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Results by year

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 2

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Search Results

223 results

Results by year

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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.
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.
Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation.
Beijer D, Kim HJ, Guo L, O'Donovan K, Mademan I, Deconinck T, Van Schil K, Fare CM, Drake LE, Ford AF, Kochański A, Kabzińska D, Dubuisson N, Van den Bergh P, Voermans NC, Lemmers RJ, van der Maarel SM, Bonner D, Sampson JB, Wheeler MT, Mehrabyan A, Palmer S, De Jonghe P, Shorter J, Taylor JP, Baets J. Beijer D, et al. Among authors: van der maarel sm. JCI Insight. 2021 Jul 22;6(14):e148363. doi: 10.1172/jci.insight.148363. JCI Insight. 2021. PMID: 34291734 Free PMC article.
[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.
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.
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.
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.
Elevated plasma complement components in facioscapulohumeral dystrophy.
Wong CJ, Wang L, Holers VM, Frazer-Abel A, van der Maarel SM, Tawil R, Statland JM, Tapscott SJ; ReSolve Network. Wong CJ, et al. Among authors: van der maarel sm. Hum Mol Genet. 2022 Jun 4;31(11):1821-1829. doi: 10.1093/hmg/ddab364. Hum Mol Genet. 2022. PMID: 34919696 Free PMC article.
Ophthalmological findings in facioscapulohumeral dystrophy.
Goselink RJM, Schreur V, van Kernebeek CR, Padberg GW, van der Maarel SM, van Engelen BGM, Erasmus CE, Theelen T. Goselink RJM, et al. Among authors: van der maarel sm. Brain Commun. 2019 Oct 11;1(1):fcz023. doi: 10.1093/braincomms/fcz023. eCollection 2019. Brain Commun. 2019. PMID: 32954265 Free PMC article.
223 results