Zobrazeno 1 - 10
of 147
pro vyhledávání: '"Edward E S Nieuwenhuis"'
Autor:
Wim J E Tissing, Marta Fiocco, Erik Koomen, Edward E S Nieuwenhuis, Marijn Soeteman, Teus H Kappen, Martine van Engelen, Ellen Kilsdonk, Marry van den Heuvel-Eibrink, Roelie M Wösten-van Asperen
Publikováno v:
BMJ Open, Vol 11, Iss 5 (2021)
Introduction Hospitalised paediatric oncology patients are at risk to develop acute complications. Early identification of clinical deterioration enabling adequate escalation of care remains challenging. Various Paediatric Early Warning Systems (PEWS
Externí odkaz:
https://doaj.org/article/ddc35323985942e8a2cfa6766d0b6db3
Autor:
Maartje C M Schouten, Henk F van Stel, Theo J M Verheij, Michiel L Houben, Ingrid M B Russel, Edward E S Nieuwenhuis, Elise M van de Putte
Publikováno v:
PLoS ONE, Vol 12, Iss 1, p e0165641 (2017)
OBJECTIVESTo assess the diagnostic value of the screening instrument SPUTOVAMO-R2 (checklist, 5 questions) for child abuse at Out-of-hours Primary Care locations (OPC), by comparing the test outcome with information from Child Protection Services (CP
Externí odkaz:
https://doaj.org/article/6a78b0653d90487282cced5f7f3f81df
Autor:
Michal Mokry, Magdalena Harakalova, Folkert W Asselbergs, Paul I W de Bakker, Edward E S Nieuwenhuis
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0165893 (2016)
Overlap between non-coding DNA regulatory sequences and common variant associations can help to identify specific cell and tissue types that are relevant for particular diseases. In a systematic manner, we analyzed variants from 94 genome-wide associ
Externí odkaz:
https://doaj.org/article/13fc812ac4dc4e3cafe558b32c2c290e
Autor:
Pieter P E van Lierop, Sigrid M Swagemakers, Charlotte I de Bie, Sabine Middendorp, Peter van Baarlen, Janneke N Samsom, Wilfred F J van Ijcken, Johanna C Escher, Peter J van der Spek, Edward E S Nieuwenhuis
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e79549 (2013)
ObjectiveIn current clinical practice, optimal treatment of inflammatory bowel disease (IBD) aims at the induction and maintenance of clinical remission. Clinical remission is apparent when laboratory markers of inflammation are normal and clinical s
Externí odkaz:
https://doaj.org/article/efa5ee04a5654b7d8d2d142109cfe77b
Autor:
Marijn Soeteman, Marta F. Fiocco, Joppe Nijman, Casper W. Bollen, Maartje M. Marcelis, Ellen Kilsdonk, Edward E. S. Nieuwenhuis, Teus H. Kappen, Wim J. E. Tissing, Roelie M. Wösten-van Asperen
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
BackgroundPediatric oncology patients who require admission to the pediatric intensive care unit (PICU) have worse outcomes compared to their non-cancer peers. Although multi-organ dysfunction (MOD) plays a pivotal role in PICU mortality and morbidit
Externí odkaz:
https://doaj.org/article/4f9b94ffaea945c980a602c45ca07029
Autor:
Jonathan R. A. deWilde, Birgit vanDooijeweert, Annelies J. vanVuren, Elise J. Huisman, Frans J. Smiers, Arian vander Veer, Richard vanWijk, Wouter W. vanSolinge, Edward E. S. Nieuwenhuis, Eduard J. vanBeers, Marije Bartels
Publikováno v:
eJHaem, Vol 3, Iss 4, Pp 1300-1304 (2022)
Abstract In Diamond‐Blackfan anaemia (DBA), iron overload (IO) is common in transfusion‐dependent patients, yet has also been reported in non‐transfusion‐dependent patients. We explored the incidence of IO in transfusion‐dependent and non
Externí odkaz:
https://doaj.org/article/a0c5ad6edef541d88a40c32d271f45fa
Autor:
Marloes Stam, Camiel A Wijngaarde, Bart Bartels, Fay-Lynn Asselman, Louise A M Otto, Laura E Habets, Ruben P A van Eijk, Bas M Middelkoop, H Stephan Goedee, Janke F de Groot, Kit C B Roes, Marja A G C Schoenmakers, Edward E S Nieuwenhuis, Inge Cuppen, Leonard H van den Berg, Renske I Wadman, W Ludo van der Pol
