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

Year Number of Results
1959 1
1975 1
1983 2
1985 4
1986 1
1987 4
1988 3
1989 1
1990 3
1991 6
1992 3
1993 4
1994 7
1995 7
1996 8
1997 7
1998 7
1999 10
2000 10
2001 8
2002 11
2003 13
2004 11
2005 12
2006 11
2007 13
2008 25
2009 33
2010 21
2011 18
2012 20
2013 10
2014 18
2015 14
2016 10
2017 9
2018 15
2019 9
2020 8
2021 16
2022 6
2023 11
2024 6

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378 results

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Page 1
Mouse models of fragile X-related disorders.
Willemsen R, Kooy RF. Willemsen R, et al. Dis Model Mech. 2023 Feb 1;16(2):dmm049485. doi: 10.1242/dmm.049485. Epub 2023 Jan 24. Dis Model Mech. 2023. PMID: 36692473 Free PMC article. Review.
Chest pain triage: gut feeling or protocol-based care?
Willemsen RTA, van 't Hof AWJ. Willemsen RTA, et al. Neth Heart J. 2021 Jun;29(6):309-310. doi: 10.1007/s12471-021-01589-0. Epub 2021 May 10. Neth Heart J. 2021. PMID: 33970437 Free PMC article. No abstract available.
[Fragile X syndrome: new therapeutic strategies].
Zeidler S, Dierckx B, Lubbers K, van Eeghen AM, Lincke CR, Kievit JA, Willemsen R, Rietman A. Zeidler S, et al. Among authors: willemsen r. Tijdschr Psychiatr. 2018;60(5):338-342. Tijdschr Psychiatr. 2018. PMID: 29766482 Free article. Review. Dutch.
Biallelic variants in FLII cause pediatric cardiomyopathy by disrupting cardiomyocyte cell adhesion and myofibril organization.
Ruijmbeek CW, Housley F, Idrees H, Housley MP, Pestel J, Keller L, Lai JK, der Linde HCV, Willemsen R, Piesker J, Al-Hassnan ZN, Almesned A, Dalinghaus M, den Bersselaar LMV, van Slegtenhorst MA, Tessadori F, Bakkers J, van Ham TJ, Stainier DY, Verhagen JM, Reischauer S. Ruijmbeek CW, et al. Among authors: willemsen r. JCI Insight. 2023 Sep 8;8(17):e168247. doi: 10.1172/jci.insight.168247. JCI Insight. 2023. PMID: 37561591 Free PMC article.
Translational endpoints in fragile X syndrome.
de Esch CE, Zeidler S, Willemsen R. de Esch CE, et al. Among authors: willemsen r. Neurosci Biobehav Rev. 2014 Oct;46 Pt 2:256-69. doi: 10.1016/j.neubiorev.2013.10.012. Epub 2013 Oct 30. Neurosci Biobehav Rev. 2014. PMID: 24184744 Review.
[Integrated care: a necessity].
Willemsen RTA. Willemsen RTA. Ned Tijdschr Geneeskd. 2020 Nov 23;164:D5077. Ned Tijdschr Geneeskd. 2020. PMID: 33332049 Dutch.
Disruption of TUFT1, a Desmosome-Associated Protein, Causes Skin Fragility, Woolly Hair, and Palmoplantar Keratoderma.
Verkerk AJMH, Andrei D, Vermeer MCSC, Kramer D, Schouten M, Arp P, Verlouw JAM, Pas HH, Meijer HJ, van der Molen M, Oberdorf-Maass S, Nijenhuis M, Romero-Herrera PH, Hoes MF, Bremer J, Slotman JA, van den Akker PC, Diercks GFH, Giepmans BNG, Stoop H, Saris JJ, van den Ouweland AMW, Willemsen R, Hublin JJ, Dean MC, Hoogeboom AJM, Silljé HHW, Uitterlinden AG, van der Meer P, Bolling MC. Verkerk AJMH, et al. Among authors: willemsen r. J Invest Dermatol. 2024 Feb;144(2):284-295.e16. doi: 10.1016/j.jid.2023.02.044. Epub 2023 Sep 15. J Invest Dermatol. 2024. PMID: 37716648 Free article.
FMR1: a gene with three faces.
Oostra BA, Willemsen R. Oostra BA, et al. Among authors: willemsen r. Biochim Biophys Acta. 2009 Jun;1790(6):467-77. doi: 10.1016/j.bbagen.2009.02.007. Epub 2009 Feb 21. Biochim Biophys Acta. 2009. PMID: 19233246 Free PMC article. Review.
Key features of puberty onset and progression can help distinguish self-limited delayed puberty from congenital hypogonadotrophic hypogonadism.
Aung Y, Kokotsis V, Yin KN, Banerjee K, Butler G, Dattani MT, Dimitri P, Dunkel L, Hughes C, McGuigan M, Korbonits M, Paltoglou G, Sakka S, Shah P, Storr HL, Willemsen RH, Howard SR. Aung Y, et al. Among authors: willemsen rh. Front Endocrinol (Lausanne). 2023 Aug 28;14:1226839. doi: 10.3389/fendo.2023.1226839. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37701896 Free PMC article.
378 results