Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Mieke Aldenhoven"'
Autor:
Natalie I. Mazur, Yvette N. Löwensteyn, Jonne Terstappen, Jeanette Leusen, Fred Schobben, Daniela Cianci, Peter M. van de Ven, Stefan Nierkens, Louis J. Bont, Elisabeth E. Nibbelke, Brigitte Buiteman, Neele Rave, Marlies Vermaas-van Putten, Elly A. Smit-Kleinlugtenbeld, Jacqueline P. de Lege-Korstanje, Marieke G. Peetsold, Anthon Hulsmann, Sandy van Gool, Yvonne Snepvangers, Max Colombijn, Negassi Menelik, Stephanie de Crom, Ben Semmekrot, Wouter J. de Waal, Eline Okhuijsen, Gavin W. ten Tusscher, Ronald A. de Moor, Mijke A. Breukels, Claire Lutterman, Gerdien A. Tramper-Stranders, Johanna H. Oudshoorn, Astrid Ritman, Jeannette S. von Lindern, Gerdina H. Dubbink-Verheij, Maartje M. van den Berg, Marlon E.F. Wilsterman, Edwin Rietveld, Willemijn van Heel, Anne M. de Grauw, Femke Croes, Rienus A. Doedens, Lonneke van Onzenoort-Bokken, Clemens B. Meijssen, Machteld van Scherpenzeel-de Vries, Petra Hoekstra, Linda G.M. van Rooij, Willem-Pieter de Boode, Maaike C. van Rossem, Petra Sipkema, Monique A.M. Jacobs, Marianne A. van Houten, Indrani Kok-Wijesinha, Arine M. Vlieger, Walter Balemans, Frans B. Plötz, Naomi Reijmerink, Stefan M. van Dorth, Willem Heikens, Anke G. Kuijpers, Christel Geesing, Bas J.P. Delsing, Mieke Aldenhoven, Karoly Illy, Eric Hack, Floris Groenendaal, Nicole Derksen, Katrien Oude Rengerink, Jan Meeldijk, Lysette Ebskamp-van Raaij, Jolanda D.F. de Groot-Mijnes, Rob Schuurman
Publikováno v:
EClinicalMedicine, Vol 66, Iss , Pp 102324- (2023)
Summary: Background: Mucosal administration of monoclonal antibodies (mAbs) against respiratory pathogens is a promising alternative for systemic administration because lower doses are required for protection. Clinical development of mucosal mAbs is
Externí odkaz:
https://doaj.org/article/3b10db5a31b4478c974b1456f290efa3
Quality of life of Hurler syndrome patients after successful hematopoietic stem cell transplantation
Autor:
Mieke Aldenhoven, Brigitte T.A. van den Broek, Robert F. Wynn, Anne O'Meara, Paul Veys, Attilio Rovelli, Simon A. Jones, Rossella Parini, Peter M. van Hasselt, Marleen Renard, Victoria Bordon, Tom J. de Koning, Jaap Jan Boelens
Publikováno v:
Blood Advances, Vol 1, Iss 24, Pp 2236-2242 (2017)
Abstract: Hurler syndrome (HS) is a lysosomal storage disease characterized by multisystem morbidity and death in early childhood. Hematopoietic stem cell transplantation (HSCT) results in long-term survival, although with significant residual diseas
Externí odkaz:
https://doaj.org/article/816b9f5cde4c46069c9a97066048c833
Quality of life of Hurler syndrome patients after successful hematopoietic stem cell transplantation
Autor:
Anne O'Meara, Peter M. van Hasselt, Robert Wynn, Marleen Renard, Attilio Rovelli, Simon Jones, Jaap Jan Boelens, Tom J. de Koning, Victoria Bordon, Paul Veys, Mieke Aldenhoven, Rossella Parini, Brigitte T.A. van den Broek
Publikováno v:
Blood Advances, 1(24), 2236. The American Society of Hematology
Blood, 1(24), 2236-2242. AMER SOC HEMATOLOGY
BLOOD ADVANCES
Blood, 1(24), 2236-2242. AMER SOC HEMATOLOGY
BLOOD ADVANCES
Hurler syndrome (HS) is a lysosomal storage disease characterized by multisystem morbidity and death in early childhood. Hematopoietic stem cell transplantation (HSCT) results in long-term survival, although with significant residual disease burden.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fc0feb6dde159c56f0dc0459beb22db