Publikováno v:
Brain Communications, 5
Brain Communications, 5, 1
Brain Communications, 5, 1
Hereditary proximal spinal muscular atrophy causes weakness and increased fatigability of repetitive motor functions. The neuromuscular junction is anatomically and functionally abnormal in patients with spinal muscular atrophy. Pharmacological impro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21143b70317859320feacf01880264ea
http://hdl.handle.net/2066/289329
http://hdl.handle.net/2066/289329
Autor:
Marijn Soeteman, Teus H. Kappen, Martine van Engelen, Maartje Marcelis, Ellen Kilsdonk, Marry M. van den Heuvel‐Eibrink, Edward E. S. Nieuwenhuis, Wim J. E. Tissing, Marta Fiocco, Roelie M. Wösten‐ van Asperen
Publikováno v:
Pediatric Blood and Cancer, 70(1):e30036. Wiley
Pediatric Blood & Cancer, 70(1):e30036. WILEY
Pediatric Blood & Cancer, 70(1):e30036. WILEY
Background: Hospitalized pediatric oncology patients are at risk of severe clinical deterioration. Yet Pediatric Early Warning System (PEWS) scores have not been prospectively validated in these patients. We aimed to determine the predictive performa
Autor:
Arif Ibrahim Ardisasmita, Imre F. Schene, Indi P. Joore, Gautam Kok, Delilah Hendriks, Benedetta Artegiani, Michal Mokry, Edward E. S. Nieuwenhuis, Sabine A. Fuchs
Publikováno v:
Communications Biology. 5
The myriad of available hepatocyte in vitro models provides researchers the possibility to select hepatocyte-like cells (HLCs) for specific research goals. However, direct comparison of hepatocyte models is currently challenging. We systematically se
Autor:
Monique E. Dijsselhof, Tom J. de Koning, Laura A. Tseng, Edward E. S. Nieuwenhuis, Elise A. Ferreira, Rachel Kassel, Margreet van den Born, Holger Rehmann, Sabine A. Fuchs, Gautam Kok, Imre F. Schene, Marie Canton, Suzanne W J Terheggen-Lagro, Arnaud Wiedemann, Joy Dean, Desiree E.C. Smith, Megan Boothe, Clara D.M. van Karnebeek, Gajja Salomons, François Feillet, Marisa I. Mendes
Publikováno v:
Genetics in Medicine
Genetics in medicine, 23(11), 2202-2207. Lippincott Williams and Wilkins
Kok, G, Tseng, L, Schene, I F, Dijsselhof, M E, Salomons, G, Mendes, M I, Smith, D E C, Wiedemann, A, Canton, M, Feillet, F, de Koning, T J, Boothe, M, Dean, J, Kassel, R, Ferreira, E A, van den Born, M, Nieuwenhuis, E E S, Rehmann, H, Terheggen-Lagro, S W J, van Karnebeek, C D M & Fuchs, S A 2021, ' Treatment of ARS deficiencies with specific amino acids ', Genetics in Medicine, vol. 23, no. 11, pp. 2202-2207 . https://doi.org/10.1038/s41436-021-01249-z
Genetics in Medicine, 23(11), 2202-2207. Lippincott Williams and Wilkins
Genetics in Medicine, 23(11), 2202-2207. Nature Publishing Group
Genetics in medicine, 23(11), 2202-2207. Lippincott Williams and Wilkins
Kok, G, Tseng, L, Schene, I F, Dijsselhof, M E, Salomons, G, Mendes, M I, Smith, D E C, Wiedemann, A, Canton, M, Feillet, F, de Koning, T J, Boothe, M, Dean, J, Kassel, R, Ferreira, E A, van den Born, M, Nieuwenhuis, E E S, Rehmann, H, Terheggen-Lagro, S W J, van Karnebeek, C D M & Fuchs, S A 2021, ' Treatment of ARS deficiencies with specific amino acids ', Genetics in Medicine, vol. 23, no. 11, pp. 2202-2207 . https://doi.org/10.1038/s41436-021-01249-z
Genetics in Medicine, 23(11), 2202-2207. Lippincott Williams and Wilkins
Genetics in Medicine, 23(11), 2202-2207. Nature Publishing Group
Purpose: Recessive cytosolic aminoacyl-tRNA synthetase (ARS) deficiencies are severe multiorgan diseases, with limited treatment options. By loading transfer RNAs (tRNAs) with their cognate amino acids, ARS are essential for protein translation. Howe