Zobrazeno 1 - 10
of 89
pro vyhledávání: '"J.E. Dankert-Roelse"'
Autor:
A.M.M. Vernooij-van Langen, S.M. van der Pal, A.J.T. Reijntjens, J.G. Loeber, E. Dompeling, J.E. Dankert-Roelse
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 334-344 (2014)
Background: False-positive screening results in newborn screening for cystic fibrosis may lead to parental stress, family relationship problems and a changed perception of the child's health. Aim of the study: To evaluate whether parental anxiety ind
Externí odkaz:
https://doaj.org/article/fb249ebf72fe4e2486d4cc534e32512e
Autor:
Karin M. de Winter-de Groot, Hettie M. Janssens, Johan J.P. Gille, J.E. Dankert-Roelse, Rendelien K. Verschoof-Puite, Bernadette S. Jakobs, Yvonne Schönbeck, Marelle J. Bouva, Vincent Gulmans, Paul H. Verkerk, Peter C. J. I. Schielen
Publikováno v:
Dankert-Roelse, J E, Bouva, M J, Jakobs, B S, Janssens, H M, de Winter-de Groot, K M, Schönbeck, Y, Gille, J J P, Gulmans, V A M, Verschoof-Puite, R K, Schielen, P C J I & Verkerk, P H 2019, ' Newborn blood spot screening for cystic fibrosis with a four-step screening strategy in the Netherlands ', Journal of Cystic Fibrosis, vol. 18, no. 1, pp. 54-63 . https://doi.org/10.1016/j.jcf.2018.07.008
Journal of Cystic Fibrosis, 18, 54-63
Journal of Cystic Fibrosis, 18(1), 54-63. Elsevier
Journal of Cystic Fibrosis, 18, 54-63
Journal of Cystic Fibrosis, 18(1), 54-63. Elsevier
Background: Newborn screening for cystic fibrosis (NBSCF) was introduced in the Dutch NBS program in 2011 with a novel strategy. Methods: Dutch NBSCF consisted of four steps: immuno-reactive trypsin (IRT), Pancreatitis-associated Protein (PAP), DNA a
Akademický článek
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The expansion and performance of national newborn screening programmes for cystic fibrosis in Europe
Autor:
Carlo Castellani, J.E. Dankert-Roelse, Dorota Sands, Sarah Mayell, Simon Pybus, Kevin W Southern, Nataliya Kashirskaya, Barry Linnane, Anne Munck, Silvia Gartner, Victoria Winters, Olaf Sommerburg, Jürg Barben
Publikováno v:
JOURNAL OF CYSTIC FIBROSIS
Background Newborn screening (NBS) for cystic fibrosis (CF) is a well-established public health strategy with international standards. The aim of this study was to provide an update on NBS for CF in Europe and assess performance against the standards
Autor:
Edward Dompeling, Jan-Bart L. Yntema, J.E. Dankert-Roelse, Annette M. M. Vernooij-van Langen, Harm A.W.M. Tiddens, Bert G M Arets, Gerard Loeber
Publikováno v:
European Journal of Pediatrics, 174(8), 1025-1034. Springer, Cham
European Journal of Pediatrics, 174(8), 1025. Springer Verlag
European Journal of Pediatrics, 174(8), 1025-1034. Springer-Verlag
European Journal of Pediatrics, 174(8), 1025. Springer Verlag
European Journal of Pediatrics, 174(8), 1025-1034. Springer-Verlag
After a positive newborn screening test for cystic fibrosis (CF), a sweat test is performed to confirm the diagnosis. The success rate of the generally acknowledged methods (Macroduct/Gibson and Cooke) in newborns varies between 73 and 99 %. The Nano
Autor:
F.L.G.R. Gerzon, J.G. Loeber, Edward Dompeling, J.E. Dankert-Roelse, A.M.M. Vernooij-van Langen
Publikováno v:
Molecular Genetics and Metabolism, 113(1-2), 100-104. Academic Press Inc.
Background: Early diagnosis through newborn screening (NBS) and early treatment of cystic fibrosis (CF) do lead to better prognosis. In the Netherlands, the median age for a clinical diagnosis is six months, and after newborn screening this is 30 day
Publikováno v:
Breathe. :24-30
Educational aims To give an insight into the arguments that have led to the implementation of newborn screening for cystic fibrosis in routine screening programmes. To understand the drawbacks specifically associated with newborn screening for cystic
Publikováno v:
Evidence-Based Child Health: A Cochrane Review Journal. 4:1740-1773
Background Does newborn screening for cystic fibrosis (CF) improve clinical outcomes, quality of life and survival? Objectives To examine whether newborn screening for CF prevents or reduces irreversible organ damage and improves clinical outcomes, q
Autor:
A. F. Nagelkerke, Kevin W Southern, J.E. Dankert-Roelse, Marieke M. E. Mérelle, L. C. M. Kremer, E. C. van Dalen
Publikováno v:
Evidence-Based Child Health: A Cochrane Review Journal. 4:1774-1777
Autor:
Rodney J. Pollitt, Georges Travert, Kevin W Southern, Anne Munck, Luisa Zanolla, Carlo Castellani, J.E. Dankert-Roelse
Publikováno v:
Journal of Cystic Fibrosis. 6:57-65
Background Cystic fibrosis (CF) is a recessively inherited condition caused by mutation of the CFTR gene. Newborn infants with CF have raised levels of immuno-reactive trypsinogen (IRT) in their serum. Measurement of IRT in the first week of life has