Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Xandra W. van den Tweel"'
Autor:
Xandra W. van den Tweel, Janneke Hatzmann, Elske Ensink, Johanna H. van der Lee, Marjolein Peters, Karin Fijnvandraat, Martha Grootenhuis
Publikováno v:
Haematologica, Vol 93, Iss 4 (2008)
Caring for a child with sickle cell disease poses extra demands on parents, both practically and psychologically, which may influence their quality of life. Since families of children with sickle cell disease in the Netherlands usually belong to immi
Externí odkaz:
https://doaj.org/article/a790673d21f043c1a2dbe359948a2246
Autor:
Adam J. Tulling, Gertjan Lugthart, Miriam G. Mooij, Caroline L.H. Brackel, Suzanne WJ Terheggen-Lagro, Rianne Oostenbrink, Corinne M.P. Buysse, Simone Hashimoto, Leontien B. van der Aa, Koen J. van Aerde, Wineke Armbrust, Bettina Auffarth-Smedema, Michiel A.G.E. Bannier, Ingeborg Y. Bart, Cherise Beek, Gitanjali I. Bechan, Jolita Bekhof, Merlijn J. van den Berg, Venje H. Boonstra, Mijke Breukels, Danielle M.C. Brinkman, Patricia Bruijning-Verhagen, Stephanie C. de Crom, Margot R. Ernst-Kruis, Pieter L. A. Fraaij, Helma B. van Gameren-Oosterom, Joyce Goris, Michael Groeneweg, Mariken Gruppen, Sanne C. Hammer, Han Hendriks, Petra C.E. Hissink Muller, Jenneke Homan-van der Veen, Marlies A. van Houten, Monique A.M. Jacobs, Lindy Janssen, Arvid W.A. Kamps, Naomi Ketharanathan, Jan W. van der Linden, Kevin H. van 't Kruys, Martijn van der Kuip, Taco Kuijpers, Ankie Lebon, Elizabeth G. Legger, Shirley Lo-A-Njoe, Meindert E. Manshande, Carien J. Miedema, Charlie C. Obihara, Lonneke van Onzenoort-Bokken, Annemarie Oudshoorn, Esther J.E. Peeters, Ronald Petru, Marielle Pijnenburg, Denise Rook, Kim Schilleman, Rian Schopmeijer, David Slotboom, Manouk van der Steen, Kim Stol, Yolande E.M. Thomasse, Wim Tissing, Gerdien A. Tramper-Stranders, Xandra W. van den Tweel, Sebastiaan J. Vastert, Mirjam van Veen, Anne B. Verbeek, Annette M.M. Vernooij-van Langen, Jantien W. Wieringa, Joanne G. Wildenbeest, Saskia N. de Wildt, Christiaan van Woerden, Erik G.J. von Asmuth, Emilie P. Buddingh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc30e8e5798ab70689e624da6d8780ed
https://doi.org/10.2139/ssrn.4401713
https://doi.org/10.2139/ssrn.4401713
Autor:
Daphne Peeters, Jeroen G. Noordzij, Xandra W van den Tweel, Anja Aph Vaessen-Verberne, Gertjan J. Driessen, Pieter Verhulst
Publikováno v:
Pediatric Infectious Disease Journal, 40(11), E424-E426. LIPPINCOTT WILLIAMS & WILKINS
No underlying pathology could be detected in 64% of 208 children presenting with recurrent respiratory tract infections in general pediatric practice. Asthma/preschool wheezing and adenoid hypertrophy were commonly diagnosed. None of the children had
Autor:
Marjolein Peters, Xandra W. van den Tweel, Johanna H. van der Lee, Karin Fijnvandraat, E.F.A. Ensink, Janneke Hatzmann, Martha A. Grootenhuis
Publikováno v:
Haematologica, 93(4), 588-593. Ferrata Storti Foundation
Caring for a child with sickle cell disease poses extra demands on parents, both practically and psychologically, which may influence their quality of life. Since families of children with sickle cell disease in the Netherlands usually belong to immi
Autor:
Evelyn M, van der Plas, Xandra W, van den Tweel, Ronald B, Geskus, Harriët, Heijboer, Bart J, Biemond, Marjolein, Peters, Karin, Fijnvandraat
Publikováno v:
British journal of haematology. 155(1)
This study analyzed the mortality and causes of death in sickle cell disease patients in the Netherlands, to provide a baseline for monitoring the effect of the recently introduced neonatal screening programme and to indicate areas of improvement in
Autor:
Xandra W. van den Tweel, Aart J. Nederveen, Charles B. L. M. Majoie, Johanna H. van der Lee, Laetitia Wagener-Schimmel, Marianne A. A. van Walderveen, Bwee Tien Poll The, Paul J. Nederkoorn, Harriët Heijboer, Karin Fijnvandraat
Publikováno v:
Stroke; a journal of cerebral circulation, 40(3), 795-800. Lippincott Williams and Wilkins
Background and Purpose— Cerebral infarction is an important complication of sickle cell disease (SCD) and occurs in one third of the patients with SCD. The risk of infarction is commonly attributed to the hyperemia that is associated with anemia an
Publikováno v:
European journal of pediatrics, 165(8), 581-582. Springer Verlag
Autor:
Marjolein Peters, Evelyn M. van der Plas, Harriët Heijboer, Bart J. Biemond, Xandra W. van den Tweel, Karin Fijnvandraat, Ronald B. Geskus
Publikováno v:
Blood. 114:1519-1519
Abstract 1519 Poster Board I-542 Introduction Despite the increasing incidence of sickle cell disease (SCD) in the Netherlands, mortality among this patient group has never been investigated. Studies on mortality in patients with SCD from the USA dem
Autor:
Xandra W. van den Tweel, Aart J. Nederveen, Charles B.L.M. Majoie, Johanna H. van der Lee, Laetitia Wagener-Schimmel, Marianne A.A. Walderveen, Bwee Tien Poll The, Paul J. Nederkoorn, Harriet Heijboer, Karin Fijnvandraat
Publikováno v:
Blood. 112:711-711
One of the most devastating complications of SCD is cerebral infarction. Cerebral infarcts are present on MRI scans in one third of SCD patients at the age of 18 years, although most of them are not accompanied by overt, focal neurological deficits.
Autor:
Johanna H. van der Lee, Karin Fijnvandraat, Intr by Marinus H J Van Oers, Xandra W. van den Tweel, Jo Howard
Publikováno v:
Blood. 110:2250-2250
Background: The clinical picture in sickle cell disease (SCD) is highly heterogeneous. Knowledge of the determinants of a severe disease course will help us to unravel the pathophysiological mechanisms underlying the disease process and provide novel