The Value of a Checklist for Child Abuse in Out-of-Hours Primary Care: To Screen or Not to Screen.

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

Soluble leukocyte-Associated Ig-like Receptor-1 in amniotic fluid is of fetal origin and positively associates with lung compliance.

Autor: Michiel L Houben, Marloes J M Olde Nordkamp, Peter G J Nikkels, Cornelis K van der Ent, Linde Meyaard, Louis Bont

Publikováno v: PLoS ONE, Vol 8, Iss 12, p e83920 (2013)

The soluble form of the inhibitory immune receptor leukocyte-Associated Ig-like Receptor-1 (sLAIR-1) is present in plasma, urine and synovial fluid and correlates to inflammation. We and others previously showed inflammatory protein expression in nor

Externí odkaz: https://doaj.org/article/504264295cbe4528aac681f2e1c0730e

Executive functioning in preschoolers with 22q11.2 deletion syndrome and the impact of congenital heart defects

Autor: Emma Everaert, Jacob A. S. Vorstman, Iris S. Selten, Martijn G. Slieker, Frank Wijnen, Tessel D. Boerma, Michiel L. Houben

Publikováno v: Journal of Neurodevelopmental Disorders, Vol 15, Iss 1, Pp 1-19 (2023)

Abstract Background Executive functioning (EF) is an umbrella term for various cognitive functions that play a role in monitoring and planning to effectuate goal-directed behavior. The 22q11.2 deletion syndrome (22q11DS), the most common microdeletio

Externí odkaz: https://doaj.org/article/50a554b06ec24b24a3e04bd0126c1294

Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study

Autor: Therese van Amelsvoort, Michiel L. Houben, Emy S. van der Valk Bouman, Erik Boot, Myrthe A. Nuijts, Emma N. M. M. von Scheibler, Pit Vermeltfoort, Tos T. J. M. Berendschot, Levinus A. Bok, Agnies M. van Eeghen, Noël J.C. Bauer, Michelle B. van Egmond-Ebbeling

Publikováno v: American Journal of Medical Genetics, Part A, 188(2), 569-578. Wiley-Liss Inc.
von Scheibler, E N M M, van der Valk Bouman, E S, Nuijts, M A, Bauer, N J C, Berendschot, T T J M, Vermeltfoort, P, Bok, L A, van Eeghen, A M, Houben, M L, van Amelsvoort, T A M J, Boot, E & van Egmond-Ebbeling, M B 2022, ' Ocular findings in 22q11.2 deletion syndrome : A systematic literature review and results of a Dutch multicenter study ', American Journal of Medical Genetics, Part A, vol. 188, no. 2, pp. 569-578 . https://doi.org/10.1002/ajmg.a.62556

The 22q11.2 deletion syndrome (22q11.2DS) is a multisystem disorder with an estimated prevalence of 1:3000 live births. Manifestations show a marked variability in expression and include speech- and language delay, intellectual disability, and neurop

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca9816f5a3fea1d45a2c185c0f867986
https://doi.org/10.1002/ajmg.a.62556

The role of 22q11.2 deletion syndrome in the relationship between congenital heart disease and scoliosis

Autor: Michiel L. Houben, Jelle F. Homans, Tracy Heung, René M. Castelein, Moyo C. Kruyt, Anne S. Bassett, Steven de Reuver, Erwin Oechslin, Donna M. McDonald-McGinn, Candice K. Silversides

Publikováno v: Spine J

BACKGROUND CONTEXT: For over four decades, clinicians and researchers have suggested a relationship between congenital heart disease (CHD) and scoliosis, attributed to either the disease itself or to the long-term effects of cardiac surgery on the im

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb0accaa1782365e2dc5ec2e4a923b1a
https://doi.org/10.1016/j.spinee.2020.01.006