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

Year Number of Results
1992 1
1994 2
1995 4
1996 1
1998 1
1999 2
2000 2
2001 3
2002 3
2003 8
2004 10
2005 7
2006 9
2007 8
2008 4
2009 8
2010 11
2011 16
2012 17
2013 16
2014 12
2015 19
2016 14
2017 8
2018 17
2019 14
2020 13
2021 11
2022 6
2023 8
2024 3

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232 results

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Page 1
Facioscapulohumeral muscular dystrophy: the road to targeted therapies.
Tihaya MS, Mul K, Balog J, de Greef JC, Tapscott SJ, Tawil R, Statland JM, van der Maarel SM. Tihaya MS, et al. Among authors: van der maarel sm. Nat Rev Neurol. 2023 Feb;19(2):91-108. doi: 10.1038/s41582-022-00762-2. Epub 2023 Jan 10. Nat Rev Neurol. 2023. PMID: 36627512 Review.
Facioscapulohumeral muscular dystrophy.
van der Maarel SM, Frants RR, Padberg GW. van der Maarel SM, et al. Biochim Biophys Acta. 2007 Feb;1772(2):186-94. doi: 10.1016/j.bbadis.2006.05.009. Epub 2006 Jun 6. Biochim Biophys Acta. 2007. PMID: 16837171 Free article. Review.
[Facioscapulohumeral muscular dystrophy].
Wilbers J, Frants RR, van Engelen BG, Padberg GW, van der Maarel SM. Wilbers J, et al. Among authors: van der maarel sm. Ned Tijdschr Tandheelkd. 2010 Jan;117(1):11-4. Ned Tijdschr Tandheelkd. 2010. PMID: 20180344 Free article. Review. Dutch.
Genetic and epigenetic contributors to FSHD.
Daxinger L, Tapscott SJ, van der Maarel SM. Daxinger L, et al. Among authors: van der maarel sm. Curr Opin Genet Dev. 2015 Aug;33:56-61. doi: 10.1016/j.gde.2015.08.007. Epub 2015 Sep 7. Curr Opin Genet Dev. 2015. PMID: 26356006 Free PMC article. Review.
Facioscapulohumeral muscular dystrophy.
Tawil R, Van Der Maarel SM. Tawil R, et al. Among authors: van der maarel sm. Muscle Nerve. 2006 Jul;34(1):1-15. doi: 10.1002/mus.20522. Muscle Nerve. 2006. PMID: 16508966 Review.
p53 convergently activates Dux/DUX4 in embryonic stem cells and in facioscapulohumeral muscular dystrophy cell models.
Grow EJ, Weaver BD, Smith CM, Guo J, Stein P, Shadle SC, Hendrickson PG, Johnson NE, Butterfield RJ, Menafra R, Kloet SL, van der Maarel SM, Williams CJ, Cairns BR. Grow EJ, et al. Among authors: van der maarel sm. Nat Genet. 2021 Aug;53(8):1207-1220. doi: 10.1038/s41588-021-00893-0. Epub 2021 Jul 15. Nat Genet. 2021. PMID: 34267371 Free PMC article.
Systemic delivery of a DUX4-targeting antisense oligonucleotide to treat facioscapulohumeral muscular dystrophy.
Bouwman LF, den Hamer B, van den Heuvel A, Franken M, Jackson M, Dwyer CA, Tapscott SJ, Rigo F, van der Maarel SM, de Greef JC. Bouwman LF, et al. Among authors: van der maarel sm. Mol Ther Nucleic Acids. 2021 Sep 27;26:813-827. doi: 10.1016/j.omtn.2021.09.010. eCollection 2021 Dec 3. Mol Ther Nucleic Acids. 2021. PMID: 34729250 Free PMC article.
IgG4-mediated autoimmune diseases: a niche of antibody-mediated disorders.
Huijbers MG, Plomp JJ, van der Maarel SM, Verschuuren JJ. Huijbers MG, et al. Among authors: van der maarel sm. Ann N Y Acad Sci. 2018 Feb;1413(1):92-103. doi: 10.1111/nyas.13561. Epub 2018 Jan 28. Ann N Y Acad Sci. 2018. PMID: 29377160 Free PMC article. Review.
Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkers.
van den Heuvel A, Lassche S, Mul K, Greco A, San León Granado D, Heerschap A, Küsters B, Tapscott SJ, Voermans NC, van Engelen BGM, van der Maarel SM. van den Heuvel A, et al. Among authors: van der maarel sm. Sci Rep. 2022 Jan 26;12(1):1426. doi: 10.1038/s41598-022-04817-8. Sci Rep. 2022. PMID: 35082321 Free PMC article.
232 results