. C., Bense, J. E., van der Stoep, M. Y. E. C., Louwerens, M., von Asmuth, E. G. J., Lankester, A. C., de Pagter, A. P. J., Hannema, S. E.

“…The number of children undergoing hematopoietic stem cell transplantation (HSCT) for nonmalignant diseases has increased in recent years. Endocrine…”
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Physician exhaustion and work engagement during the COVID-19 pandemic: A longitudinal survey into the role of resources and support interventions by Solms, Lara, van Vianen, Annelies E M, Koen, Jessie, Kan, Kees-Jan, de Hoog, Matthijs, de Pagter, Anne P J

“…Physicians increasingly show symptoms of burnout due to the high job demands they face, posing a risk for the quality and safety of care. Job and personal…”
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Silent cerebral infarcts in patients with sickle cell disease: a systematic review and meta-analysis by Houwing, Maite E, Grohssteiner, Rowena L, Dremmen, Marjolein H G, Atiq, Ferdows, Bramer, Wichor M, de Pagter, Anne P J, Zwaan, C Michel, White, Tonya J H, Vernooij, Meike W, Cnossen, Marjon H

“…Silent cerebral infarcts (SCIs) are the most common neurological complication in children and adults with sickle cell disease (SCD). In this systematic review,…”
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Turning the tide: a quasi-experimental study on a coaching intervention to reduce burn-out symptoms and foster personal resources among medical residents and specialists in the Netherlands by Solms, Lara, van Vianen, Annelies, Koen, Jessie, Theeboom, Tim, de Pagter, Anne P J, De Hoog, Matthijs

“…ObjectivesPhysician burn-out is increasing, starting already among residents. The consequences of burn-out are not limited to physicians’ well-being, they also…”
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Health‐related quality of life in infants, toddlers and young children with sickle cell disease by Houwing, Maite E., Muntendam, Madieke J., Muilekom, Maud M., Teela, Lorynn, Fijnvandraat, Karin, Pagter, Anne P. J., Heijboer, Henriëtte, Oers, Hedy A., Cnossen, Marjon H., Haverman, Lotte

“…Background Little is known about health‐related quality of life (HRQoL) in young children with sickle cell disease living in a European country. Methods A…”
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