https://dspace.library.uu.nl/handle/1874/359275
https://dspace.library.uu.nl/handle/1874/359275
Autor:
Rossella Parini, Simon Jones, Marleen Renard, Attilio Rovelli, Mieke Aldenhoven, Anne O'Meara, Peter M. van Hasselt, Paul Veys, Victoria Bordon, Jaap-Jan Boelens, Tom J. de Koning, Brigitte T.A. van den Broek, Robert Wynn
Publikováno v:
Biology of Blood and Marrow Transplantation. 24:S29-S30
Publikováno v:
Tijdschrift voor Kindergeneeskunde. 78:88-96
Voor een geselecteerde groep aangeboren stofwisselingsziekten (ASZ) kan een stamceltransplantatie (SCT) de progressie van klinische verschijnselen voorkomen. Dit geldt met name voor specifieke lysosomale stapelingsziekten en peroxisomale stoornissen
Autor:
Monique G.M. de Sain-van der Velden, Frits A. Wijburg, Jaap Jan Boelens, Berthil H.C.M.T. Prinsen, Frans W. Verheijen, Mieke Aldenhoven, Ans T. van der Ploeg, Tom J. de Koning
Publikováno v:
Biology of Blood and Marrow Transplantation, 16, 701-704. Elsevier Inc.
Biology of blood and marrow transplantation, 16(5), 701-704. Elsevier Inc.
Biology of blood and marrow transplantation, 16(5), 701-704. Elsevier Inc.
Hurler syndrome (HS), the most severe phenotype in the spectrum of mucopolysaccharidosis type I, is caused by a deficiency of the lysosomal enzyme alpha-L-iduronidase (IDUA). At present, hematopoietic stem cell transplantation (HSCT) is the only trea
Autor:
Gérard Michel, Anne O'Meara, Maria L. Escolar, Eliane Gluckman, Mieke Aldenhoven, Suhag Parikh, Irina Ionescu, Marina Cavazzana-Calvo, Robert Wynn, Jaap Jan Boelens, Vanderson Rocha, Joanne Kurtzberg, Vinod K. Prasad, Paul Szabolcs
Publikováno v:
Biology of Blood and Marrow Transplantation. 15(5):618-625
Allogeneic stem cell transplantation (SCT) is considered effective in preventing disease progression in patients with Hurler syndrome (HS). Unrelated umbilical cord blood (UCB) grafts are suggested as an alternative to bone marrow (BM) or peripheral
Autor:
Mieke Aldenhoven, Joanne Kurtzberg
Publikováno v:
Cytotherapy, 17(6), 765. Informa Healthcare
Initially used as an alternative hematopoietic stem cell source for patients without a human leukocyte antigen-matched bone marrow or peripheral blood stem cell donor, unrelated cord blood (UCB) is now the preferred donor source when hematopoietic st
Autor:
Peter M. van Hasselt, Ans T. van der Ploeg, Marc Bierings, Robert Wynn, Jean Mercer, Mieke Aldenhoven, Mary Coussons, Simon Jones, Roisin E. Borrill, Denise Bonney, Frits A. Wijburg, Jaap Jan Boelens, Birgitta Versluys
Publikováno v:
Biology of Blood and Marrow Transplantation. 21(2)
Autor:
Maria L. Escolar, Michele D. Poe, Hannah Y. Coletti, Mieke Aldenhoven, Joanne Kurtzberg, Karina Yelin
Publikováno v:
JIMD Reports ISBN: 9783662466995
Hurler syndrome is characterized by progressive multisystem deterioration leading to early death in childhood. This prospective study evaluated the long-term outcomes of patients with Hurler syndrome who underwent umbilical cord blood transplantation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dcd8a4cbb506b499275437995cfe238
https://europepmc.org/articles/PMC4375128/
https://europepmc.org/articles/PMC4375128/