Search Results - "Cuijpers, Marloes"

HOVON110/ReBeL Study: Results of the Phase I Part of a Randomized Phase I/II Study of Lenalidomide, Rituximab With or Without Bendamustine in Patients With Relapsed/Refractory Follicular Lymphoma by Stevens, Wendy B.C., Bakunina, Katerina, Cuijpers, Marloes, Chamuleau, Martine, Beeker, Aart, Fijnheer, Rob, Hebart, Holger, Visser, Hein P.J., Doorduijn, Jeanette K., Linton, Kim, Dreyling, Martin, Jong, Daphne, Kersten, Marie José

“…Supplemental Digital Content is available in the text…”
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Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9 by Schmitz-Abe, Klaus, Ciesielski, Szymon J., Schmidt, Paul J., Campagna, Dean R., Rahimov, Fedik, Schilke, Brenda A., Cuijpers, Marloes, Rieneck, Klaus, Lausen, Birgitte, Linenberger, Michael L., Sendamarai, Anoop K., Guo, Chaoshe, Hofmann, Inga, Newburger, Peter E., Matthews, Dana, Shimamura, Akiko, Snijders, Pieter J.L.M., Towne, Meghan C., Niemeyer, Charlotte M., Watson, Henry G., Dziegiel, Morten H., Heeney, Matthew M., May, Alison, Bottomley, Sylvia S., Swinkels, Dorine W., Markianos, Kyriacos, Craig, Elizabeth A., Fleming, Mark D.

“…The congenital sideroblastic anemias (CSAs) are relatively uncommon diseases characterized by defects in mitochondrial heme synthesis, iron-sulfur (Fe-S)…”
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Treatment of Steroid Resistant Grade II to IV Acute Gvhd by Infusion of Mesenchymal Stroma Cells Expanded with Human Plasma and Platelet Lysate - a Phase I/II Study by te Boome, Liane CJ, Mansilla, Cristina M, Lindemans, Caroline A, Van der Wagen, Lotte E, Cuijpers, Marloes, Slaper-Cortenbach, Ineke, Rozemuller, Henk, Petersen, Eefke J, Spierings, Eric, Bierings, Marc, Boelens, Jaap J, Wulffraat, Nico, Kuball, Jurgen H

“…Abstract 736 Despite multiple improvements in the last decade in the field of HSCT, acute graft versus host disease (aGVHD) remains a life-threatening…”
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Treatment of Steroid Resistant Grade II to IV Acute GVHD by Infusion of Mesenchymal Stroma Cells Expanded with Platelet Lysate - a Phase I/II Study by te Boome, Liane, Mansilla, Cristina, Lindemans, Caroline, van der Wagen, Lotte, Cuijpers, Marloes, Slaper-Cortenbach, Ineke, Rozemuller, Henk, Petersen, Eefke, Spierings, Eric, Bierings, Marc, Boelens, Jaap-Jan, Wullfraat, Nico, Kuball, Jurgen

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New causes of microcytic anaemia: hereditary disorders of iron homeostasis by van Rooijen, Karlijn L, Raymakers, Reinier A P, Cuijpers, Marloes L H, Brons, Paul P T, Janssen, Mirian C H, Swinkels, Dorine W

“…Recently various new gene defects have been identified which explain some previously unknown causes of inherited microcytic anaemias. These defects are located…”
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Iron deficiency anaemia due to a matriptase-2 mutation by Cuijpers, M L H Marloes, Wiegerinck, Erwin T G, Brouwer, Rick, de Witte, Theo J M, Swinkels, Dorine W

“…A 36-year old female patient who had had iron deficiency anaemia since her childhood showed no clear response to oral iron treatment. Elevated serum hepcidin…”
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