Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Jean Louis Kerkhoffs"'
Autor:
Eva R. Smit, Diana Muñoz Sandoval, Iris C. Kreft, Pieter F. van der Meer, Carmen van der Zwaan, Jan Voorberg, Paula F. Ypma, Arie J. Hoogendijk, Jean-Louis Kerkhoffs, Maartje van den Biggelaar
Publikováno v:
Translational Medicine Communications, Vol 9, Iss 1, Pp 1-12 (2024)
Abstract Background Bone marrow aplasia is a common feature in acute myeloid leukemia (AML) patients during their remission induction treatment, and is associated with potential complications such as bleeding, infection and anemia. Frequent platelet
Externí odkaz:
https://doaj.org/article/aba982d46f2c4cabb3f670f869e6df7c
Autor:
Annelies van Vuren, Jean Louis Kerkhoffs, Saskia Schols, Anita Rijneveld, Erfan Nur, Dore Peereboom, Yves Gandon, Paco Welsing, Richard van Wijk, Roger Schutgens, Wouter van Solinge, Joannes Marx, Tim Leiner, Bart Biemond, Eduard van Beers
Publikováno v:
American Journal of Hematology, 97, 924-932
American Journal of Hematology, 97(7), 924-932. Wiley-Liss Inc.
van Vuren, A, Kerkhoffs, J L, Schols, S, Rijneveld, A, Nur, E, Peereboom, D, Gandon, Y, Welsing, P, van Wijk, R, Schutgens, R, van Solinge, W, Marx, J, Leiner, T, Biemond, B & van Beers, E 2022, ' Proton pump inhibition for secondary hemochromatosis in hereditary anemia : a phase III placebo-controlled randomized cross-over clinical trial ', American Journal of Hematology, vol. 97, no. 7, pp. 924-932 . https://doi.org/10.1002/ajh.26581
American journal of hematology, 97(7), 924-932. Wiley-Liss Inc.
American Journal of Hematology, 97, 7, pp. 924-932
American Journal of Hematology, 97(7), 924-932. Wiley-Liss Inc.
van Vuren, A, Kerkhoffs, J L, Schols, S, Rijneveld, A, Nur, E, Peereboom, D, Gandon, Y, Welsing, P, van Wijk, R, Schutgens, R, van Solinge, W, Marx, J, Leiner, T, Biemond, B & van Beers, E 2022, ' Proton pump inhibition for secondary hemochromatosis in hereditary anemia : a phase III placebo-controlled randomized cross-over clinical trial ', American Journal of Hematology, vol. 97, no. 7, pp. 924-932 . https://doi.org/10.1002/ajh.26581
American journal of hematology, 97(7), 924-932. Wiley-Liss Inc.
American Journal of Hematology, 97, 7, pp. 924-932
Contains fulltext : 251634.pdf (Publisher’s version ) (Open Access) Iron overload is a severe general complication of hereditary anemias. Treatment with iron chelators is hampered by important side-effects, high costs, and the lack of availability
Autor:
Paul, Franck, Petra, Buijs, Annemarie, Meenhuis, Martijn, Dane, Cobie, Postma, Anja, Spaans, Niegel, Gijsbertha, Frans A, Kuypers, Cisca, Hudig, Jean Louis, Kerkhoffs
Publikováno v:
European Journal of Haematology. 108:413-422
Validation of the measurement of erythrocyte deformability as a useful prognostic, rheological biomarker for patients with sickle cell disease (SCD).The degree of reduced deformability was based on the value of the maximum elongation index (EIIn this
Autor:
Elisabeth Dovern, Mesire Aydin, Man Wai Tang, Liesbeth E.M. Suijk, Gerianne M. Hoogendoorn, Charlotte F.J. Van Tuijn, Jean-Louis Kerkhoffs, Caroline E. Rutten, Sacha S. Zeerleder, Mette D. Hazenberg, Bart J. Biemond, Erfan Nur
Publikováno v:
Blood. 140:10476-10477
Autor:
Fabienne M.A. van Hout, Camila Caram-Deelder, Aad Pors, Rutger A. Middelburg, Peter M.J. Rosseel, Leo M.G. van de Watering, Jean-Louis Kerkhoffs, Meindert Palmen, Johanna G. van der Bom
Publikováno v:
SSRN Electronic Journal.
Autor:
Rebecca Cardigan, Helen V. New, Lise Estcourt, Eugene Zhiburt, Rounak Dubey, Jesper Bengtsson, Magnus Jöud, Carlos Castillo, Joan Cid, Miquel Lozano, Dhana Gounder, Peter Flanagan, Sarah Morley, Gwen Clarke, Dana Devine, Salwa Hindawi, Aqeel AlOtaibi, Carolina Bonnet Bub, Jose Mauro Kutner, Toshiyuki Ikeda, Naoko Goto, Hitoshi Okazaki, Magali J. Fontaine, Jeremiah Pasion, Linda Song, Tom Latham, Jean‐Louis Kerkhoffs, Masja Haas, Jaap Jan Zwaginga, Birgit S. Gathof, Katharina Ommer, France Pirenne, Michel Raba, Anne Francois, James Daly, Tanya Powley, Nancy Dunbar
Publikováno v:
Vox Sanguinis, 117(1), E1-E20. WILEY
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa8fffde27205ce5079f781823708adf
https://hdl.handle.net/1887/3566475
https://hdl.handle.net/1887/3566475
Autor:
Rebecca Cardigan, Helen V. New, Lise Estcourt, Eugene Zhiburt, Rounak Dubey, Jesper Bengtsson, Magnus Jöud, Carlos Castillo, Joan Cid, Miquel Lozano, Dhana Gounder, Peter Flanagan, Sarah Morley, Gwen Clarke, Dana Devine, Salwa Hindawi, Aqeel AlOtaibi, Carolina Bonnet Bub, Jose Mauro Kutner, Toshiyuki Ikeda, Naoko Goto, Hitoshi Okazaki, Magali J. Fontaine, Jeremiah Pasion, Linda Song, Tom Latham, Jean‐Louis Kerkhoffs, Masja Haas, Jaap Jan Zwaginga, Birgit S. Gathof, Katharina Ommer, France Pirenne, Michel Raba, Anne Francois, James Daly, Tanya Powley, Nancy Dunbar
Publikováno v:
Vox Sanguinis, 117(1), 136-144. WILEY
Autor:
Johanna C. Wiersum-Osselton, Fabienne M A van Hout, Pieter F van der Meer, Jean-Louis Kerkhoffs, Rutger A. Middelburg, Martin R. Schipperus, Johanna G. van der Bom, Aad Pors
Publikováno v:
Transfusion, 59(10), 3140-3145. WILEY
Background Reports on the clinical consequences of longer storage time of platelet concentrates are contradictory. The objective of this study was to assess whether longer storage times are associated with a higher risk of transfusion reactions. Stud
Autor:
Fabienne M A, van Hout, Pieter F, van der Meer, Johanna C, Wiersum-Osselton, Rutger A, Middelburg, Martin R, Schipperus, Johanna G, van der Bom, Jean-Louis, Kerkhoffs
Publikováno v:
Transfusion. 58(4)
Platelets (PLTs) stored in PLT additive solution (PAS) are associated with fewer allergic reactions than plasma-stored PLTs. However, earlier studies could not provide conclusive evidence on febrile reactions and did not analyze other transfusion rea
Publikováno v:
Cephalalgia. 31:1325-1328
Background: The clinical manifestations of sickle cell disease (SCD) vary, but may be attributed to vaso-occlusion, chronic hemolytic anemia, and infections as a result of functional asplenia. We report a case of a man who presented with severe heada