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

Year Number of Results
1992 1
1994 1
1997 1
1998 1
1999 2
2000 4
2002 2
2003 1
2005 1
2006 2
2007 1
2008 1
2009 2
2010 1
2011 1
2012 3
2013 2
2014 2
2015 1
2016 1
2020 1
2021 1
2022 2
2023 2
2024 0

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34 results

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Page 1
Epidemiology of acute flaccid myelitis in children in the Netherlands, 2014 to 2019.
Helfferich J, de Lange MM, Benschop KS, Jacobs BC, Van Leer-Buter CC, Meijer A, Bakker DP, de Bie E, Braakman HM, Brandsma R, Neuteboom RF, Niks EH, Niermeijer JM, Roelfsema V, Schoenmaker N, Sie LT, Niesters HG, Brouwer OF, Te Wierik MJ. Helfferich J, et al. Among authors: sie lt. Euro Surveill. 2022 Oct;27(42):2200157. doi: 10.2807/1560-7917.ES.2022.27.42.2200157. Euro Surveill. 2022. PMID: 36268734 Free PMC article. Review.
Long-term outcomes for females with early-onset dystrophinopathy.
Houwen-van Opstal SLS, Tak RO, Pelsma M, van den Heuvel FMA, van Duyvenvoorde HA, Cup EHC, Sie LTL, Vles JSH, de Groot IJM, Voermans NC, Willemsen MAAP. Houwen-van Opstal SLS, et al. Among authors: sie ltl. Dev Med Child Neurol. 2023 Aug;65(8):1093-1104. doi: 10.1111/dmcn.15496. Epub 2022 Dec 23. Dev Med Child Neurol. 2023. PMID: 36562406
Pediatric acute flaccid myelitis: Evaluation of diagnostic criteria and differentiation from other causes of acute flaccid paralysis.
Helfferich J, Neuteboom RF, de Lange MMA, Benschop KSM, Van Leer-Buter CC, Meijer A, Bakker DP, de Bie E, Braakman HMH, Brandsma R, Niks EH, Niermeijer JM, Roelfsema V, Schoenmaker N, Sie LT, Niesters HG, Te Wierik MJM, Jacobs BC, Brouwer OF. Helfferich J, et al. Among authors: sie lt. Eur J Paediatr Neurol. 2023 May;44:28-36. doi: 10.1016/j.ejpn.2023.03.002. Epub 2023 Mar 22. Eur J Paediatr Neurol. 2023. PMID: 36996587 Free article.
[Chronic subdural hematoma].
Sie LT, Snijders CJ. Sie LT, et al. Ned Tijdschr Geneeskd. 1992 Dec 5;136(49):2401-4. Ned Tijdschr Geneeskd. 1992. PMID: 1470238 Dutch. No abstract available.
RYR1-related myopathies: a wide spectrum of phenotypes throughout life.
Snoeck M, van Engelen BG, Küsters B, Lammens M, Meijer R, Molenaar JP, Raaphorst J, Verschuuren-Bemelmans CC, Straathof CS, Sie LT, de Coo IF, van der Pol WL, de Visser M, Scheffer H, Treves S, Jungbluth H, Voermans NC, Kamsteeg EJ. Snoeck M, et al. Among authors: sie lt. Eur J Neurol. 2015 Jul;22(7):1094-112. doi: 10.1111/ene.12713. Epub 2015 May 11. Eur J Neurol. 2015. PMID: 25960145
[An infant with unexplained epilepsy].
van Gaal JC, Petru R, Sie LT. van Gaal JC, et al. Among authors: sie lt. Ned Tijdschr Geneeskd. 2010;154:A2420. Ned Tijdschr Geneeskd. 2010. PMID: 21176267 Dutch.
Mutations in TPM2 and congenital fibre type disproportion.
Clarke NF, Waddell LB, Sie LT, van Bon BW, McLean C, Clark D, Kornberg A, Lammens M, North KN. Clarke NF, et al. Among authors: sie lt. Neuromuscul Disord. 2012 Nov;22(11):955-8. doi: 10.1016/j.nmd.2012.06.002. Epub 2012 Jul 24. Neuromuscul Disord. 2012. PMID: 22832343
34 results