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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 6
2013 11
2014 8
2015 6
2016 11
2017 5
2018 3
2019 5
2020 5
2021 6
2022 6
2023 8
2024 5

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121 results

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Page 1
The External Genitalia Score (EGS): A European Multicenter Validation Study.
van der Straaten S, Springer A, Zecic A, Hebenstreit D, Tonnhofer U, Gawlik A, Baumert M, Szeliga K, Debulpaep S, Desloovere A, Tack L, Smets K, Wasniewska M, Corica D, Calafiore M, Ljubicic ML, Busch AS, Juul A, Nordenström A, Sigurdsson J, Flück CE, Haamberg T, Graf S, Hannema SE, Wolffenbuttel KP, Hiort O, Ahmed SF, Cools M. van der Straaten S, et al. Among authors: smets k. J Clin Endocrinol Metab. 2020 Mar 1;105(3):dgz142. doi: 10.1210/clinem/dgz142. J Clin Endocrinol Metab. 2020. PMID: 31665438 Free article.
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
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.
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
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
Investigation of GRIN2A in common epilepsy phenotypes.
Lal D, Steinbrücker S, Schubert J, Sander T, Becker F, Weber Y, Lerche H, Thiele H, Krause R, Lehesjoki AE, Nürnberg P, Palotie A, Neubauer BA, Muhle H, Stephani U, Helbig I, Becker AJ, Schoch S, Hansen J, Dorn T, Hohl C, Lüscher N; Epicure consortium; EuroEPINOMICS-CoGIE consortium; von Spiczak S, Lemke JR. Lal D, et al. Epilepsy Res. 2015 Sep;115:95-9. doi: 10.1016/j.eplepsyres.2015.05.010. Epub 2015 Jun 2. Epilepsy Res. 2015. PMID: 26220384
121 results