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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1994 1
1995 1
1996 2
1997 1
1998 5
1999 4
2000 7
2002 1
2003 2
2004 3
2005 5
2006 5
2008 3
2009 4
2010 3
2011 3
2012 5
2013 9
2014 7
2015 2
2016 9
2017 4
2018 3
2019 5
2020 5
2021 6
2022 6
2023 8
2024 2

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Publication date

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109 results

Results by year

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Page 1
Antenatal corticosteroids-to-birth interval in preterm birth.
Dehaene I, De Coen K, Oostra A, Decruyenaere J, Roelens K, Smets K. Dehaene I, et al. Among authors: smets k. Acta Clin Belg. 2021 Dec;76(6):433-440. doi: 10.1080/17843286.2020.1758471. Epub 2020 Apr 30. Acta Clin Belg. 2021. PMID: 32352863
Hearing loss and congenital CMV infection: a systematic review.
Goderis J, De Leenheer E, Smets K, Van Hoecke H, Keymeulen A, Dhooge I. Goderis J, et al. Among authors: smets k. Pediatrics. 2014 Nov;134(5):972-82. doi: 10.1542/peds.2014-1173. Pediatrics. 2014. PMID: 25349318 Review.
First line management of prolonged convulsive seizures in children and adults: good practice points.
De Waele L, Boon P, Ceulemans B, Dan B, Jansen A, Legros B, Leroy P, Delmelle F, Ossemann M, De Raedt S, Smets K, Van De Voorde P, Verhelst H, Lagae L; Belgium League against Epilepsy; Belgium Society for Emergengy and Disaster Medicine. De Waele L, et al. Among authors: smets k. Acta Neurol Belg. 2013 Dec;113(4):375-80. doi: 10.1007/s13760-013-0247-x. Epub 2013 Sep 10. Acta Neurol Belg. 2013. PMID: 24019121
Congenital rubella syndrome after maternal reinfection.
Bullens D, Smets K, Vanhaesebrouck P. Bullens D, et al. Among authors: smets k. Clin Pediatr (Phila). 2000 Feb;39(2):113-6. doi: 10.1177/000992280003900207. Clin Pediatr (Phila). 2000. PMID: 10696549 Review. No abstract available.
PRRT2 mutations: exploring the phenotypical boundaries.
Djémié T, Weckhuysen S, Holmgren P, Hardies K, Van Dyck T, Hendrickx R, Schoonjans AS, Van Paesschen W, Jansen AC, De Meirleir L, Selim LA, Girgis MY, Buyse G, Lagae L, Smets K, Smouts I, Claeys KG, Van den Bergh V, Grisar T, Blatt I, Shorer Z, Roelens F, Afawi Z, Helbig I, Ceulemans B, De Jonghe P, Suls A. Djémié T, et al. Among authors: smets k. J Neurol Neurosurg Psychiatry. 2014 Apr;85(4):462-5. doi: 10.1136/jnnp-2013-305122. Epub 2013 Oct 7. J Neurol Neurosurg Psychiatry. 2014. PMID: 24101679
FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.
Rattay TW, Lindig T, Baets J, Smets K, Deconinck T, Söhn AS, Hörtnagel K, Eckstein KN, Wiethoff S, Reichbauer J, Döbler-Neumann M, Krägeloh-Mann I, Auer-Grumbach M, Plecko B, Münchau A, Wilken B, Janauschek M, Giese AK, De Bleecker JL, Ortibus E, Debyser M, Lopez de Munain A, Pujol A, Bassi MT, D'Angelo MG, De Jonghe P, Züchner S, Bauer P, Schöls L, Schüle R. Rattay TW, et al. Among authors: smets k. Brain. 2019 Jun 1;142(6):1561-1572. doi: 10.1093/brain/awz102. Brain. 2019. PMID: 31135052 Free PMC article.
Congenital cytomegalovirus infection registry in flanders: opportunities and pitfalls.
Keymeulen A, De Leenheer E, Goderis J, Dhooge I, Smets K; Flemish Society of Pediatrics’ Neonatology and Perinatal Epidemiology Working Group for cCMV infection. Keymeulen A, et al. Among authors: smets k. Acta Clin Belg. 2021 Jun;76(3):169-176. doi: 10.1080/17843286.2019.1683262. Epub 2019 Oct 23. Acta Clin Belg. 2021. PMID: 31645217
109 results